Eu Ivdd Eu Ivd General On The Market 🇹🇷 Türkiye

RapidFor™Myoglobin Rapid Test Kit (FIA)

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

Basic Information

Primary DI
08683548250209
Basic UDI-DI Code
B-08683548250209
Reference
VMPO12
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 myoglobin 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
W0102160702 MYOGLOBIN - RT & POC

Similar Devices

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

View all