Eu Ivdd Eu Ivd General On The Market 🇨🇳 China

Syphilis Antibody Rapid Test

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

Basic Information

Primary DI
06974238910667
Basic UDI-DI Code
B-06974238910667
Reference
HTP063T
Device Types
Single use
Regulation
Eu Ivdd
Classification
Eu Ivd General
Status
On The Market

Additional Description

Syphilis Antibody Rapid Test is a rapid chromatographic immunoassay for the qualitative detection of antibodies (IgG and IgM) to Treponema Pallidum (TP) in whole blood, serum or plasma to aid in the diagnosis of Syphilis.

CND Nomenclature Codes

Code Description
W0105010302 SYPHILIS ANTIBODY ASSAYS TOTAL

Similar Devices

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

View all