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Arthroplasty revision system
EUDAMEDClass I (EU MDR)
Ref 780899Model Arthroplasty revision system
by endocon GmbH
Identity
- Trade Name
- Arthroplasty revision system EUDAMED
- Device Name
- Revisionsinstrumentensystem EUDAMED
- Model / Reference
- Arthroplasty revision system EUDAMED780899 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 42514018032190 EUDAMED
- Basic UDI-DI
- 4251401801512Q3 EUDAMED
- Direct Marketing DI
- 42514018032190 EUDAMED
- EMDN Code
- L0399 GENERAL SURGERY 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
Yes
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Arthroplasty revision system by endocon 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 | 4251401801512Q3 | Class I | Active |
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Manufacturer
- Manufacturer
- endocon GmbH
- EUDAMED SRN
- DE-MF-000020703
Sources (1)
- EUDAMED 9e5c84d3-6d6a-410d-abd4-2bd21642d1d7 61 fields · synced Jul 11, 2026