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Pro SARS-CoV-2 Ag Rapid Test
EUDAMEDClass IVD General (EU MDR)
Ref VCD16-01Model VCD16
Identity
- Trade Name
- Pro SARS-CoV-2 Ag Rapid Test EUDAMED
- Device Name
- Pro SARS-CoV-2 Ag Rapid Test EUDAMED
- Model / Reference
- VCD16 EUDAMEDVCD16-01 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06937339210333 EUDAMED
- Basic UDI-DI
- B-06937339210333 EUDAMED
- EMDN Code
- W0105090501 CORONAVIRUS ANTIGEN (AG) - RT & POC EUDAMED
Classification
- Device Class
- Class IVD General EUDAMED
- Market of Registration
- Italy EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
Yes
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
Pro SARS-CoV-2 Ag Rapid Test by VivaChek Biotech (Hangzhou) Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-06937339210333 | Class IVD General | Active |
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Manufacturer
- Manufacturer
- VivaChek Biotech (Hangzhou) Co., Ltd.
- EUDAMED SRN
- CN-MF-000012160
- Authorised Representative
- Lotus NL B.V. NL-AR-000000121
Sources (1)
- EUDAMED c313014a-d632-4a88-a722-d6edb5bc7292 61 fields · synced Jul 20, 2026