Alinity m CMV AMP Kit
Alinity m - 09N46-095
Device Description
A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of nucleic acid from cytomegalovirus (CMV) in a clinical specimen, using a nucleic acid technique (NAT).
Environmental Conditions
- 8.00
- 2.00
Device Sizes
No Data Available
Device Sterilization
Device Sterile: False
Sterilization Prior To Use: False
Sterilization Methods: No Data Available
Product Codes
Code: PAB
Device Name: Cytomegalovirus (Cmv) Dna Quantitative Assay
Device Class: 2
Physical State: IVD
Definition: Cytomegalovirus (CMV) DNA Quantitative Assay is an in vitro nucleic acid assay for the quantitative measurement of CMV DNA in human plasma. The assay can be used to measure CMV DNA levels serially at baseline and during the course of antiviral treatment to assess virological response to treatment. The test results must be interpreted within the context of all relevant clinical and laboratory findings.
Submission Type ID: 1
Review Panel: MI
Review Code: N/A
Technical Method: N
Gmp Exempt Flag: In vitro nucleic acid based assay using real-time PCR for the quantitative measurement of CMV DNA
Life Sustain Support Flag: N
Unclassified Reason: N/A
Implant Flag: N
Target Area: Not Applicable
Regulation Number: 866.3180
Third Party Flag: N
Medical Specialty: MI
Device IdentifiersDevice Id: 00884999049611
Device Type: Primary
DeviceId Issuing Agency: GS1
Contains DI Number: N/A
Package Quantity: N/A
Package Discontinue Date: N/A
Package Status: N/A
Package Type: N/A