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RapidFor™ β2-Microglobulin Rapid Test Kit (FIA)

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

Basic Information

Primary DI
08683548250889
Basic UDI-DI Code
B-08683548250889
Reference
VMPO50
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

This kit is suitable for in vitro quantitative detection of β2 microglobulin (β2-MG) concentration in human serum, whole blood, plasma and urine samples.

CND Nomenclature Codes

Code Description
W0102039002 BETA2-MICROGLOBULIN

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