Identity
- Trade Name
- Keil EUDAMEDKeil hart EUDAMED
- Device Name
- Positionierung EUDAMED
- Model / Reference
- PM-8017 EUDAMEDPM-8017-h EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04250355380173 EUDAMED04250355381170 EUDAMED
- Basic UDI-DI
- 42503553FPOS801080505M EUDAMED
- Direct Marketing DI
- 04250355380173 EUDAMED04250355381170 EUDAMED
- EMDN Code
- V0899 MEDICAL SUPPORT EQUIPMENT - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
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
Keil by Petermann GmbH — Class I — 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 | 42503553FPOS801080505M | Class I | Active |
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Manufacturer
- Manufacturer
- Petermann GmbH
- EUDAMED SRN
- DE-MF-000013598
Sources (2)
- EUDAMED 8da6258c-72c3-4f78-a4e3-63f8d887786c 61 fields · synced Aug 4, 2026
- EUDAMED ab42d782-5bcf-4286-a6bb-1b65aa6e8f81 61 fields · synced May 17, 2026