Identity
- Trade Name
- GENEDIAN EUDAMED
- Device Name
- SARS-CoV-2 Neutralization Antibody Detection Kit EUDAMED
- Model / Reference
- L121-10120 EUDAMED
Identifiers
- Primary DI / UDI-DI
- D-RA008UR EUDAMED
- Basic UDI-DI
- B-RA008UR EUDAMED
- EMDN Code
- W0105040619 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
Yes
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
Genedian by Hangzhou DIAN Biotechnology 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-RA008UR | Class IVD General | Active |
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Manufacturer
- Manufacturer
- Hangzhou DIAN Biotechnology Co., Ltd.
- EUDAMED SRN
- CN-MF-000007252
- Authorised Representative
- Lotus NL B.V. NL-AR-000000121
Sources (1)
- EUDAMED b046f44c-445d-4fe1-aef7-ed5527e5b856 61 fields · synced Jun 19, 2026