Eu Ivdd Eu Ivd General On The Market 🇹🇷 Türkiye

RapidFor™ Serum Amyloid A Rapid Test Kit (FIA)

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

Basic Information

Primary DI
08683548250407
Basic UDI-DI Code
B-08683548250407
Reference
VMPO29
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 human serum amyloid A (SAA) in human serum, plasma, whole blood.

CND Nomenclature Codes

Code Description
W01021199 RHEUMATOID / INFLAMMATORY DISEASE MARKERS - OTHER

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