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HAV IgM Rapid Test

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

Basic Information

Primary DI
16972698600156
Basic UDI-DI Code
B-16972698600156
Reference
P231103
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

The HAV IgM Rapid Test is used for in vitro qualitative detection of Hepatitis A IgM antibody in human whole blood /serum/plasma. For professional use only. (40 tests/kit)

CND Nomenclature Codes

Code Description
W0105090299 HEPATITIS VIRUSES - RT & POC - OTHER

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