	This product is intended for use in the control of the Randox Total Antioxidant Status assay, "TOTAL ANTIOXIDANT STATUS (TAS CONTROL)" - NX2331
	This product is intended for in vitro diagnostic use in the quality control of serum on clinical chemistry systems. ABAXIS CHEMISTRY CONTROL LEVEL 1 - 1100-9131E
	This product is intended for in vitro diagnostic use in the quality control of serum on clinical chemistry ABAXIS CHEMISTRY CONTROL LEVEL 2 - 1100-9132E
	The paracetamol test system is intended for the quantitative in vitro determination of Acetaminophen in human serum. ACE - ACE4023
	ACID PHOSPHATASE (ACP) ACID PHOSPHATASE (ACP) - AC8001
	Acid Wash Solution should be used in conjunction with reagents to clean probes and cuvettes ACID WASH SOLUTION (WASH SOLN. 3) - RX8129
	The acid phosphatase test system is intended for the quantitative in vitro determination of Acid Phosphatase in serum. ACP - AC1011
	The Active Vitamin B12 Control Level 1 is intended for use with in vitro diagnostic assays for the quantitative determination of active Vitamin B12 (Holotranscobalamin/HoloTC) in human serum and plasma. The Active Vitamin B12 Control Level 1 is assayed with target values and are suitable for use on various analysers. The Active Vitamin B12 Control Level 1 is for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation. ACTIVE VITAMIN B12 CONTROL LEVEL 1 - VB10524
	The Active Vitamin B12 Control Level 2 is intended for use with in vitro diagnostic assays for the quantitative determination of active Vitamin B12 (Holotranscobalamin/HoloTC) in human serum and plasma. The Active Vitamin B12 Control Level 2 is assayed with target values and are suitable for use on various analysers. The Active Vitamin B12 Control Level 2 is for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation. ACTIVE VITAMIN B12 CONTROL LEVEL 2 - VB10525
	ADIPONECTIN CALIBRATOR (ADPN CAL) ADIPONECTIN CALIBRATOR (ADPN CAL) - AO2800
	ADIPONECTIN CONTROL - LEVEL 2 (ADPN CONTROL 2) ADIPONECTIN CONTROL - LEVEL 2 (ADPN CONTROL 2) - AO2801
	ADIPONECTIN CONTROL - LEVEL 3 (ADPN CONTROL 3) ADIPONECTIN CONTROL - LEVEL 3 (ADPN CONTROL 3) - AO2802
	ALANINE AMINOTRANSFERASE (ALT) ALANINE AMINOTRANSFERASE (ALT) - AL100
	ALANINE AMINOTRANSFERASE (ALT) ALANINE AMINOTRANSFERASE (ALT) - AL1200
	ALANINE AMINOTRANSFERASE (ALT) ALANINE AMINOTRANSFERASE (ALT) - AL1205
	ALANINE AMINOTRANSFERASE (ALT) ALANINE AMINOTRANSFERASE (ALT) - AL1268
	ALANINE AMINOTRANSFERASE (ALT) ALANINE AMINOTRANSFERASE (ALT) - AL146
	ALANINE AMINOTRANSFERASE (ALT) ALANINE AMINOTRANSFERASE (ALT) - AL2360
	ALANINE AMINOTRANSFERASE (ALT) ALANINE AMINOTRANSFERASE (ALT) - AL7904
	ALANINE AMINOTRANSFERASE (ALT) ALANINE AMINOTRANSFERASE (ALT) - AL7930
	ALANINE AMINOTRANSFERASE (ALT) ALANINE AMINOTRANSFERASE (ALT) - AL8006
	ALANINE AMINOTRANSFERASE (ALT) ALANINE AMINOTRANSFERASE (ALT) - AL8304
	An Albumin test system is a device intended for the quantitative in vitro determination of Albumin concentration in serum and plasma. ALB - AB362
	An Albumin test system is a device intended for the quantitative in vitro determination of Albumin concentration in serum and plasma. ALB - AB3800
	An Albumin test system is a device intended for the quantitative in vitro determination of Albumin concentration in serum. ALB - AB8301
	ALDOLASE (ALS) ALDOLASE (ALS) - AD189
	ALDOLASE LEVEL 2 CONTROL (ALS CONTROL 2) ALDOLASE LEVEL 2 CONTROL (ALS CONTROL 2) - AD5001
	ALDOLASE LEVEL 3 CONTROL (ALS CONTROL 3) ALDOLASE LEVEL 3 CONTROL (ALS CONTROL 3) - AD5002
	Alkaline Detergent is used for cleaning the instrument probe and reaction cuvettes. ALKALINE DETERGENT (Alkaline Detergent) - RX8108
	ALKALINE PHOSPHATASE (ALP) ALKALINE PHOSPHATASE (ALP) - AP8302
	Alkaline Wash Solution should be used in conjunction with reagents to clean cuvettes ALKALINE WASH SOLUTION (WASH soln. 9) - RX8130
	An Alkaline Phosphatase test system is a device intended for the quantitative in vitro determination of Alkaline Phosphatase (ALP) activity in serum or plasma. ALP - AP311
	An Alkaline Phosphatase test system is a device intended for the quantitative in vitro determination of Alkaline Phosphatase (ALP) activity in serum or plasma. ALP - AP313
	An Alkaline Phosphatase test system is a device intended for the quantitative in vitro determination of Alkaline Phosphatase (ALP) activity in serum or plasma. ALP - AP3802
	An Alkaline Phosphatase test system is a device intended for the quantitative in vitro determination of Alkaline Phosphatase (ALP) activity in serum or plasma. ALP - AP3877
	An Alkaline Phosphatase test system is a device intended for the quantitative in vitro determination of Alkaline Phosphatase (ALP) activity in serum or plasma. ALP - AP7927
	The ALP method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of Alkaline Phosphatase (ALP) activity in serum or plasma. ALP - AP2809
	ALPHA-1-ACID-GLYCOPROTEIN (AGT) ALPHA-1-ACID-GLYCOPROTEIN (AGT) - AG2472
	The Aldolase Calibration Serum is intended for in vitro diagnostic use, in the calibration of the Aldolase assay AD189. ALS CAL - AD5000
	An ALT test system is a device intended for the quantitative in vitro determination of Alanine Aminotransferase (ALT) activity in serum and plasma. ALT - AL3801
	An ALT test system is a device intended for the quantitative in vitro determination of of Alanine Aminotransferase (ALT) activity in serum and plasma. ALT - AL3875
	The AMH Control Level 1 (AMH10509) is intended for use with in vitro diagnostic assays for the quantitative determination of Anti-Müllerian Hormone in human serum and plasma. The AMH Control Level 1 (AMH10509) is assayed with target values and is suitable for use on automated analysers.The AMH Control Level 1 (AMH10509) is for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation. AMH CONTROL LEVEL 1 (AMH CONTROL 1) - AMH10509
	The AMH Control Level 2 (AMH10514) is intended for use with in vitro diagnostic assays for the quantitative determination of Anti-Müllerian Hormone in human serum and plasma. The AMH Control Level 2 (AMH10514) is assayed with target values and is suitable for use on automated analysers.The AMH Control Level 2 (AMH10514) is for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation. AMH CONTROL LEVEL 2 (AMH CONTROL 2) - AMH10514
	The AMH Control Level 3 (AMH10515) is intended for use with in vitro diagnostic assays for the quantitative determination of Anti-Müllerian Hormone in human serum and plasma. The AMH Control Level 3 (AMH10515) is assayed with target values and is suitable for use on automated analysers.The AMH Control Level 3 (AMH10515) is for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation. AMH CONTROL LEVEL 3 (AMH CONTROL 3) - AMH10515
	The AMH Control Level 4 (AMH10516) is intended for use with in vitro diagnostic assays for the quantitative determination of Anti-Müllerian Hormone in human serum and plasma. The AMH Control Level 4 (AMH10516) is assayed with target values and is suitable for use on automated analysers.The AMH Control Level 4 (AMH10516) is for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation. AMH CONTROL LEVEL 4 (AMH CONTROL 4) - AMH10516
	AMMONIA (NH3) AMMONIA (NH3) - AM1015
	AMMONIA (NH3) AMMONIA (NH3) - AM1054
	The Randox Ammonia Ethanol Control Level 1 is intended for in vitro diagnostic use, in the quality control of Ammonia and Alcohol Assays to monitor precision and to detect systematic analytical deviations on clinical chemistry systems. AMMONIA ETHANOL CONTROL - LEVEL 1 (NH3/EtOH CONTROL 1) - EA1366
	The Randox Ammonia Ethanol Control - Level 2 is intended for in vitro diagnostic use, in the quality control of Ammonia and Alcohol Assays to monitor precision and to detect systematic analytical deviations on clinical chemistry systems. AMMONIA ETHANOL CONTROL - LEVEL 2 (NH3/EtOH CONTROL 2) - EA1367
	The Randox Ammonia Ethanol Control - Level 3 is intended for in vitro diagnostic use, in the quality control of Ammonia and Alcohol Assays to monitor precision and to detect systematic analytical deviations on clinical chemistry systems. AMMONIA ETHANOL CONTROL - LEVEL 3 (NH3/EtOH CONTROL 3) - EA1368
	An α-amylase test system is a device intended for the quantitative in vitro determination of α-amylase activity in serum, or urine. AMY - AY7932
	An α-amylase test system is a device intended for the quantitative in vitro determination of α-amylase activity in serum, plasma or urine. AMY - AY3805
	An α-amylase test system is a device intended for the quantitative in vitro determination of α-amylase activity in serum, plasma or urine. AMY - AY7931
	An α-amylase test system is a device intended for the quantitative in vitro determination of α-amylase activity in serum, plasma or urine. AMY - AY9707
	The AMY method used on the Dimension® clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of amylase activity in serum, plasma and urine. AMY - AY2811
	The amylase test system is intended for the quantitative in vitro determination of Amylase in serum, plasma or urine. AMY - AY1580
	The amylase test system is intended for the quantitative in vitro determination of Amylase in serum, plasma or urine. AMY - AY1582
	Antibacterial Detergent is used for cleaning the instrument probe and reaction cuvettes. ANTI-BACTERIAL DETERGENT (Detergent) - RX8106
	Anti-Streptolysin O (ASO) Anti-Streptolysin O (ASO) - LO2715
	ANTI-STREPTOLYSIN O STANDARD (ASO STD) ANTI-STREPTOLYSIN O STANDARD (ASO STD) - LO2306
	ANTI-STREPTOLYSIN-O 2 (ASO 2) ANTI-STREPTOLYSIN-O 2 (ASO 2) - LO3998
	ANTI-STREPTOLYSIN-O 2 (ASO 2) ANTI-STREPTOLYSIN-O 2 (ASO 2) - LO3999
	ANTI-STREPTOLYSIN-O 2 (ASO 2) ANTI-STREPTOLYSIN-O 2 (ASO 2) - LO8015
	ANTI-STREPTOLYSIN-O 2 (ASO 2) ANTI-STREPTOLYSIN-O 2 (ASO 2) - LO8305
	Intended for the quantitative in vitro determination of Apolipoprotein A-I (APO A-I) in serum and plasma APO A-I - LP2116
	Intended for the quantitative in vitro determination of Apolipoprotein A-I (APO A-I) in serum and plasma APO A-I - LP2866
	Intended for the quantitative in vitro determination of Apolipoprotein A-I (APO A-I) in serum and plasma APO A-I - LP2989
	Intended for the quantitative in vitro determination of Apolipoprotein A-I (APO A-I) in serum and plasma APO A-I - LP3838
	An APO B test system is a device intended for the quantitative in vitro determination of Apolipoprotein B (APO B) in serum and plasma. APO B - LP2117
	An APO B test system is a device intended for the quantitative in vitro determination of Apolipoprotein B (APO B) in serum and plasma. APO B - LP2990
	An APO B test system is a device intended for the quantitative in vitro determination of Apolipoprotein B (APO B) in serum and plasma. APO B - LP3839
	Immunoturbidimetric assay for the quantitative in vitro determination of Apolipoprotein B in human serum. APO B - LP2867
	This product is intended for in-vitro use in the calibration of Apolipoprotein A-I and Apolipoprotein B assays. APO CAL - LP3023
	Apolipoprotein A1 & B Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of Beckman Coulter AU Systems for Apolipoprotein A1 and Apolipoprotein B. APOLIPOPROTEIN A1 & B LINEARITY VERIFIERS (For Beckman Coulter AU Systems) - LV10363
	Apo Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of Roche Systems for Apo A1 and Apo B. APOLIPOPROTEIN A1 & B LINEARITY VERIFIERS (For Roche Systems) (ApoLV-R) - LV10357
	APOLIPOPROTEIN A-I (APO A-I) APOLIPOPROTEIN A-I (APO A-I) - LP8007
	APOLIPOPROTEIN A-II (APO A-II) APOLIPOPROTEIN A-II (APO A-II) - LP3867
	APOLIPOPROTEIN B (APO B) APOLIPOPROTEIN B (APO B) - LP8008
	APOLIPOPROTEIN CALIBRATOR 2 (APO CAL 2) APOLIPOPROTEIN CALIBRATOR 2 (APO CAL 2) - LP5047
	APOLIPOPROTEIN C-II (APO C-II) APOLIPOPROTEIN C-II (APO C-II) - LP3866
	APOLIPOPROTEIN C-III (APO C-III) APOLIPOPROTEIN C-III (APO C-III) - LP3865
	APOLIPOPROTEIN CONTROL - LEVEL 1 (APO CONTROL 1) APOLIPOPROTEIN CONTROL - LEVEL 1 (APO CONTROL 1) - LE5016
	APOLIPOPROTEIN CONTROL - LEVEL 2 (APO CONTROL 2) APOLIPOPROTEIN CONTROL - LEVEL 2 (APO CONTROL 2) - LE5017
