Eu Ivdd
Eu Ivd General
On The Market
🇨🇳 China
CEA Rapid Quantitative Test
Devices (same UDI-DI)
1
Certificates
0
Countries
0
Notified Bodies
0
Basic Information
- Primary DI
- 06933260208555
- Basic UDI-DI Code
- B-06933260208555
- Reference
- BT2401
- Device Types
-
Single use
- Regulation
- Eu Ivdd
- Classification
- Eu Ivd General
- Status
- On The Market
- Manufacturer
- Xiamen Biotime Biotechnology Co., Ltd.
Additional Description
The Biotime CEA (Carcinoembryonic antigen) Rapid Quantitative Test along with Biotime FIA Analyzer is intended to quantify the concentration of CEA in human serum or plasma by fluorescence immunoassay. It is used as a detection of disease monitoring of tumor patients after radiation therapy or surgery.
CND Nomenclature Codes
| Code | Description |
|---|---|
| W0102030112 | CARCINOEMBRYONIC ANTIGEN |
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