Eu Ivdd Eu Ivd General On The Market 🇹🇷 Türkiye

RapidFor™ CK-MB Rapid Test Kit

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

Basic Information

Primary DI
08683347941575
Basic UDI-DI Code
B-08683347941575
Reference
VMD51
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

The RapidFor™ CK-MB Rapid Test Kit is designed for the detection of creatine kinase-MB (CK-MB) protein in human serum, plasma and whole blood samples.

CND Nomenclature Codes

Code Description
W0102160799 CARDIAC MARKERS - RT & POC - OTHER

Similar Devices

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

View all