	APOLIPOPROTEIN CONTROL - LEVEL 3 (APO CONTROL 3) APOLIPOPROTEIN CONTROL - LEVEL 3 (APO CONTROL 3) - LE5018
	APOLIPOPROTEIN E (APO E) APOLIPOPROTEIN E (APO E) - LP3864
	ASPARTATE AMINOTRANSFERASE (AST) ASPARTATE AMINOTRANSFERASE (AST) - AS101
	ASPARTATE AMINOTRANSFERASE (AST) ASPARTATE AMINOTRANSFERASE (AST) - AS147
	ASPARTATE AMINOTRANSFERASE (AST) ASPARTATE AMINOTRANSFERASE (AST) - AS8005
	ASSAYED BOVINE MULTI SERA - LEVEL 1 (BOV ASY CONTROL 1) ASSAYED BOVINE MULTI SERA - LEVEL 1 (BOV ASY CONTROL 1) - AL1027
	ASSAYED BOVINE MULTI SERA - LEVEL 2 (BOV ASY CONTROL 2) ASSAYED BOVINE MULTI SERA - LEVEL 2 (BOV ASY CONTROL 2) - AN1026
	ASSAYED BOVINE MULTI SERA - LEVEL 3 (BOV ASY CONTROL 3) ASSAYED BOVINE MULTI SERA - LEVEL 3 (BOV ASY CONTROL 3) - AE1032
	ASSAYED URINE CONTROL - LEVEL 2 (URN ASY CONTROL 2) ASSAYED URINE CONTROL - LEVEL 2 (URN ASY CONTROL 2) - AU2352
	ASSAYED URINE CONTROL - LEVEL 3 (URN ASY CONTROL 3) ASSAYED URINE CONTROL - LEVEL 3 (URN ASY CONTROL 3) - AU2353
	The AST method used on the Dimension® clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of aspartate aminotransferase activity in serum or plasma. AST - AS2800
	The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma. AST - AS1202
	The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma. AST - AS1204
	The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma. AST - AS1267
	The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma. AST - AS2359
	The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma. AST - AS3804
	The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma. AST - AS3876
	The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma. AST - AS7905
	The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma. AST - AS7938
	The AST test system is intended for the quantitative in vitro determination of Aspartate Aminotransferase (AST) in serum or plasma. AST - AS8306
	This product should be used in conjunction with RX daytona plus reagents to clean probes and cuvettes. AWS - WS8397
	This product should be used in conjunction with RX SERIES reagents to clean probes and cuvettes. AWS - WS3853
	B2Microglobulin (B2M) B2Microglobulin (B2M) - BM3887
	B2Microglobulin (B2M) B2Microglobulin (B2M) - BM8016
	The Barbiturates assay is an in vitro diagnostic test for the qualitative and semi-quantitative detection of Barbiturates in human urine. BARB - DA4008
	The Benzodiazepine assay is an in vitro diagnostic test for the qualitative and semi-quantitative detection of Benzodiazepines in human urine BENZ - DA4009
	The Randox Benzodiazepines Calibrator Set is intended for use in the calibration of the Benzodiazepines assay. The Calibrator Set contains 5 levels of calibrator containing the specific drug Oxazepam. BENZ CAL - DA3129
	The Randox Benzodiazepines Control Level 1 is intended for use in the Quality Control of the Benzodiazepines (BENZ) assay. The Benzodiazepine Control Level 1 contains the specific drug Oxazepam. BENZ CONTROL 1 - DA3130
	The Randox Benzodiazepines Control Level 2 is intended for use in the Quality Control of the Benzodiazepines (BENZ) assay. The Benzodiazepine Control Level 2 contains the specific drug Oxazepam. BENZ CONTROL 2 - DA3131
	BETA 2 MICROGLOBULIN CALIBRATOR (B2M CAL) BETA 2 MICROGLOBULIN CALIBRATOR (B2M CAL) - BM1362
	The device is intended for the quantitative in vitro determination of total and direct bilirubin in serum or plasma. BIL - BR411
	The device is intended for the quantitative in vitro determination of total and direct bilirubin in serum or plasma. BIL - BR412
	BILIRUBIN ELEVATED SERUM (BIL CONTROL H) BILIRUBIN ELEVATED SERUM (BIL CONTROL H) - BE454
	Bilirubin Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of Roche Systems for Total and Direct Bilirubin. BILIRUBIN LINEARITY VERIFIER (For Roche Systems) (BILIRUBIN LIN VER ROCHE) - LV10356
	BLOOD GAS CONTROL - LEVEL 1 (BG CONTROL 1) BLOOD GAS CONTROL - LEVEL 1 (BG CONTROL 1) - BG5001
	BLOOD GAS CONTROL - LEVEL 2 (BG CONTROL 2) BLOOD GAS CONTROL - LEVEL 2 (BG CONTROL 2) - BG5002
	BLOOD GAS CONTROL - LEVEL 3 (BG CONTROL 3) BLOOD GAS CONTROL - LEVEL 3 (BG CONTROL 3) - BG5003
	The BNP Controls for Abbott (CQ10521) are intended for use with in vitro diagnostic assays for the quantitative determination of BNP in human serum and plasma. The BNP Controls for Abbott (CQ10521) are assayed with target values and are suitable for use on Abbott analysers. The BNP Controls for Abbott (CQ10521) are for use by trainedlaboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation. BNP CONTROLS FOR ABBOTT (BNP CONTROL) - CQ10521
	The BNP Controls for Beckman (CQ10520) are intended for use with in vitro diagnostic assays for the quantitative determination of BNP in human serum and plasma. The BNP Controls for Beckman (CQ10520) are assayed with target values and are suitable for use on Beckman analysers. The BNP Controls for Beckman (CQ10520) are for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation. BNP CONTROLS FOR BECKMAN (BNP CONTROL) - CQ10520
	BOVINE PRECISION MULTI SERA - LEVEL 1 (BOV PREC CONTROL 1) BOVINE PRECISION MULTI SERA - LEVEL 1 (BOV PREC CONTROL 1) - SL1084
	BOVINE PRECISION MULTI SERA - LEVEL 2 (BOV PREC CONTROL 2) BOVINE PRECISION MULTI SERA - LEVEL 2 (BOV PREC CONTROL 2) - SN1085
	BOVINE PRECISION MULTI SERA - LEVEL 3 (BOV PREC CONTROL 3) BOVINE PRECISION MULTI SERA - LEVEL 3 (BOV PREC CONTROL 3) - SE1086
	Diluted wash buffer is used for washing the biochips between assay steps to remove all unbound materials. BUF WASH (conc.) - EV3581
	The BUN method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of urea nitrogen in serum, plasma and urine. BUN - UR2821
	BUTYRYL CHOLINESTERASE (CHE) BUTYRYL CHOLINESTERASE (CHE) - CE190
	BUTYRYL CHOLINESTERASE (CHE) BUTYRYL CHOLINESTERASE (CHE) - CE7944
	The Cocaine assay is an in vitro diagnostic test for the qualitative and semi-quantitative detection of benzoylecgonine (Cocaine Metabolite) in human urine. BZG - DA4011
	This product is a weak bleach solution. C1 SOLUTION (C1 SOLN) - RX8143
	A Complement C3 test system is a device intended for the quantitative in vitro determination of Complement C3 concentration in serum C3 - CM3845
	A Complement C4 test system is a device intended for the quantitative in vitro determination of Complement C4 concentration in serum C4 - CM3846
	The calcium method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of calcium concentration in serum. Ca - CA2807
	The calcium test system is a device intended for the quantitative in vitro determination of calcium concentration in serum, plasma or urine Ca - CA3871
	The calcium test system is a device intended for the quantitative in vitro determination of calcium concentration in serum, plasma or urine Ca - CA7941
	The calcium test system is a device intended for the quantitative in vitro determination of calcium in serum, plasma or urine Ca - CA590
	The device is intended for use as a calibrator in clinical chemistry assays. Randox calibration sera are based on lyophilized human serum. The concentrations and activities are suitable for calibration of clinical chemistry assays on a wide range of automatic analyzers. CAL 2 - CAL2350
	The device is intended for use as a calibrator in clinical chemistry assays. Randox calibration sera are based on lyophilized human serum. The concentrations and activities are suitable for calibration of clinical chemistry assays on a wide range of automatic analyzers. CAL 3 - CAL2351
	The product is intended to be used as a wash solution and single point calibrator. Calibrator A is pumped into the sample port by the Calibrator A pump and then positioned in front of the sensor. CAL A - RX4000
	The product is intended to be used as a second Calibrator in a two-point calibration. Calibrator B is aspirated from a sample cup at position 18 on the analyser ASP tray at least once every 8 hours depending on the laboratories schedule. CAL B - RX3949
	CALCIUM (Ca) CALCIUM (Ca) - CA8309
	The calcium test system is a device intended for the quantitative in vitro determination of calcium concentration in serum, plasma or urine Calcium (Ca) - CA2390
	This product is intended for in vitro use, in the quality control of Cardiac Markers on clinical chemistry and Immunoassay systems. CARDIAC CONTROL - LEVEL 1 (CRD CONTROL 1) - CQ10429
	This product is intended for in vitro use, in the quality control of Cardiac Markers on clinical chemistry and Immunoassay systems. CARDIAC CONTROL - LEVEL 2 (CRD CONTROL 2) - CQ10430
	This product is intended for in vitro use, in the quality control of Cardiac Markers on clinical chemistry and Immunoassay systems. CARDIAC CONTROL - LEVEL 3 (CRD CONTROL 3) - CQ10431
	This product is intended for intended for use with in vitro diagnostic assays, for the quantitative determination of Troponin I. Cardiac Controls are unassayed without target values and are suitable for use on automated analysers. Cardiac Controls are for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation. CARDIAC ULTRA LOW CONTROL (CRD CONTROL Ultra Low) - CQ10428
	For the quantitative in vitro determination of Carbamazepine in human serum CBZ - TD3416
	CERULOPLASMIN (CPL) CERULOPLASMIN (CPL) - CPL4017
	CHEMISTRY PREMIUM - LEVEL 2 (CHEM PREMIUM 2) CHEMISTRY PREMIUM - LEVEL 2 (CHEM PREMIUM 2) - HN5067
	CHEMISTRY PREMIUM - LEVEL 3 (CHEM PREMIUM 3) CHEMISTRY PREMIUM - LEVEL 3 (CHEM PREMIUM 3) - HE5068
	For the quantitative in vitro determination of cholesterol in serum and plasma. CHOL - CH3810
	CHOLESTEROL (CHOL) CHOLESTEROL (CHOL) - CH8019
	For the quantitative in vitro determination of Cholesterol in serum and plasma. CHOLESTEROL (CHOL) - CH200
	For the quantitative in vitro determination of cholesterol in serum and plasma. CHOLESTEROL (CHOL) - CH8310
	The CK method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of creatine kinase activity in serum or plasma. CK - CK2813
	The device is intended for the quantitative in vitro determination of creatine kinase in serum or plasma. CK NAC - CK110
	The device is intended for the quantitative in vitro determination of creatine kinase in serum or plasma. CK NAC - CK113
	The device is intended for the quantitative in vitro determination of creatine kinase in serum or plasma. CK NAC - CK335
	The device is intended for the quantitative in vitro determination of creatine kinase in serum or plasma. CK NAC - CK3812
	The device is intended for the quantitative in vitro determination of creatine kinase in serum or plasma. CK NAC - CK3878
	The device is intended for the quantitative in vitro determination of creatine kinase in serum or plasma. CK NAC - CK522
	The device is intended for the quantitative in vitro determination of CK-MB concentration in serum or plasma. CK-MB - CK1296
	The device is intended for the quantitative in vitro determination of CK-MB concentration in serum or plasma. CK-MB - CK1553
	The device is intended for the quantitative in vitro determination of CK-MB concentration in serum or plasma. CK-MB - CK4043
	The device is intended for use in the calibration of CK-MB assays in clinical chemistry systems. CK-MB CAL - CK2393
	The device is intended for use in the quality control of CK-MB assays on clinical chemistry systems. CK-MB CONTROL - CK1212
	The device is intended for the quantitative in vitro determination of creatine kinase activity in serum or plasma. CK-NAC - CK7947
	Cleaning Solution for the RX series analysers Cl SOLN - RX3973
	Clinical Chemistry Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of the Roche Systems for Albumin, BUN, Calcium, Total Cholesterol, Creatinine, Glucose, Lactate, Lithium, Magnesium, Phosphate, Total Protein, Triglycerides, Uric acid, Iron, Sodium, Potassium and Chloride assays. CLINICAL CHEMISTRY LINEARITY VERIFIERS (For Roche Systems) - LV10390
	The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma. CO2 - CD116
	The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma. CO2 - CD127
	The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma. CO2 - CD129
