Identity
- Trade Name
- iFuge D08 EUDAMED
- Device Name
- Doctor Centrifuge iFuge D08 EUDAMED
- Model / Reference
- iFuge D08 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 89080197330200 EUDAMED
- Basic UDI-DI
- 8908019733D08CD EUDAMED
- EMDN Code
- W02069003 CENTRIFUGES EUDAMED
Classification
- Device Class
- Class A EUDAMED
- Market of Registration
- Germany 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
Category: General-purpose centrifuge IVD
iFuge D08 by Accumax Lab Devices Private Limited — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS
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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 | 8908019733D08CD | Class A | Active |
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Manufacturer
- Manufacturer
- Accumax Lab Devices Private Limited
- EUDAMED SRN
- IN-MF-000028076
- Authorised Representative
- mdi Europa GmbH DE-AR-000006218
Sources (1)
- EUDAMED ee526efc-4927-4f5f-852a-d8e819c07c5a 61 fields · synced Jun 18, 2026