Identity
- Trade Name
- Beingurt Erweiterung EUDAMEDBeingurt EUDAMED
- Device Name
- Beingurt EUDAMED
- Model / Reference
- PM-3007 EUDAMEDPM-3005 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04250355330079 EUDAMED04250355330055 EUDAMED
- Basic UDI-DI
- 42503553MBGT75103007SG EUDAMED
- Direct Marketing DI
- 04250355330079 EUDAMED04250355330055 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
Beingurt Erweiterung 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 | 42503553MBGT75103007SG | Class I | Active |
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Manufacturer
- Manufacturer
- Petermann GmbH
- EUDAMED SRN
- DE-MF-000013598
Sources (2)
- EUDAMED 03d68190-0b00-4c7a-8c9d-de5fb321df2f 61 fields · synced Jun 20, 2026
- EUDAMED f565c039-91e7-472c-813c-3d8ca990c84f 61 fields · synced May 18, 2026