	The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma. CO2 - CD7942
	CO2/Electrolyte Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of the Roche Systems for Carbon Dioxide, Sodium, Potassium, and Chloride. CO2/ELECTROLYTE LINEARITY VERIFIERS (For Roche Systems) (CO2 LIN VER) - LV10362
	COAGULATION CALIBRATOR (COAG CAL) COAGULATION CALIBRATOR (COAG CAL) - CG5037
	COAGULATION CONTROL - LEVEL 1 (COAG CONTROL 1) COAGULATION CONTROL - LEVEL 1 (COAG CONTROL 1) - CG5021
	COAGULATION CONTROL - LEVEL 2 (COAG CONTROL 2) COAGULATION CONTROL - LEVEL 2 (COAG CONTROL 2) - CG5022
	COAGULATION CONTROL - LEVEL 3 (COAG CONTROL 3) COAGULATION CONTROL - LEVEL 3 (COAG CONTROL 3) - CG5023
	The Randox ConcizuTrace™ sample collection kit is used for the collection and transportation of blood samples, taken by a trained phlebotomist. The samples will be transported to a professional laboratory for testing using either the ConcizuTrace™ ELISA kit or Concizumab ELISA kit. ConcizuTrace™ Sample Collection Kit - CZM10596
	COPPER (Cu) COPPER (Cu) - CU2340
	The CREA method used on the Dimension clinical chemistry system is an in vitro diagnostic device intended for the quantitative determination of Creatinine in serum, plasma or urine CREA - CR2804
	The device intended for the quantitative in vitro determination of Creatinine in serum, plasma or urine CREA - CR524
	The is intended for the quantitative in vitro diagnostic determination of Creatinine in serum, plasma or urine CREA - CR3814
	The is intended for the quantitative in vitro diagnostic determination of Creatinine in serum, plasma or urine CREA - CR7948
	The is intended for the quantitative in vitro diagnostic determination of Creatinine in serum, plasma or urine CREA - CR8316
	C-Reactive Protein Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of Roche Systems for C-reactive protein (CRP). C-REACTIVE PROTEIN LINEARITY VERIFIERS (For Roche Series) (CPLV) - LV10334
	CREATININE (CREA) CREATININE (CREA) - CR510
	The CRP test system is intended for the quantitative in vitro determination of CRP concentration in serum. CRP - CP3826
	The CRP test system is intended for the quantitative in vitro determination of CRP concentration in serum. CRP - CP7950
	The CRP test system is intended for the quantitative in vitro determination of CRP concentration in serum. CRP - CP9742
	The device is a latex agglutination slide test intended for qualitative and semi-quantitative in vitro diagnostic determination of C-Reactive Protein (CRP) concentration in serum. CRP - CP1423
	The device is a latex agglutination slide test intended for qualitative and semi-quantitative in vitro diagnostic determination of C-Reactive Protein (CRP) concentration in serum. CRP - CP2714
	The device is intended for the quantitative in vitro diagnostic determination of C-Reactive Protein (CRP) concentration in serum. CRP - CP2572
	The device is intended for the quantitative in vitro diagnostic determination of C-Reactive Protein (CRP) concentration in serum. CRP - CP7949
	The XCRP method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of CRP in serum. CRP - CP2852
	The device is intended for in vitro diagnostic use in the calibration of CRP assays on clinical chemistry systems. CRP CAL - CP2179
	The device is intended for in vitro diagnostic use in the calibration of CRP assays on clinical chemistry systems. CRP CAL - CP2479
	The device is intended for in vitro diagnostic use in the calibration of CRP assays on clinical chemistry systems. CRP CAL - CP2499
	This product is intended for in vitro diagnostic use, in the quality control of diagnostic methods using CSF as a sample on clinical chemistry systems. The CSF controls are for the control of accuracy. CSF CONTROL - LEVEL 2 (CSF CONTROL 2) - CF1500
	This product is intended for in vitro diagnostic use, in the quality control of diagnostic methods using CSF as a sample on clinical chemistry systems. The CSF controls are for the control of accuracy. CSF CONTROL - LEVEL 3 (CSF CONTROL 3) - CF1501
	The device is intended for the quantitative in vitro determination of Cystatin C in serum or plasma. CYSC - CYS4004
	The device is intended to be used for in the calibration of Cystatin C assays. CYSC CAL - CYS2699
	Intended for in vitro diagnostic (IVD) use in the calibration of Randox Cystatin C assay. For use in a clinical laboratory setting by trained personnel. CYSTATIN C CALIBRATOR (CYSC CAL) - CYS10445
	Intended for in vitro diagnostic (IVD) use in quality control of Randox Cystatin C assay. For use in a clinical laboratory setting by trained personnel. CYSTATIN C CONTROL - LEVEL 2 (CYSC CONTROL 2) - CYS10446
	The Cystatin C Control is intended for use with in vitro diagnostic assays for the quantitative determination of Cystatin C. Cystatin C Control is assayed with target values and it is suitable for use on automated analysers. CYSTATIN C CONTROL - LEVEL 2 (CYSC CONTROL 2) - CYS5019
	Intended for in vitro diagnostic (IVD) use in quality control of Randox Cystatin C assay. For use in a clinical laboratory setting by trained personnel. CYSTATIN C CONTROL - LEVEL 3 (CYSC CONTROL 3) - CYS10447
	The Cystatin C Control is intended for use with in vitro diagnostic assays for the quantitative determination of Cystatin C. Cystatin C Control is assayed with target values, and it is suitable for use on automated analysers. CYSTATIN C CONTROL - LEVEL 3 (CYSC CONTROL 3) - CYS5020
	"Randox Cytokine controls are intended for use as an assayed quality control in the routine monitoring of accuracy and precision for the analytes listed in this insert.The Randox Cytokine Controls are multi-analyte. Each control contains all of the analytes listed overleaf. There are 3 levels of control: low, medium and high; Level 1, 2 and 3 respectively. " CYTOKINE CONTROLS (CTK CONTROL) - CY5006
	Randox Cytokine high sensitivity controls are intended for use as an assayed quality control in the routine monitoring of accuracy and precision for the analytes listed in this insert. The Randox Cytokine high sensitivity controls are multi-analyte. Each control contains all of the analytes listed overleaf. There are 3 levels of control: low, medium and high; Level 1, 2 and 3 respectively. CYTOKINE HIGH SENSITIVITY CONTROLS (CTK HS CONTROL) - CY5005
	The DBIL method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of direct (conjugated) bilirubin in serum or plasma. D BIL - BR2801
	The device is intended for the quantitative in vitro determination of direct bilirubin in serum or plasma. D BIL - BR2362
	The device is intended for the quantitative in vitro determination of direct bilirubin in serum or plasma. D BIL - BR3807
	The device is intended for the quantitative in vitro determination of direct bilirubin in serum or plasma. D BIL - BR8308
	The device is intended for the quantitative in vitro determination of direct bilirubin in serum or plasma. D BIL - BR9765
	The device is intended for in vitro diagnostic use in the calibration of Randox HDL and LDL cholesterol clearance methods D LDL/HDL CAL - CH2673
	D-3 Hydroxybutyrate (RANBUT) D-3 Hydroxybutyrate (RANBUT) - RB1007
	D-3 Hydroxybutyrate (RANBUT) D-3 Hydroxybutyrate (RANBUT) - RB1008
	For the quantitative in vitro determination of Digoxin in human serum DG - TD3410
	The Direct Bilirubin test system is a device intended for the quantitative in vitro determination of Direct Bilirubin in serum and plasma. DIRECT BILIRUBIN 2 (D BIL 2) - BR8376
	DIRECT HDL-CHOLESTEROL (HDL) DIRECT HDL-CHOLESTEROL (HDL) - CH8033
	Enzymatic Clearance assay for the in vitro quantitative determination of HDL-cholesterol in human serum and plasma. DIRECT HDL-CHOLESTEROL (HDL) - CH1383
	Enzymatic Clearance assay for the in vitro quantitative determination of HDL-cholesterol in human serum and plasma. DIRECT HDL-CHOLESTEROL (HDL) - CH2655
	For the quantitative in vitro determination of HDL Cholesterol in serum and plasma. DIRECT HDL-CHOLESTEROL (HDL) - CH8311
	DIRECT LDL-CHOLESTEROL (LDL) DIRECT LDL-CHOLESTEROL (LDL) - CH8032
	DIRECT LDL-CHOLESTEROL (LDL) DIRECT LDL-CHOLESTEROL (LDL) - CH8312
	Enzymatic Clearance assay for the in vitro quantitative determination of LDL-cholesterol in human serum and plasma. DIRECT LDL-CHOLESTEROL (LDL) - CH2656
	Diluted displacement fluid is used to wash the Evidence™ reagent tubing between dispenses. DISP FL (conc.) - EV3580
	The Evidence® Drugs of Abuse (DOA) Assays are in-vitro diagnostic tests for the qualitative determination of the parent molecule and metabolites of drugs in human urine. They are competitive enzyme immunoassays. DOA - EV3500
	The Evidence® Drugs of Abuse (DOA) Assays are in-vitro diagnostic tests for the qualitative determination of the parent molecule and metabolites of drugs in human urine. They are competitive enzyme immunoassays. DOA - EV3542
	Evidence® Drugs of Abuse Calibrators are intended for in vitro diagnostic use in the calibration of the Randox Drugs of Abuse Panel on the Evidence® analyser. DOA CAL - EV3550
	The Randox Multidrug Calibrator Set is intended for use in the calibration of Methamphetamine, Barbiturates, Cocaine Metabolite, Methadone and Opiate assays. DOA CAL - DA2704
	The Randox Multidrug Control Level 1 is intended for use in the Quality Control of Methamphetamine, Barbiturates, Cocaine, Methadone and Opiates assays. DOA CONTROL 1 - DA3121
	The Randox Multidrug Control Level 2 is intended for use in the Quality Control of Methamphetamine, Barbiturates, Cocaine, Methadone and Opiates assays. DOA CONTROL 2 - DA3122
	This product is intended for in vitro diagnostic use in the quality control of drug residue analysis on clinical chemistry systems. TheDrug Controls are for the control of accuracy and precision. DRUG CONTROL - LEVEL 1 (TDM CONTROL 1) - HD1667
	This product is intended for in vitro diagnostic use in the quality control of drug residue analysis on clinical chemistry systems. The Drug Controls are for the control of accuracy and precision. DRUG CONTROL - LEVEL 2 (TDM CONTROL 2) - HD1668
	This product is intended for in vitro diagnostic use in the quality control of drug residue analysis on clinical chemistry systems. The Drug Controls are for the control of accuracy and precision. DRUG CONTROL - LEVEL 3 (TDM CONTROL 3) - HD1669
	The EDDP assay is an in vitro diagnostic test for the qualitative and semi-quantitative detection of 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) in human urine. EDDP - DA4013
	The Randox EDDP Calibrator Set is intended for use in the calibration of the 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) assay. EDDP CAL - DA2702
	The Randox EDDP Control - Level 1 is intended for use in the Quality Control of the 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) assay. The EDDP Control - Level 1 contains the specific drug EDDP. EDDP CONTROL 1 - DA3123
	The Randox EDDP Control - Level 2 is intended for use in the Quality Control of the 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP) assay. The EDDP Control - Level 2 contains the specific drug EDDP. EDDP CONTROL 2 - DA3124
	Enzymes Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of Roche Systems for ALT, AST, Alkaline Phosphatase (ALP), Total Amylase, Pancreatic Amylase, CK, CKMB, Gamma GT, LDH and Lipase assays. ENZYMES LINEARITY VERIFIER (For Roche Systems) (ENZYMES LIN VER ROCHE) - LV10366
	Esoteric Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of the Roche Systems for Acetaminophen, Ammonia, Ethanol, Salicylate, Microalbumin and Urinary Protein assays. ESOTERIC LINEARITY VERIFIERS (For Roche Systems) (ESOTERIC LIN VER ROCHE) - LV10336
	The Blood Sample Collection Kit is intended for use in the collection and transport of a blood sample, taken by a trained phlebotomist. The samples will be transported to a professional laboratory for testing. ESSENTIAL PACKAGE SAMPLE COLLECTION KIT (USA) - SCK10684
	This should be run on a weekly basis to prevent protein build up. ETCH - RX4048
