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RapidFor™CK-MB Rapid Test Kit (FIA)

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

Basic Information

Primary DI
08683548250292
Basic UDI-DI Code
B-08683548250292
Reference
VMPO18
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 creatine kinase MB isoenzyme(CK-MB) in human serum, plasma and whole blood. This product is used for testing in medical and health institutions for the auxiliary diagnosis of myocardial infarction.

CND Nomenclature Codes

Code Description
W01010114 CREATINE KINASE - MB ACTIVITY (CC)

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