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CRP/SAA Control

Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0

Basic Information

Primary DI
06974521000419
Basic UDI-DI Code
B-06974521000419
Reference
QC404
Device Types
None provided
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

The CRP/SAA Control is intended for in vitro diagnostic use in the quality control of the Diagnostic Kit for C-reactive Protein /Serum Amyloid A (Time-resolved Fluorescence Immunochromatographic assay). For in vitro diagnostic use only. For professional use only.

CND Nomenclature Codes

Code Description
W01021521 MULTICOMPONENT IMMUNOCHEMISTRY CONTROLS

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