	The ethanol assay is an in vitro diagnostic test for the quantitative analysis of ethanol in human urine and serum. EtOH - DA4015
	The Randox Ethanol Calibrator and Control Set is intended for the calibration and quality control of the Randox Ethanol assay, which is used for the quantitative analysis of ethanol in human urine and serum. EtOH CAL/CONTROL - DA2703
	The Evidence MultiSTAT is a benchtop, fully automated, immunoassay analyser that has been designed and developed to be operated in a wide range of laboratory settings within different industries. These include clinical, hospital, academic, research and development, veterinary and food laboratories. Evidence MultiSTAT - EV4115
	The Evidence MultiSTAT DOA Urine MultiPlex is intended for use with the Evidence MultiSTAT. The Evidence MultiSTAT is an analyzer intended for the qualitative determination of parent drug molecule and metabolites of drugs in human urine at the associated cut offs. Evidence MultiSTAT DOA Urine MultiPlex - EV4393
	The Blood Sample Collection Kit is intended for use in the collection and transport of a blood sample, taken by a trained phlebotomist. The samples will be transported to a professional laboratory for testing. EXTENDED PACKAGE SAMPLE COLLECTION KIT (USA U60) - SCK10689
	The Blood Sample Collection Kit is intended for use in the collection and transport of a blood sample, taken by a trained phlebotomist. The samples will be transported to a professional laboratory for testing. EXTENDED PACKAGE SAMPLE COLLECTION KIT (USA) - SCK10685
	The product is an in vitro diagnostic test intended for the quantitative determination of Iron in serum Fe - SI2818
	The product is intended for the quantitative in vitro determination of Iron in serum and plasma Fe - SI3821
	The product is intended for the quantitative in vitro determination of Iron in serum and plasma Fe - SI7967
	This product is intended for the quantitative in vitro determination of Iron in serum. Fe - SI257
	This product is intended for the quantitative in vitro determination of Ferritin in serum or plasma. FERR - FN3452
	This product is intended for the quantitative in vitro determination of Ferritin in serum or plasma. FERR - FN3453
	This product is intended for the quantitative in vitro determination of Ferritin in serum or plasma. FERR - FN3888
	The CRP test system is intended for the quantitative in vitro determination of C-Reactive Protein (CRP) concentration in serum or plasma. frCRP - CP3847
	The CRP test system is intended for the quantitative in vitro determination of C-Reactive Protein (CRP) concentration in serum or plasma. frCRP - CP3849
	The CRP test system is intended for the quantitative in vitro determination of C-Reactive Protein (CRP) concentration in serum or plasma. frCRP - CP3850
	Enzymatic assay for the quantitative in vitro determination of glycated protein (fructosamine) in human serum or plasma. FRUC - FR3133
	This product is intended for in vitro diagnostic use in the calibration of the Randox Liquid Fructosamine assay on clinical chemistry systems. FRUC CAL - FR2993
	This product is intended for in vitro diagnostic use in the quality control of the Randox Liquid Fructosamine assay on clinical chemistry systems. FRUC CONTROL 1 - FR2994
	This product is intended for in vitro diagnostic use in the quality control of the Randox Liquid Fructosamine assay on clinical chemistry systems. FRUC CONTROL 3 - FR2996
	FRUCTOSAMINE (FRUC) FRUCTOSAMINE (FRUC) - FR4030
	G-6-PDH DEFICIENT CONTROL (G-6-PDH CONTROL D) G-6-PDH DEFICIENT CONTROL (G-6-PDH CONTROL D) - PD2617
	G-6-PDH NORMAL CONTROL (G-6-PDH CONTROL N) G-6-PDH NORMAL CONTROL (G-6-PDH CONTROL N) - PD2618
	A Gamma GT test system is a device intended for the quantitative in vitro determination of L Gamma Glutamyltransferase (GGT) activity in serum and plasma. GAMMA-GLUTAMYLTRANSERASE (GGT) - GT3874
	A Gamma GT test system is a device intended for the quantitative in vitro determination of L Gamma Glutamyltransferase (GGT) activity in serum and plasma. GAMMA-GLUTAMYLTRANSERASE (GGT) - GT8146
	A Gamma GT test system is a device intended for the quantitative in vitro determination of L Gamma Glutamyltransferase (GGT) activity in serum. GAMMA-GLUTAMYLTRANSERASE (GGT) - GT8320
	For the quantitative in vitro determination of Gentamicin in human serum GENT - TD3413
	A GGT test system is a device intended for the quantitative in vitro determination of L Gamma Glutamyltransferase (GGT) activity in serum and plasma. This product is suitable for use on RX series instruments which includes the RX daytona and the RX imola. GGT - GT3817
	A Glucose test system is a device intended for the quantitative in vitro determination of glucose concentration in serum, lithium plasma and urine GLUC-HK - GL3816
	A Glucose test system is a device intended for the quantitative in vitro determination of glucose concentration in serum, lithium plasma and urine GLUC-HK - GL3881
	A Glucose test system is a device intended for the quantitative in vitro determination of glucose concentration in serum, plasma and urine GLUC-HK - GL1611
	A Glucose test system is a device intended for the quantitative in vitro determination of glucose concentration in serum, plasma and urine GLUC-HK - GL2822
	The product is intended for the quantitative in vitro determination of Glucose in serum or urine. GLUC-HK - GL8319
	The product is intended for the quantitative in vitro determination of Glucose in serum, plasma or urine. GLUC-HK - GL7954
	A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine GLUC-PAP - GL1021
	A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine GLUC-PAP - GL2614
	A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine GLUC-PAP - GL2623
	A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine GLUC-PAP - GL364
	A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine GLUC-PAP - GL366
	A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine GLUC-PAP - GL3815
	A glucose test system is a device intended for the quantitative in vitro determination of Glucose concentration in serum, plasma and urine GLUC-PAP - GL3981
	The product is intended for the quantitative in vitro determination of Glucose in serum, plasma or urine. GLUC-PAP - GL7952
	GLUTATHIONE REDUCTASE (GLUT RED) GLUTATHIONE REDUCTASE (GLUT RED) - GR2368
	GLUTATHIONE REDUCTASE CALIBRATION SERUM (GLUT RED CAL) GLUTATHIONE REDUCTASE CALIBRATION SERUM (GLUT RED CAL) - GR2609
	GLUTATHIONE REDUCTASE CONTROL SERUM (GLUT RED CONTROL) GLUTATHIONE REDUCTASE CONTROL SERUM (GLUT RED CONTROL) - GR2608
	GLYCEROL (GLY) GLYCEROL (GLY) - GY105
	GLYCEROL CONTROL (GLY CONTROL) GLYCEROL CONTROL (GLY CONTROL) - GY1369
	Used as a Calibrator in a two-point calibration. H Solution is aspirated from a sample cup located in a pre-registered position on the sample carousel. H SOLN - RX4046
	This product is intended for in vitro diagnostic use in the quality control of multiple haematology parameters HAEM CNTL - LEVEL 1, 2, 3 - HM5162
	HAEMATOLOGY CONTROL - LEVEL 1 (HAEM CNTL - LEVEL 1) HAEMATOLOGY CONTROL - LEVEL 1 (HAEM CNTL - LEVEL 1) - HM10190
	HAEMATOLOGY CONTROL - LEVEL 2 (HAEM CNTL - LEVEL 2) HAEMATOLOGY CONTROL - LEVEL 2 (HAEM CNTL - LEVEL 2) - HM10191
	HAEMATOLOGY CONTROL - LEVEL 3 (HAEM CNTL - LEVEL 3) HAEMATOLOGY CONTROL - LEVEL 3 (HAEM CNTL - LEVEL 3) - HM10192
	HAEMOGLOBIN A1c (HbA1c) HAEMOGLOBIN A1c (HbA1c) - HA3450
	HAEMOGLOBIN F AND A2 CONTROLS - LEVEL 1 AND 2 (Hb F & A2 CONTROL) HAEMOGLOBIN F AND A2 CONTROLS - LEVEL 1 AND 2 (Hb F & A2 CONTROL) - HA5083
	HAPTOGLOBIN (HP) HAPTOGLOBIN (HP) - HP3886
	A Haemoglobin A1c test system is a device intended for the quantitative in vitro determination of Haemoglobin A1c concentration in whole blood HbA1C - HA3830
	The product is intended for the quantitative in vitro determination of Haemoglobin A1c concentration in whole blood. HbA1C - HA8321
	This product is intended for in vitro diagnostic use in the calibration of HbA1c on clinical chemistry systems. HbA1C CAL - HA3444
	This product is intended for in vitro diagnostic use in the quality control of HbA1c on clinical chemistry systems. HbA1C CONTROL - HA5072
	The HbA1c II Calibrator is intended for use in the calibration of the HbA1c II assay. HbA1c II CALIBRATOR SET (HbA1c II CAL) - HA8124
	A homocysteine test system is a device intended for the quantitative in vitro determination of homocysteine concentration in human serum. HCY - HY4036
	An HDL-cholesterol test system is a device intended for the quantitative in vitro determination of HDL-cholesterol concentration in human serum and plasma. HDL - CH3811
	HDL-CHOLESTEROL (HDL) HDL-CHOLESTEROL (HDL) - CH203
	High Sensitivity C-Reactive Protein Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of Roche systems for High Sensitivity C-reactive protein (hsCRP). HIGH SENSITIVITY C-REACTIVE PROTEIN LINEARITY VERIFIERS (For Roche Series) - LV10335
	Randox High Sensitivity CRP Control Level I is a ready to use control in a stabilised protein base. It is intended for use with the Randox High Sensitivity CRP Assay (Catalogue No. CP3885) for the control of accuracy and the control of reproducibility. HIGH SENSITIVITY CRP CONTROL - LEVEL I (hsCRP CONTROL 1) - CP2476
	Randox High Sensitivity CRP Control Level II is a ready to use control in a stabilised protein base. It is intended for use with the Randox High Sensitivity CRP Assay (Catalogue No. CP3885) for the control of accuracy and the control of reproducibility. HIGH SENSITIVITY CRP CONTROL - LEVEL II (hsCRP CONTROL 2) - CP2477
	The CRP test system is intended for the quantitative in vitro determination of C-Reactive Protein (CRP) concentration in serum or plasma. hsCRP - CP3885
	The device is intended for in vitro diagnostic use in the calibration of CRP assays on clinical chemistry systems. hsCRP CAL - CP2478
	The Human Assayed Multi-sera is supplied at 2 levels, level 2 and 3. Target values and ranges are supplied for the analytes listed in the values section at both levels. HUMAN ASSAYED MULTI-SERA/ASSAYED CHEMISTRY PREMIUM PLUS - LEVEL 2 & 3 (HUM ASY - HS2611
	The Human Assayed Multi-sera is supplied at 2 levels, level 2 and 3. Target values and ranges are supplied for the analytes listed in the values section at both levels. HUMAN ASSAYED MULTI-SERA/ASSAYED CHEMISTRY PREMIUM PLUS - LEVEL 2 (HUM ASY CONTR - HN1530
	The Human Assayed Multi-sera is supplied at 2 levels, level 2 and 3. Target values and ranges are supplied for the analytes listed in the values section at both levels. HUMAN ASSAYED MULTI-SERA/ASSAYED CHEMISTRY PREMIUM PLUS - LEVEL 3 (HUM ASY CONTR - HE1532
	HUMAN PRECISION CONTROL - LEVEL 2 (HUM PREC CONTROL 2) HUMAN PRECISION CONTROL - LEVEL 2 (HUM PREC CONTROL 2) - UN1557
	HUMAN PRECISION CONTROL - LEVEL 3 (HUM PREC CONTROL 3) HUMAN PRECISION CONTROL - LEVEL 3 (HUM PREC CONTROL 3) - UE1558
	Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine. I.S.E. CL - D200-0016
	Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine. I.S.E. CL - D400-0013
	The product should be run on a weekly basis to prevent protein build up. I.S.E. CLN - RX4047
	Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine. I.S.E. K - D200-0015
	Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine. I.S.E. K - D400-0012
	Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine. I.S.E. NA - D200-0014
	Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine. I.S.E. NA - D400-0011
	Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine. I.S.E. REF - D200-0017
	Intended for use with the Ion Selective Electrode unit for measuring concentration of electrolytes in the blood serum, plasma or urine. I.S.E. REF - D400-0010
	The product is intended for the quantitative in vitro determination of IgA in serum or plasma. IgA - IA2447
	The product is intended for the quantitative in vitro determination of IgA in serum or plasma. IgA - IA3832
	The product is intended for the quantitative in vitro determination of IgA in serum or plasma. IgA - IA3895
