Eu Ivdd
Eu Ivd General
On The Market
🇹🇷 Türkiye
RapidFor™ Syphilis Ab Rapid Test Kit
Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0
Basic Information
- Primary DI
- 08683347941117
- Basic UDI-DI Code
- B-08683347941117
- Reference
- VMD04
- Device Types
-
Single use
- Regulation
- Eu Ivdd
- Classification
- Eu Ivd General
- Status
- On The Market
- Manufacturer
- Vitrosens Biyoteknoloji Anonim Şirketi
Additional Description
The test is assay for the qualitative detection of the treponema pallidum, antibody in human serum,plasma and whole blood. The test is a screening test, and all positives must be confirmed using an alternate test such as western blot. The test is intended for healthcare professional use only.
CND Nomenclature Codes
| Code | Description |
|---|---|
| W0105090105 | SYPHILIS - RT & POC |
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