Identity
- Trade Name
- AFI EUDAMED
- Device Name
- 230V / 50Hz IVD QBD REGINA EUDAMED
- Model / Reference
- AFI-C1200R-E-QBD/IVD EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03760369880220 EUDAMED
- Basic UDI-DI
- 376036988C1200R-E-QBDF2 EUDAMED
- Direct Marketing DI
- 03760369880220 EUDAMED
- EMDN Code
- W02069005 REFRIGERATED CENTRIFUGES EUDAMED
Classification
- Device Class
- Class A EUDAMED
- Market of Registration
- France EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Microbial Substances
No
EUDAMED
Reagent
No
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
No
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
New Device
No
EUDAMED
Afi by AFI Centrifuge — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 376036988C1200R-E-QBDF2 | Class A | Active |
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Manufacturer
- Manufacturer
- AFI Centrifuge
- EUDAMED SRN
- FR-MF-000001636
Sources (1)
- EUDAMED 18f5edad-a86b-4fa9-b635-ff1d8e0d50b8 61 fields · synced Jun 18, 2026