	The product is intended for the quantitative in vitro determination of IgA in serum or plasma. IgA - IA7157
	An IgE test system is a device intended for the quantitative in vitro determination of immunoglobulin E (IgE) concentration in human serum or plasma IgE - IE7308
	This product is intended for in vitro diagnostic use in the quality control of IgE on clinical chemistry systems. IgE CAL SET - IE2492
	IgG IgG - IG3896
	The IgG test system is a device intended for the quantitative in vitro determination of immunoglobulin G (IgG) concentration in serum and plasma IgG - IG2448
	The IgG test system is a device intended for the quantitative in vitro determination of immunoglobulin G (IgG) concentration in serum and plasma IgG - IG3833
	The IgG test system is a device intended for the quantitative in vitro determination of immunoglobulin G (IgG) concentration in serum and plasma IgG - IG7158
	For the quantitative in vitro determination of IgM in serum and plasma IgM - IM3834
	For the quantitative in vitro determination of IgM in serum and plasma IgM - IM7977
	This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes listed in the package insert. IMMUNOASSAY PREMIUM - LEVEL 1 (IA PREMIUM 1) - IA2638
	This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes listed in the package insert. IMMUNOASSAY PREMIUM - LEVEL 2 (IA PREMIUM 2) - IA2639
	This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes listed in the package insert. IMMUNOASSAY PREMIUM - LEVEL 3 (IA PREMIUM 3) - IA2640
	This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility ofanalytes listed in the package insert. IMMUNOASSAY PREMIUM - TRI-LEVEL (IA PREMIUM 1, 2 AND 3) - IA2633
	This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility ofanalytes listed in the package insert. IMMUNOASSAY PREMIUM PLUS - LEVEL 1 (IA PREMIUM PLUS 1) - IA3109
	This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes listed in the package insert. IMMUNOASSAY PREMIUM PLUS - LEVEL 2 (IA PREMIUM PLUS 2) - IA3110
	This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes listed in the package insert. IMMUNOASSAY PREMIUM PLUS - LEVEL 3 (IA PREMIUM PLUS 3) - IA3111
	This product is intended for in vitro diagnostic use, as assayed quality control material to monitor the accuracy and reproducibility of analytes listed in the package insert. IMMUNOASSAY PREMIUM PLUS - TRI-LEVEL (IA PREMIUM PLUS 1, 2 AND 3) - IA3112
	This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Immunoassays on clinical chemistry systems. This material can be used to monitor the control of accuracy or the control of reproducibility of immunoassays. IMMUNOASSAY SPECIALITY I - LEVEL 1 (IA SPECIALITY I LEV 1) - IAS3113
	This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Immunoassays on clinical chemistry systems. This material can be used to monitor the control of accuracy or the control of reproducibility of immunoassays. IMMUNOASSAY SPECIALITY I - LEVEL 2 (IA SPECIALITY I LEV 2) - IAS3114
	This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Immunoassays on clinical chemistry systems. This material can be used to monitor the control of accuracy or the control of reproducibility of immunoassays. IMMUNOASSAY SPECIALITY I - LEVEL 3 (IA SPECIALITY I LEV 3) - IAS3115
	This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Immunoassays on clinical chemistry systems. Thismaterial can be used to monitor the control of accuracy or the control of reproducibility of immunoassays. IMMUNOASSAY SPECIALITY II - LEVEL 1 (IA SPECIALITY II LEV 1) - IAS3117
	This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Immunoassays on clinical chemistry systems. Thismaterial can be used to monitor the control of accuracy or the control of reproducibility of immunoassays. IMMUNOASSAY SPECIALITY II - LEVEL 2 (IA SPECIALITY II LEV 2) - IAS3118
	This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Immunoassays on clinical chemistry systems. Thismaterial can be used to monitor the control of accuracy or the control of reproducibility of immunoassays. IMMUNOASSAY SPECIALITY II - LEVEL 3 (IA SPECIALITY II LEV 3) - IAS3119
	IMMUNOGLOBULIN LIQUID PROTEIN CALIBRATOR (IG CAL) IMMUNOGLOBULIN LIQUID PROTEIN CALIBRATOR (IG CAL) - IT3861
	INORGANIC PHOSPHOROUS (PHOS) INORGANIC PHOSPHOROUS (PHOS) - PH8048
	INORGANIC PHOSPHOROUS (PHOS) INORGANIC PHOSPHOROUS (PHOS) - PH8328
	An inorganic phosphorous test system is a device intended for the quantitative in vitro determination of inorganic phosphorous concentration in serum and urine. INORGANIC PHOSPHOROUS (PHOS) - PH3872
	IRON (Fe) IRON (Fe) - SI8049
	IRON (Fe) IRON (Fe) - SI8330
	The product is intended for use in the measurement of urine samples. ISE DIL - RX4049
	The product is required for urine samples. Urine samples must be diluted by a factor of 10 to perform urine measurement. The host analyser will mix the diluent and sample before dispensing the diluted sample into the ISE module. ISE DIL URN - RX3950
	Used as a Calibrator in a two-point calibration. L Solution is pumped into the sample port by the L Solution pump and then positioned in front of the sensor. L SOLN - D400-0018
	Used as a Calibrator in a two-point calibration. L Solution is pumped into the sample port by the L Solution pump and then positioned in front of the sensor. L SOLN - RX4044
	The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma. LCO2-2 - CD4006
	The device is intended for the quantitative in vitro determination of carbon dioxide in serum or plasma. LCO2-2 - CD8357
	LD opt. (LDH L-P) LD opt. (LDH L-P) - LD8052
	LD opt. (LDH L-P) LD opt. (LDH L-P) - LD8323
	LD opt. (LDH P-L) LD opt. (LDH P-L) - LD8051
	LD opt. (LDH P-L) LD opt. (LDH P-L) - LD8322
	The LDH method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of lactate dehydrogenase activity in serum or plasma. LDH - LD2812
	A lactate dehydrogenase test system is a device intended for the quantitative in vitro determination of Lactate Dehydrogenase (LD) activity in serum or plasma. LDH L-P - LD7963
	A lactate dehydrogenase test system is a device intended for the quantitative in vitro determination of Lactate Dehydrogenase (LD) activity in serum. LDH L-P - LD3842
	A lactate dehydrogenase test system is a device intended for the quantitative in vitro determination of Lactate Dehydrogenase (LD) activity in serum or plasma. LDH P-L - LD3818
	A lactate dehydrogenase test system is a device intended for the quantitative in vitro determination of Lactate Dehydrogenase (LD) activity in serum or plasma. LDH P-L - LD401
	In Vitro device for the quantitative determination of LDL-Cholesterol in serum and plasma. LDL - CH3841
	LEUCINE ARYLAMIDASE (LAP) LEUCINE ARYLAMIDASE (LAP) - LA561
	The product is intended for the quantitative in vitro determination of Lithium in serum. Li 2 - LM4005
	LIPASE (LPS) LIPASE (LPS) - LI8050
	LIPASE (LPS) LIPASE (LPS) - LI8361
	A Lipase test system is a device intended for the quantitative in vitro determination of Lipase in human serum and plasma LIPASE (LPS) - LI3837
	For the quantitative in vitro determination of Lipase in human serum and plasma. LIPASE (LPS) - LI7979
	This product is intended for in vitro use in the quality control of Direct HDL, Direct LDL, Lipoprotein (a), ApolipoproteinA-1, Apolipoprotein B, Cholesterol and Triglyceride methods on clinical chemistry systems. LIPID CONTROL - LEVEL 1 (LPD CONTROL 1) - LE2661
	This product is intended for in vitro use in the quality control of Direct HDL, Direct LDL, Lipoprotein (a), ApolipoproteinA-1, Apolipoprotein B, Cholesterol and Triglyceride methods on clinical chemistry systems. LIPID CONTROL - LEVEL 1 (LPD CONTROL 1) - LE2668
	This product is intended for in vitro use in the quality control of Direct HDL, Direct LDL, Lipoprotein (a), ApolipoproteinA-1, Apolipoprotein B, Cholesterol and Triglyceride methods on clinical chemistry systems. LIPID CONTROL - LEVEL 2 (LPD CONTROL 2) - LE2662
	This product is intended for in vitro use in the quality control of Direct HDL, Direct LDL, Lipoprotein (a), ApolipoproteinA-1, Apolipoprotein B, Cholesterol and Triglyceride methods on clinical chemistry systems. LIPID CONTROL - LEVEL 2 (LPD CONTROL 2) - LE2669
	This product is intended for in vitro use in the quality control of Direct HDL, Direct LDL, Lipoprotein (a), ApolipoproteinA-1, Apolipoprotein B, Cholesterol and Triglyceride methods on clinical chemistry systems. LIPID CONTROL - LEVEL 3 (LPD CONTROL 3) - LE2663
	This product is intended for in vitro use in the quality control of Direct HDL, Direct LDL, Lipoprotein (a), ApolipoproteinA-1, Apolipoprotein B, Cholesterol and Triglyceride methods on clinical chemistry systems. LIPID CONTROL - LEVEL 3 (LPD CONTROL 3) - LE2670
	Lipid Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of Beckman Coulter AU Systems for HDL, LDL and Triglycerides. LIPID LINEARITY VERIFIERS (For Beckman Coulter AU Systems) (Lipid LinVer - BC) - LV10364
	Lipid Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of Roche Systems for Cholesterol, HDL, LDL and Triglycerides. LIPID LINEARITY VERIFIERS (For Roche Systems) (LLV-R) - LV10344
	LIPOPROTEIN (a) (Lp (a)) LIPOPROTEIN (a) (Lp (a)) - LP8054
	LIPOPROTEIN (a) (Lp (a)) LIPOPROTEIN (a) (Lp (a)) - LP8324
	Randox Lipoprotein(a) level 3 control is based on lyophilised human serum containing Lipoprotein(a). LIPOPROTEIN (a) CONTROL (Lp (a) CONTROL 3) - LP3406
	LIQUID ASSAYED CHEMISTRY CONTROL PREMIUM – LEVEL 2 (LIQ CHEM ASY PREMIUM 2) LIQUID ASSAYED CHEMISTRY CONTROL PREMIUM – LEVEL 2 (LIQ CHEM ASY PREMIUM 2) - LAN4216
	LIQUID ASSAYED CHEMISTRY CONTROL PREMIUM – LEVEL 3 (LIQ CHEM ASY PREMIUM 3) LIQUID ASSAYED CHEMISTRY CONTROL PREMIUM – LEVEL 3 (LIQ CHEM ASY PREMIUM 3) - LAE4217
	This product is intended for in vitro diagnostic use, in the quality control of diagnostic assays. The Liquid Assayed Chemistry Control Premium Plus is for the control of accuracy. LIQUID ASSAYED CHEMISTRY CONTROL PREMIUM PLUS - LEVEL 1 (LIQ CHEM ASY PREMIUM PL - LAL4213
	This product is intended for in vitro diagnostic use, in the quality control of diagnostic assays. The Liquid Assayed Chemistry Control Premium Plus is for the control of accuracy. LIQUID ASSAYED CHEMISTRY CONTROL PREMIUM PLUS - LEVEL 2 (LIQ CHEM ASY PREMIUM PL - LAN4214
	This product is intended for in vitro diagnostic use, in the quality control of diagnostic assays. The Liquid Assayed Chemistry Control Premium Plus is for the control of accuracy. LIQUID ASSAYED CHEMISTRY CONTROL PREMIUM PLUS - LEVEL 3 (LIQ CHEM ASY PREMIUM PL - LAE4215
	LIQUID BILIRUBIN CONTROL - LEVEL 1 (LIQ BIL CONTROL 1) LIQUID BILIRUBIN CONTROL - LEVEL 1 (LIQ BIL CONTROL 1) - BR10172
	LIQUID BILIRUBIN CONTROL - LEVEL 2 (LIQ BIL CONTROL 2) LIQUID BILIRUBIN CONTROL - LEVEL 2 (LIQ BIL CONTROL 2) - BR10173
	LIQUID CHEMISTRY PREMIUM - LEVEL 2 (LIQ CHEM PREMIUM 2) LIQUID CHEMISTRY PREMIUM - LEVEL 2 (LIQ CHEM PREMIUM 2) - LUN5048
	LIQUID CHEMISTRY PREMIUM - LEVEL 3 (LIQ CHEM PREMIUM 3) LIQUID CHEMISTRY PREMIUM - LEVEL 3 (LIQ CHEM PREMIUM 3) - LUE5049
	LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 1 (LIQ CHEM PREMIUM PLUS 1) LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 1 (LIQ CHEM PREMIUM PLUS 1) - LUL5069
	LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 1 (LIQ CHEM PREMIUM PLUS 1) LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 1 (LIQ CHEM PREMIUM PLUS 1) - LUL5093
	LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 2 (LIQ CHEM PREMIUM PLUS 2) LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 2 (LIQ CHEM PREMIUM PLUS 2) - LUN5070
	LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 2 (LIQ CHEM PREMIUM PLUS 2) LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 2 (LIQ CHEM PREMIUM PLUS 2) - LUN5094
	LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 3 (LIQ CHEM PREMIUM PLUS 3) LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 3 (LIQ CHEM PREMIUM PLUS 3) - LUE5071
	LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 3 (LIQ CHEM PREMIUM PLUS 3) LIQUID CHEMISTRY PREMIUM PLUS - LEVEL 3 (LIQ CHEM PREMIUM PLUS 3) - LUE5095
