Ceruloplasmin
ARCHITECT - 6K91-30
Device Description
A collection of reagents and other associated materials intended to be used for the quantitative measurement of ceruloplasmin in a clinical specimen, using a nephelometry/turbidimetry method.
Environmental Conditions
- 29.00
- N/A
- 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: JFR
Device Name: Indirect Copper Assay, Ceruloplasmin
Device Class: 2
Physical State: N/A
Definition: N/A
Submission Type ID: 4
Review Panel: IM
Review Code: N/A
Technical Method: N
Gmp Exempt Flag: N/A
Life Sustain Support Flag: N
Unclassified Reason: N/A
Implant Flag: N
Target Area: N/A
Regulation Number: 866.5210
Third Party Flag: N
Medical Specialty: IM
Device IdentifiersDevice Id: 00380740010829
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