Identity
- Trade Name
- Alpha Rutschbrett EUDAMED
- Device Name
- Rutschbrett EUDAMED
- Model / Reference
- PM-5050 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04250355350503 EUDAMED
- Basic UDI-DI
- 42503553CRBT50005050N4 EUDAMED
- Direct Marketing DI
- 04250355350503 EUDAMED
- EMDN Code
- Y99 DEVICES FOR PERSONS WITH DISABILITIES NOT INCLUDED IN OTHER CATEGORIES - 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
Alpha Rutschbrett 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 | 42503553CRBT50005050N4 | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Petermann GmbH
- EUDAMED SRN
- DE-MF-000013598
Sources (1)
- EUDAMED 956bdf3c-0d01-4369-8f9c-c98a806ba2a4 61 fields · synced Jun 18, 2026