	This product is intended for in vitro diagnostic use in the quality control of CRP on clinical chemistry systems. LIQUID CRP CONTROL - LEVEL 2 (CRP CONTROL 2) - CP2480
	This product is intended for in vitro diagnostic use, in the quality control of CRP on clinical chemistry systems. LIQUID CRP CONTROL - LEVEL 3 (CRP CONTROL 3) - CP2481
	LIQUID CSF CONTROL - LEVEL 1 (CSF CONTROL 1) LIQUID CSF CONTROL - LEVEL 1 (CSF CONTROL 1) - CF10138
	LIQUID CSF CONTROL - LEVEL 2 (CSF CONTROL 2) LIQUID CSF CONTROL - LEVEL 2 (CSF CONTROL 2) - CF10139
	Intended for in vitro diagnostic (IVD) use as a quality control material for determination of Total Bilirubin and Direct Bilirubin on chemistry analysers. For use in a clinical laboratory setting by trained personnel. LIQUID FROZEN BILIRUBIN CONTROL - LEVEL 1 (LIQ BIL CONTROL 1) - BR10442
	Intended for in vitro diagnostic (IVD) use as a quality control material for determination of Total Bilirubin and Direct Bilirubin on chemistry analysers. For use in a clinical laboratory setting by trained personnel. LIQUID FROZEN BILIRUBIN CONTROL - LEVEL 2 (LIQ BIL CONTROL 2) - BR10443
	LIQUID FROZEN LIPID CONTROL - LEVEL 1 (LIQ LPD CONTROL 1) LIQUID FROZEN LIPID CONTROL - LEVEL 1 (LIQ LPD CONTROL 1) - LE10174
	LIQUID FROZEN LIPID CONTROL - LEVEL 2 (LIQ LPD CONTROL 2) LIQUID FROZEN LIPID CONTROL - LEVEL 2 (LIQ LPD CONTROL 2) - LE10175
	LIQUID FROZEN LIPID CONTROL - LEVEL 3 (LIQ LPD CONTROL 3) LIQUID FROZEN LIPID CONTROL - LEVEL 3 (LIQ LPD CONTROL 3) - LE10176
	This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Glycated Haemoglobin (HbA1c) on clinical chemistry systems. Liquid Glycated Haemoglobin (HbA1c) Control Level 1 (LIQ HbA1c CONTROL LEVEL 1) - HA10224
	This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Glycated Haemoglobin (HbA1c) on clinical chemistry systems. Liquid Glycated Haemoglobin (HbA1c) Control Level 2 (LIQ HbA1c CONTROL LEVEL 2) - HA10225
	This product is intended for in vitro diagnostic use, in the quality control of the accuracy of Glycated Haemoglobin (HbA1c) on clinical chemistry systems. Liquid Glycated Haemoglobin (HbA1c) Control set (LIQ HbA1c CONTROL) - HA10155
	The Randox Liquid Immunoassay Premium - Tri-Level are liquid controls developed for use in the quality control of quantitative assays statedin this package insert. LIQUID IMMUNOASSAY PREMIUM - TRI-LEVEL (LIQ IA PREMIUM 1, 2 AND 3) - LIA3108
	For the quantitative in vitro determination of D-3-Hydroxybutyrate in serum and plasma. LIQUID RANBUT (RBT) - RB4067
	For the quantitative in vitro determination of D-3-Hydroxybutyrate in serum and plasma. LIQUID RANBUT (RBT) - RB8378
	The Randox Liquid Urine Control Level 2 is intended for in vitro diagnostic use, in the quality control of Amylase, Calcium, Chloride,Cortisol, Creatinine, Glucose, hCG pregnancy, Magnesium, Microalbumin, Osmolality, pH, Phosphate Inorganic, Potassium,Protein Total, Sodium, Specific Gravity, Urea and Uric Acid (Urate) on clinical chemistry systems. The Liquid Urine Control is for thecontrol of accuracy. LIQUID URINE CONTROL - LEVEL 2 (LIQ URN CONTROL 2) - UC5074
	The Randox Liquid Urine Control - Level 3 is intended for in vitro diagnostic use, in the quality control of Amylase, Calcium, Chloride,Cortisol, Creatinine, Glucose, hCG pregnancy, Magnesium, Microalbumin, Osmolality, pH, Phosphate Inorganic, Potassium,Protein Total, Sodium, Specific Gravity, Urea and Uric Acid (Urate) on clinical chemistry systems. The Liquid Urine Control is for thecontrol of accuracy. LIQUID URINE CONTROL - LEVEL 3 (LIQ URN CONTROL 3) - UC5075
	L-LACTATE (LAC) L-LACTATE (LAC) - LC2389
	L-LACTATE (LAC) L-LACTATE (LAC) - LC3980
	For the quantitative in vitro determination of Lipoprotein (a) in human serum or plasma. Lp (a) - LP2878
	Immunoturbidimetric assay for the quantitative in vitro determination of Lipoprotein(a) in human serum or plasma. Lp (a) - LP2757
	Immunoturbidimetric assay for the quantitative in vitro determination of Lipoprotein(a) in human serum or plasma. Lp (a) - LP3403
	This product is intended for use in the calibration of Lipoprotein(a) assays. Lp(a) CAL SET - LP3404
	MAGNESIUM (Mg) MAGNESIUM (Mg) - MG3880
	MAGNESIUM (Mg) MAGNESIUM (Mg) - MG8326
	A Microalbumin test system is a device intended for the quantitative in vitro determination of Microalbumin concentration in human urine mALB - MA2864
	A Microalbumin test system is a device intended for the quantitative in vitro determination of Microalbumin concentration in urine mALB - MA3828
	A Microalbumin test system is a device intended for the quantitative in vitro determination of Microalbumin concentration in urine mALB - MA8325
	The product is intended to be used for the quantitative in vitro determination of Microalbumin in urine. mALB - MA2423
	The product is intended to be used for the quantitative in vitro determination of Microalbumin in urine. mALB - MA2426
	This product is intended for in vitro use, in the quality control of Alpha-fetoprotein, Free Beta hCG, Free Estriol, Human Chorionic Gonadotropin, Inhibin A and PAPP-A methods on clinical chemistry systems. MATERNAL CONTROL - LEVEL 1 (MATERNAL CONTROL 1) - MSS5024
	This product is intended for in vitro use in the quality control of Alpha-fetoprotein, Free Beta HCG, Free Estriol, Human Chorionic Gonadotrophin, Inhibin A and PAPP-A methods on clinical chemistry systems. MATERNAL CONTROL - LEVEL 2 (MATERNAL CONTROL 2) - MSS5025
	This product is intended for in vitro use in the quality control of Alpha-fetoprotein, Free Beta HCG, Free Estriol, Human Chorionic Gonadotrophin, Inhibin A and PAPP-A methods on clinical chemistry systems. MATERNAL CONTROL - LEVEL 3 (MATERNAL CONTROL 3) - MSS5026
	The MDMA assay is an in vitro diagnostic reagent. For the qualitative and semi-quantitative analysis of MDMA in human urine. MDMA - DA4014
	The Randox Ecstasy Calibrator Set is intended for use in the calibration of the Ecstasy assay. MDMA CAL - DA2701
	The Randox Ecstasy Control Level 1 is intended for use in the Quality Control of the Ecstasy assay. The Ecstasy Control Level 1 contains the specific drug MDMA (3,4-methylenedioxymethamphetamine). MDMA CONTROL 1 - DA3125
	The Randox Ecstasy Control Level 2 is intended for use in the Quality Control of the Ecstasy assay. The Ecstasy Control Level 2 contains the specific drug MDMA (3,4-methylenedioxymethamphetamine). MDMA CONTROL 2 - DA3126
	The Methadone assay is an in vitro diagnostic test for the qualitative and semi-quantitative detection of methadone in human urine. MDONE - DA4016
	The Methamphetamine assay is an in vitro diagnostic test for the qualitative and semi-quantitative detection of methamphetamine in human urine. METHAMP - DA4007
	MICROALBUMIN (mALB) MICROALBUMIN (mALB) - MA8056
	MICROALBUMIN CALIBRATOR SERIES (mALB CAL) MICROALBUMIN CALIBRATOR SERIES (mALB CAL) - MA1567
	Immunoturbidimetric assay for the quantitative in vitro determination of Myoglobin in human serum. MYO - MY2127
	This product is intended for use in the calibration of Myoglobin immunoturbidimetric assays. MYO CAL SET - MY2456
	This product is intended for the quantitative in vitro determination of Sodium in serum Na - NA8327
	This product is intended for the quantitative in vitro determination of Sodium in serum and plasma Na - NA3851
	This product is intended for the quantitative in vitro determination of Sodium in serum and plasma Na - NA7167
	For the quantitative in vitro determination of Ammonia in plasma. NH3 - AM3979
	Non-Esterified Fatty Acids (NEFA) Non-Esterified Fatty Acids (NEFA) - FA115
	This product should be used in conjunction with RX daytona plus reagents to dilute samples prior to assay. NS - SA8396
	This product should be used in conjunction with RX series reagents to dilute samples prior to assay NS - SA3854
	The Opiates assay is an in vitro diagnostic test for the qualitative and semi-quantitative detection of Opiates in human urine. OPIAT - DA4012
	A Pancreatic α‑Amylase test system is a device intended for the quantitative in vitro determination of Pancreatic α‑Amylase activity in serum, plasma or urine. P AMY - AY2862
	A Pancreatic α‑Amylase test system is a device intended for the quantitative in vitro determination of Pancreatic α‑Amylase activity in serum, plasma or urine. P AMY - AY3855
	The device is intended for the quantitative in vitro determination of pancreatic α amylase in serum, plasma and urine. P AMY - AY7934
	PARATHYROID HORMONE CONTROL - LEVEL 1 (PTH CONTROL 1) PARATHYROID HORMONE CONTROL - LEVEL 1 (PTH CONTROL 1) - PTH10110
	PARATHYROID HORMONE CONTROL - LEVEL 2 (PTH CONTROL 2) PARATHYROID HORMONE CONTROL - LEVEL 2 (PTH CONTROL 2) - PTH10111
	PARATHYROID HORMONE CONTROL - LEVEL 3 (PTH CONTROL 3) PARATHYROID HORMONE CONTROL - LEVEL 3 (PTH CONTROL 3) - PTH10112
	Intended for the quantitative in vitro determination of Phenobarbital in human serum. PHB - TD3408
	The device is intended for the quantitative in vitro determination of Phenytoin in human serum PHT - TD3409
	The PlaySafe kit is intended for use in the collection of a urine sample for laboratory analysis of nine sexually transmitted infections: (Chlamydia trachomatis, Neisseria gonorrhoeae, Herpes simplex virus I, Herpes simplex virus II, Trichomonas vaginalis, Mycoplasma hominis, Mycoplasma genitalium, Ureaplasma urealyticum & Haemophilus ducreyi (chancroid). This device is intended for sample collection purpose only. Samples may be collected at home through adherence to the Instructions for Use (IFU) document or may be collected under the guidance of a medical professional. PlaySafe™ - SCK10690
	For the quantitative in vitro determination of Potassium in serum or plasma. Potassium (K) - PT3852
	For the quantitative in vitro determination of Potassium in serum or plasma. Potassium (K) - PT7168
	A prealbumin (transthyretin) test system is a device intended for the quantitative in vitro determination of prealbumin (transthyretin) concentration in serum. PREALBUMIN (PreALB) - PA3843
	The Precision Check Solution is used for checking proper functioning of the reagent and sample fluid metering and photometric measuring system. PRECISION CHECK SOLUTION (PREC) - RX8142
	The Pre eclampsia Control Level 1 is intended for use with in vitro diagnostic assays for the quantitative determination of placental growth factor (PlGF) and soluble fms like tyrosine kinase 1 (sFlt 1) in human serum and plasma. The Pre eclampsia Control Level 1 is assayed with target values and are suitable for use on various analysers. The Pre eclampsia Control Level 1 is for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation. PRE-ECLAMPSIA CONTROL LEVEL 1 - PE10527
	The Pre eclampsia Control Level 2 is intended for use with in vitro diagnostic assays for the quantitative determination of placental growth factor (PlGF) and soluble fms like tyrosine kinase 1 (sFlt 1) in human serum and plasma. The Pre eclampsia Control Level 2 is assayed with target values and are suitable for use on various analysers. The Pre eclampsia Control Level 2 is for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation. PRE-ECLAMPSIA CONTROL LEVEL 2 - PE10528
	The Pre eclampsia Control Level 3 is intended for use with in vitro diagnostic assays for the quantitative determination of placental growth factor (PlGF) and soluble fms like tyrosine kinase 1 (sFlt 1) in human serum and plasma. The Pre eclampsia Control Level 3 is assayed with target values and are suitable for use on various analysers. The Pre eclampsia Control Level 3 is for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation. PRE-ECLAMPSIA CONTROL LEVEL 3 - PE10529
	The Reagent Precision Test is used on the RX series clinical chemistry systems for checking proper functioning of the reagent fluid metering and photometric measuring system. RABS - RP3857
	The Reagent Precision Test is used on the RX series clinical chemistry systems for checking proper functioning of the reagent fluid metering and photometric measuring system. RABS - RP8398
