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RapidFor™CRP/SAA Rapid Test Kit (FIA)

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

Basic Information

Primary DI
08683548250957
Basic UDI-DI Code
B-08683548250957
Reference
VMPO57
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

This test is suitable for in vitro quantitative detection of the concentration of C-reactive protein and human serum amyloid A in human serum, plasma, whole blood.

CND Nomenclature Codes

Code Description
W0102019012 AMYLOID BETA-DERIVED DIFFUSIBLE LIGAND (BETA-AMYLOID OLIGOMER)
W0102160601 C-REACTIVE PROTEIN - RT & POC

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