Identity
- Trade Name
- Reduzierhülse K-Draht EUDAMED
- Device Name
- MRS-TITAN Standard/Maximum Instruments EUDAMED
- Model / Reference
- 54600-12 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04051308034248 EUDAMED
- Basic UDI-DI
- 4029839PB00000247F EUDAMED
- EMDN Code
- L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
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
Reduzierhülse K-Draht by Peter Brehm 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 | 4029839PB00000247F | Class I | Active |
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Manufacturer
- Manufacturer
- Peter Brehm GmbH
- EUDAMED SRN
- DE-MF-000006458
Sources (1)
- EUDAMED 57d7c77f-cf79-4e1f-b6bf-bc58bc2b67a9 61 fields · synced Sep 17, 2026