	The RANDOX evidence® system is a fully automated, continuous access immunoanalyser using protein biochip array technology. It is intended for the in-vitro qualitative, semi-quantitative or fully quantitative determination of various diagnostic markers. Randox Evidence™ - EV3600
	This product is intended for in vitro diagnostic use, in the calibration of the Randox Ransel assay. RANSEL CALIBRATOR (RANSEL CAL) - SC10154
	This product is intended for in vitro diagnostic use in the control of the Randox Ransel assay. RANSEL CONTROL - SC692
	The Ransod Control is intended for use with in vitro diagnostic assays for the quantitative determination of superoxide dismutase. RANSOD CONTROL - SD126
	This is required for the dilution of heparinized or EDTA whole blood samples for use with the Randox Ransod Reagent. RANSOD DILUENT (RANSOD DIL) - SD124
	Chemiluminescent substrate comprised of 1 bottle of Luminol Reagent - EV701 and 1 bottle of Peroxide Reagent. The analyser uses a 1:1 mixture of the two solutions as a working signal reagent - EV701 to generate a chemiluminescent signal which can be detected by the imaging module of the Evidence™ analyser. REAG SGNL - EV701 - EV3601
	Chemiluminescent substrate comprised of 1 bottle of Luminol Reagent - EV805 and 1 bottle of Peroxide Reagent. The analyser uses a 1:1 mixture of the two solutions as a working signal reagent to generate a chemiluminescent signal which can be detected by the imaging module of the Evidence™ analyser. REAG SGNL - EV805 - EV3529
	This is required for measuring reference electrode potential of an ion selective electrode module. REF SOLN - RX4045
	A RF test system is a device intended for the quantitative in vitro determination of Rheumatoid Factors (RF) concentration in serum. RF - RF3836
	Latex agglutination slide test for the qualitative and semi quantitative in vitro determination of Rheumatoid Factor in serum. RF - RF1436
	The product is a latex agglutination slide test for the qualitative and semi quantitative in vitro determination of Rheumatoid Factor in serum. RF - RF2716
	The product is a latex agglutination slide test for the qualitative and semi quantitative in vitro determination of Rheumatoid Factor in serum. RF - RF7980
	The product is a latex agglutination slide test for the qualitative and semi quantitative in vitro determination of Rheumatoid Factor in serum. RF - RF7981
	This product is intended for us as a latex enhanced immunoturbidimetric test for the quantitative in vitro determination of Rheumatoid Factor in serum. RF - RF2881
	This product is intended for in vitro diagnostic use in the calibration of RF on clinical chemistry analysers. RF CAL - RF2301
	Rheumatoid Factor Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of Roche Systems for Rheumatoid Factor (RF). RHEUMATOID FACTOR LINEARITY VERIFIERS (For Roche Systems) (RFLV) - LV10343
	RX Daytona is an automated clinical chemistry analyser complete with dedicated analyser software. RX daytona - RX3900
	The Randox RX daytona plus with ISE is a fully automated, random access, clinical chemistry analyser completewith dedicated analyser software. RX daytona plus - RX4040
	The Randox RX daytona plus without ISE is a fully automated, random access, clinical chemistry analyser completewith dedicated analyser software. RX daytona plus - RX4041
	Rx Imola is an automated clinical chemistry analyser complete with dedicated analyser software. RX imola - RX4900
	The RX monaco Analyser is a fully automated clinical chemistry analyser that has been designed and developed to be operated in a wide range of laboratory settings within different industries. These include clinical, hospital, academic, research and development, veterinary, food and wine laboratories.The RX monaco can detect a wide range of analytes in various liquid matrices. These include serum, plasma, urine, CSF and supernatants.The RX monaco is designed to be used by qualified laboratory staff, in conjunction with current Randox clinical chemistry reagents, to generate a result. The results that are generated are intended to be interpreted by a trained professional to aid in the diagnosis or interpretation of its application.The RX monaco is supplied with dedicated software that has been designed to assist and guide the operator through the operational processes. The software allows the RX monaco to interface with a host system or computer to assist in the processing, storing, ordering and managing of tests and test results. RX monaco - RX5000
	This product is used for checking proper functioning of the sample fluid metering system as well as the photometric measuring system. SABS - SP3856
	This product is used for checking proper functioning of the sample fluid metering system as well as the photometric measuring system. SABS - SP8399
	For the quantitative in vitro determination of Salicylate in human serum SAL - SAL4024
	"SARS-CoV-2 (Severe acute respiratory syndrome coronavirus) Negative/Non-Reactive ControlSARS-CoV-2 Negative/Non-Reactive Control is intended for use with in vitro assays for determination of Total antibodies to SARS-CoV-2 (Severe acute respiratory syndrome coronavirus).SARS-CoV-2 Negative/Non-Reactive Control is unassayed without target values and is suitable for use on various analysers. SARS-CoV-2 Negative/Non-Reactive Control is useful in determining the precision of testing systems and allows performance monitoring of multiple test systems.SARS-CoV-2 (Severe acute respiratory syndrome coronavirus) Positive/Reactive ControlSARS-CoV-2 Positive/Reactive Control is intended for use with in vitro assays for determination of Total antibodies to SARS-CoV-2 (Severe acute respiratory syndrome coronavirus).SARS-CoV-2 Positive/Reactive Control is unassayed without target values and is suitable for use on various analysers. SARS-CoV-2 Negative/Non-Reactive Control is useful in determining the precision of testing systems and allows performance monitoring of multiple test systems." SARS CoV-2 Controls (SARS-CoV-2) - COV10460
	Serology I Postive Control is intended for use with in vitro assays for determination of antibodies to Human Immunodeficiency Virus Type 1 and 2 (HIV-1/2), antibodies to Human T-Lymphotropic Virus Type 1 and 2 (HTLV-1/2), antibodies to Hepatitis C Virus (HCV), Hepatitis B Surface Antigen (HBsAg), IgG antibodies to Hepatitis B Core Antibodies (HBc) and IgG antibodies to Treponema pallidum. Serology I Positive Control is unassayed without target values and is suitable for use on many analysers. These controls must not be used as a substitute for the mandatory manufacturer’s kit controls provided with the assay.Serology I Positive Control is helpful in determining the precision of testing systems and in identifying sources of variation. SEROLOGY I POSITIVE CONTROL (SEROLOGY I CONTROL +) - SR10352
	Serology II Positive Control is intended for use with in vitro assays for determination of antibodies to Hepatitis B Surface Antigen (Anti HBs), IgG antibodies to Hepatitis B Core Antibodies (Anti HBc), antibodies to Hepatitis A (Anti HAV) and antibodies to Hepatitis B Envelope (Anti HBe). Serology II Positive Control is unassayed without target values and is suitable for use on many analysers. These controls must not be used as a substitute for the mandatory manufacturer’s kit controls provided with the assay.Serology II Positive Control is helpful in determining the precision of testing systems and in identifying sources of variation. SEROLOGY II POSITIVE CONTROL (SEROLOGY II CONTROL +) - SR10353
	Serology III Positive Control is intended for use with in vitro assays for determination of IgM antibodies to Hepatitis B Core Antigen (HBc IgM) and IgM antibodies to Hepatitis A (HAV IgM). Serology III Positive Control is unassayed without target values and is suitable for use on many analysers. These controls must not be used as a substitute for the mandatory manufacturer’s kit controls provided with the assay.Serology III Positive Control is helpful in determining the precision of testing systems and in identifying sources of variation. SEROLOGY III POSITIVE CONTROL (SEROLOGY III CONTROL +) - SR10354
	Lyme Disease Negative Control is intended for use as an unassayed non-reactive quality assurance reagent, with in vitro assays detecting IgG antibodies to Borrelia burgdorferi and IgM antibodies to Borrelia burgdorferi. SEROLOGY LYME DISEASE NEGATIVE CONTROL (LYME CONTROL -) - SR10345
	Lyme Disease Positive Control is intended for use with in vitro assays, for determination of IgG antibodies to Borrelia burgdorferi and IgM antibodies to Borrelia burgdorferi. Lyme Disease Positive Control is unassayed without target values and is suitable for use on many analysers. SEROLOGY LYME DISEASE POSITIVE CONTROL (LYME CONTROL +) - SR10346
	Serology Negative Control is intended for use as an unassayed non-reactive quality assurance reagent with in vitro assays detecting antibody to Human Immunodeficiency Virus Type 1/2 (anti-HIV-1/2), antibody to Human T-Lymphotropic Virus Type I/II (anti-HTLV-I/II), Human Immunodeficiency Virus P24 Antigen (HIV P24 Ag), antibody to Hepatitis C Virus (anti-HCV), Immunoglobulin M and total antibodies to Hepatitis B core Antigen (HBc-IgM and anti-HBc Total), Hepatitis B Surface Antigen (HBsAg), antibody to Hepatitis B Surface Antigen (anti-HBs), Immunoglobulin M and total antibody to Hepatitis A Virus (HAV-IgM and anti-HAV Total), Hepatitis B Envelope Antigen (HBeAg), antibody to Hepatitis B Envelope Antigen (anti-HBe) and antibodies to Treponema pallidum.Serology Negative Control is unassayed without target values and is suitable for use on many analysers. These controls must not be used as a substitute for the mandatory manufacturer’s kit controls provided with the assay.Serology Negative Control is helpful in determining the precision of testing systems and in identifying sources of variation. SEROLOGY NEGATIVE CONTROL (SEROLOGY CONTROL -) - SR10351
	ToRCH EBV Positive Control is intended for use with in vitro assays for determination of IgG and IgM antibodies to the viral capsid antigen of Epstein-Barr Virus (EBV VCA) and IgG antibodies to the viral polypeptide nuclear antigen of Epstein-Barr Virus (EBV EBNA).ToRCH EBV Positive Control is unassayed without target values and is suitable for use on many analysers. This control must not be used as a substitute for the mandatory manufacturer’s kit controls provided with the assay.ToRCH EBV Positive Control is helpful in determining the precision of testing systems and in identifying sources of variation. SEROLOGY ToRCH EBV POSITIVE CONTROL (ToRCH EBV CONTROL +) - SR10350
	ToRCH IgG Positive Control is intended for use with in vitro assays for determination of IgG antibodies to Cytomegalovirus (CMV), IgG antibodies to Rubella Virus, IgG antibodies to Toxoplasma gondii, IgG antibodies to Herpes Simplex Virus Type 1 and 2, IgG antibodies to Mumps Virus, IgG antibodies to Measles Virus, IgG antibodies to Varicella Zoster Virus, IgG antibodies to Helicobacter pylori IgG antibodies to Treponema pallidum (Syphilis), IgG antibodies to the viral polypeptide nuclear antigen of Epstein-Barr Virus (EBV EBNA). ToRCH IgG Positive Control is unassayed without target values and is suitable for use on many analysers. This control must not be used as a substitute for the mandatory manufacturer’s kit controls provided with the assay.ToRCH IgG Positive Control is helpful in determining the precision of testing systems and in identifying sources of variation. SEROLOGY ToRCH IgG POSITIVE CONTROL (ToRCH IgG CONTROL +) - SR10348
	ToRCH IgM Positive Control is intended for use with in vitro assays for determination of IgM antibodies to Cytomegalovirus (CMV), IgM antibodies to Rubella Virus, IgM antibodies to Toxoplasma gondii, IgM antibodies to Herpes Simplex Virus Type 1 and 2.ToRCH IgM Positive Control is unassayed without target values and is suitable for use on many analysers. This control must not be used as a substitute for the mandatory manufacturer’s kit controls provided with the assay.ToRCH IgM Positive Control is helpful in determining the precision of testing systems and in identifying sources of variation. SEROLOGY ToRCH IgM POSITIVE CONTROL (ToRCH IgM CONTROL +) - SR10349
