Eu Ivdd Eu Ivd General On The Market 🇹🇷 Türkiye

RapidFor™ CRP Rapid Test Kit (FIA)

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

Basic Information

Primary DI
08683548250186
Basic UDI-DI Code
B-08683548250186
Reference
VMPO10
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 in human serum, plasma, and whole blood. This product is provided for testing by medical and health institutions and is used for auxiliary diagnosis of patients' inflammation and other related diseases.

CND Nomenclature Codes

Code Description
W0102160601 C-REACTIVE PROTEIN - RT & POC

Similar Devices

Other on-the-market devices with the same classification (Eu Ivd General) and regulation (EU IVDD).

View all