Identity
- Trade Name
- Adenovirus Rapid Test (Feces) EUDAMED
- Device Name
- Adenovirus Rapid Test (colloidal gold method) EUDAMED
- Model / Reference
- Cassette EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06939663977876 EUDAMED
- Basic UDI-DI
- B-06939663977876 EUDAMED
- EMDN Code
- W0105040601 ADENOVIRUS EUDAMED
Classification
- Device Class
- Class IVD General EUDAMED
- Market of Registration
- Germany 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
Adenovirus Rapid Test (Feces) by Sejoy Biomedical 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-06939663977876 | Class IVD General | Active |
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Manufacturer
- Manufacturer
- Sejoy Biomedical Co., Ltd.
- EUDAMED SRN
- CN-MF-000008447
- Authorised Representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Sources (1)
- EUDAMED 22d2a90c-3e5e-464f-b5ad-e5ed3d96555a 61 fields · synced Jul 22, 2026