	ToRCH Negative Control is intended for use as an unassayed non-reactive quality assurance reagent with in vitro assays detecting IgG and IgM antibodies to Cytomegalovirus (CMV), IgG and IgM antibodies to Rubella virus, IgG and IgM antibodies to Toxoplasma gondii, IgG and IgM antibodies to Herpes Simplex Type 1 and 2, IgG antibodies to Mumps Virus, IgG antibodies to Rubeola Virus (Measles), IgG antibodies to Varicella Zoster Virus, IgG antibodies to Helicobacter pylori, IgG antibodies to Treponema pallidum (Syphilis), IgG and IgM antibodies to the Viral Capsid Antigen of Epstein-Barr virus (EBV VCA) and IgG antibodies to the Viral Polypeptide Nuclear Antigen of Epstein-Barr Virus (EBV EBNA IgG). SEROLOGY ToRCH NEGATIVE CONTROL (ToRCH CONTROL -) - SR10347
	SERUM DILUENT (DIL SM) SERUM DILUENT (DIL SM) - MS5007
	Intended for in vitro diagnostic (IVD) use to monitor the instrument’s response in detecting haemolyzed, icteric and lipemic samples. SERUM INDICES (SERUM INDICES) - SI10448
	sLDL CALIBRATOR (sLDL CAL) sLDL CALIBRATOR (sLDL CAL) - CH5050
	sLDL CONTROL - LEVEL 1 (sLDL CONTROL 1) sLDL CONTROL - LEVEL 1 (sLDL CONTROL 1) - LE5013
	sLDL CONTROL - LEVEL 2 (sLDL CONTROL 2) sLDL CONTROL - LEVEL 2 (sLDL CONTROL 2) - LE5014
	sLDL CONTROL - LEVEL 3 (sLDL CONTROL 3) sLDL CONTROL - LEVEL 3 (sLDL CONTROL 3) - LE5015
	This should be run once a day to prevent protein build up or at 8 hour intervals if the ISE module performs more than 50 samples per day. Cleaning solution may be aspirated from a sample cup but the cup must be covered between use to eliminate evaporation and ensure accuracy. SOLN WASH - RX4003
	The Randox Soluble Transferrin Receptors Calibrator Series is intended for use in the calibration of Soluble Transferrin Receptors assays. SOLUBLE TRANSFERRIN RECEPTORS CALIBRATOR SERIES (STFR CAL) - TF10161
	The Randox Soluble Transferrin Receptors controls are intended for use, in the control of Soluble Transferrin Receptors assays. SOLUBLE TRANSFERRIN RECEPTORS CONTROLS (STFR CONTROL) - TF10162
	Liquid Protein Calibrators are an in vitro diagnostic product used for the calibration of Alpha-1-Antitrypsin, Alpha-1-Acid glycoprotein, IgA, IgG and IgM assays that require sample pre-dilution. SP CAL (LIQ) - IT2692
	Liquid Protein Calibrators are an in vitro diagnostic product used for the calibration of ASO, Complement C3, Complement C4, Ceruloplasmin, CRP, Ferritin, Haptoglobin, IgA, IgG, IgM, Prealbumin, RF and Transferrin assays. SP CAL (LIQ) - IT2691
	This product is intended for in vitro diagnostic use in the quality control of serum on clinical chemistry and immunoassay systems. The Assayed Liquid Protein Controls are for the control of accuracy. SP CONTROL 1 - PS2682
	This product is intended for in vitro diagnostic use in the quality control of serum on clinical chemistry and immunoassay systems. The Assayed Liquid Protein Controls are for the control of accuracy. SP CONTROL 2 - PS2683
	This product is intended for in vitro diagnostic use in the quality control of serum on clinical chemistry and immunoassay systems. The Assayed Liquid Protein Controls are for the control of accuracy. SP CONTROL 3 - PS2684
	SPECIFIC PROTEIN CONTROL - LEVEL 1 (SP CONTROL 1) SPECIFIC PROTEIN CONTROL - LEVEL 1 (SP CONTROL 1) - PS10221
	SPECIFIC PROTEIN CONTROL - LEVEL 2 (SP CONTROL 2) SPECIFIC PROTEIN CONTROL - LEVEL 2 (SP CONTROL 2) - PS10222
	SPECIFIC PROTEIN CONTROL - LEVEL 3 (SP CONTROL 3) SPECIFIC PROTEIN CONTROL - LEVEL 3 (SP CONTROL 3) - PS10223
	The device is intended for the quantitative in vitro determination of total bilirubin in serum or plasma. T BIL - BR2361
	The device is intended for the quantitative in vitro determination of total bilirubin in serum or plasma. T BIL - BR3859
	The device is intended for the quantitative in vitro determination of total bilirubin in serum or plasma. T BIL - BR8307
	The device is intended for the quantitative in vitro determination of total bilirubin in serum or plasma. T BIL - BR9766
	The TBIL method used on the Dimension clinical chemistry system is an in vitro diagnostic test intended for the quantitative determination of total bilirubin in serum or plasma. T BIL - BR2802
	This product is intended for use in the calibration of therapeutic drug assays. TDM CAL - TD3417
	A Transferrin test system is a device intended for the quantitative in vitro determination of transferrin concentration in serum. TF - TF3831
	Intended for the quantitative in vitro determination of Transferrin in Serum TF - TF7197
	The Cannabinoid assay is an in vitro diagnostic reagent for the qualitative and semi-quantitative analysis of Cannabinoids (THC) in human urine. THC - DA4010
	The Randox Cannabinoid Calibrator Set is intended for use in the calibration of the 11-nor-Δ9-THC-9-COOH (Cannabinoid) assay. THC CAL - DA2700
	The Randox Cannabinoid Control - Level 1 is intended for use in the Quality Control of the 11-nor-Δ9-THC-9-COOH (Cannabinoid) assay. The Cannabinoid Control Level 1 contains the specific drug Cannabinoid. THC CONTROL 1 - DA3127
	The Randox Cannabinoid Control - Level 2 is intended for use in the Quality Control of the 11-nor-Δ9-THC-9-COOH (Cannabinoid) assay. The Cannabinoid Control Level 2 contains the specific drug Cannabinoid. THC CONTROL 2 - DA3128
	For the quantitative in vitro determination of Theophylline in human serum THEO - TD3412
	Therapeutic Drug Markers (TDM) Linearity Verifiers are an in vitro diagnostic product used to assess the linearity of the Roche Systems for Acetaminophen, Amikacin, Carbamazepine, Digoxin, Gentamicin, Lithium, N-Acetylprocainamide, Phenobarbital, Phenytoin, Procainamide, Quinidine, Salicylate, Theophylline, Tobramycin, Valproic Acid and Vancomycin assays. THERAPEUTIC DRUG MARKERS LINEARITY VERIFIERS (For Roche Systems) - LV10355
	For the quantitative in vitro determination of Total Bilirubin in serum and plasma. TOTAL BILIRUBIN 2 (T BIL 2) - BR8377
	A TIBC test system is a device intended for the quantitative in vitro determination of total iron-binding capacity (TIBC) concentration in serum. TOTAL IRON-BINDING CAPACITY 2 (TIBC_2) - TI8065
	A TIBC_2 test system is a device intended for the quantitative in vitro determination of total iron-binding capacity (TIBC) concentration in serum. TOTAL IRON-BINDING CAPACITY 2 (TIBC_2) - TI4064
	A TIBC_2 test system is a device intended for the quantitative in vitro determination of total iron-binding capacity (TIBC) concentration in serum. TOTAL IRON-BINDING CAPACITY 2 (TIBC_2) - TI8375
	For the quantitative in vitro determination of Total Protein in serum and plasma. TOTAL PROTEIN (TP) - TP245
	For the quantitative in vitro determination of Total Protein in serum and plasma. TOTAL PROTEIN (TP) - TP3869
	TOTAL PROTEIN (UP) TOTAL PROTEIN (UP) - UP8113
	For the quantitative in vitro determination of total protein in urine and C.S.F. TOTAL PROTEIN (UP) - UP1570
	TOTAL PROTEIN 2 (TP 2) TOTAL PROTEIN 2 (TP 2) - TP8066
	TOTAL PROTEIN 2 (TP 2) TOTAL PROTEIN 2 (TP 2) - TP8336
	For the quantitative in vitro determination of Total Protein in serum. TOTAL PROTEIN 2 (TP 2) - TP4001
	TOTAL-IRON BINDING CAPACITY (TIBC) TOTAL-IRON BINDING CAPACITY (TIBC) - TI1010
	TOTAL-IRON BINDING CAPACITY (TIBC) TOTAL-IRON BINDING CAPACITY (TIBC) - TI8331
	TRIGLYCERIDES (TRIGS) TRIGLYCERIDES (TRIGS) - TR8067
	TRIGLYCERIDES (TRIGS) TRIGLYCERIDES (TRIGS) - TR8147
	TRIGLYCERIDES (TRIGS) TRIGLYCERIDES (TRIGS) - TR9780
	For the quantitative in vitro determination of Triglycerides in serum and plasma. TRIGLYCERIDES (TRIGS) - TR210
	For the quantitative in vitro determination of triglycerides in serum or plasma. TRIGLYCERIDES (TRIGS) - TR3823
	For the quantitative in vitro determination of Triglycerides in serum or plasma. This product is suitable for Manual use. TRIGLYCERIDES (TRIGS) - TR1697
	For the quantitative in vitro determination of Triglycerides in serum. TRIGLYCERIDES (TRIGS) - TR8332
	This product is intended for in vitro diagnostic use in the quality control of Cardiac Markers on clinical chemistry and Immunoassay systems. TRI-LEVEL CARDIAC CONTROL (CRD CONTROL 1, 2, 3) - CQ3259
	This product is intended for in vitro diagnostic use, in the quality control of Cardiac Markers on clinical chemistry and Immunoassay systems. TRI-LEVEL CARDIAC CONTROL (CRD CONTROL 1, 2, 3) - CQ3100
	The product is intended for the quantitative in vitro determination of Iron/UIBC in serum. UIBC - SI250
	UREA UREA - UR220
	This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine. UREA - UR221
	This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine. UREA - UR3825
	This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine. UREA - UR3873
	This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine. UREA - UR446
	This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine. UREA - UR456
	This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine. UREA - UR457
	This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine. UREA - UR7975
	This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine. UREA - UR7976
	This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine. UREA - UR8334
	This product is intended for the quantitative in vitro determination of Urea in serum, plasma or urine. UREA - UR9729
	URIC ACID (UA) URIC ACID (UA) - UA7972
	URIC ACID (UA) URIC ACID (UA) - UA8069
	URIC ACID (UA) URIC ACID (UA) - UA8333
	For the quantitative in vitro determination of Uric Acid in serum, plasma and urine. URIC ACID (UA) - UA230
	For the quantitative in vitro determination of Uric Acid in serum, plasma and urine. URIC ACID (UA) - UA3824
	For the quantitative in vitro determination of Uric Acid in serum, plasma and urine. URIC ACID (UA) - UA3870
	This product is intended for in vitro diagnostic use, in the quality control of urine test strips. URINALYSIS CONTROL - LEVEL 1 (URNAL CONTROL 1) - UC5033
	This product is intended for in vitro diagnostic use, in the quality control of urine test strips. URINALYSIS CONTROL - LEVEL 2 (URNAL CONTROL 2) - UC5034
	For the quantitative in vitro determination of Valproic Acid in human serum VPA - TD3414
	Cleaning Solution for the RX series analysers WASH conc. 1 - RX3963
	Cleaning Solution for the RX series analysers WASH conc. 2 - RX3962
	Cleaning Solution for the RX series analysers WASH conc. 3 - RX3946
	The Xanthochromia Negative Control is intended for use with in vitro diagnostic assays for the quantitative determination of Bilirubin and Oxyhaemoglobin for monitoring of Subarachnoid-haemorrhage testing in Cerebrospinal Fluid (CSF) for Xanthochromia using a spectrophotometer. Xanthochromia Negative Control is unassayed without target values and is suitable for use on various UV spectrophotometer analysers.Xanthochromia Negative Control is for use by trained laboratory professionals and can be used in determining theprecision of testing systems and in identifying sources of variation. XANTHOCHROMIA NEGATIVE CONTROL (XANTHOCHROMIA ) - XN10502
	The Xanthochromia Positive Control is intended for use with in vitro diagnostic assays for the quantitative determination of Bilirubin and Oxyhaemoglobin for monitoring of Subarachnoid-haemorrhage testing in Cerebrospinal Fluid (CSF) for Xanthochromia using a spectrophotometer. Xanthochromia Positive Control is unassayed, without target values and is suitable for use on various UV spectrophotometer analysers. Xanthochromia Positive Control is for use by trained laboratory professionals and can be used in determining the precision of testing systems and in identifying sources of variation. XANTHOCHROMIA POSITIVE CONTROL (XANTHOCHROMIA ) - XN10505

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