Eu Ivdd
Eu Ivd General
On The Market
🇨🇳 China
Syphilis Rapid Test Device (serum/plasma/whole blood)
Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0
Basic Information
- Primary DI
- 06976753474631
- Basic UDI-DI Code
- B-06976753474631
- Reference
- A300501D
- Device Types
-
Single use
- Regulation
- Eu Ivdd
- Classification
- Eu Ivd General
- Status
- On The Market
- Manufacturer
- Hangzhou Cybereagen Biotech Co., Ltd.
Additional Description
Syphilis Rapid Test Device (serum/plasma/whole blood) is a rapid chromatographic immunoassay for the qualitative detection of antibodies to Treponema Pallidum in serum or plasma or whole blood.
CND Nomenclature Codes
| Code | Description |
|---|---|
| W0105010301 | SYPHILIS ANTIGEN DETECTION |
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