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Rotaflow Centrifugal Pump (RF-32)
EUDAMEDClass IIa (EU MDR)
Ref 701077189Model RF-32
Identity
- Trade Name
- Rotaflow Centrifugal Pump (RF-32) EUDAMED
- Device Name
- Rotaflow Centrifugal Pump (RF-32) EUDAMED
- Model / Reference
- RF-32 EUDAMED701077189 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04058863307732 EUDAMED
- Basic UDI-DI
- 405886330773DD EUDAMED
- Direct Marketing DI
- 04058863307732 EUDAMED
- EMDN Code
- C030199 EXTRACORPOREAL AND ASSISTED CIRCULATION DEVICES - OTHER EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Rotaflow Centrifugal Pump (RF-32) by Maquet Cardiopulmonary GmbH — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 405886330773DD | Class IIa | Active |
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Manufacturer
- Manufacturer
- Maquet Cardiopulmonary GmbH
- EUDAMED SRN
- DE-MF-000020091
Sources (1)
- EUDAMED 3f88ef66-abb8-4a60-a37b-80e0d4378ec7 61 fields · synced Jun 8, 2026