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Treponema Pallidum Antibodies Kit(CLIA)

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

Basic Information

Primary DI
06936595751703
Basic UDI-DI Code
B-06936595751703
Reference
FG1506Y
Device Types
None provided
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

For the qualitative detection of treponema pallidum antibodies (Anti-TP) in human serum or plasma. For laboratory professional in vitro diagnostic use.

CND Nomenclature Codes

Code Description
W0105010302 SYPHILIS ANTIBODY ASSAYS TOTAL

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