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Retractor set
EUDAMEDClass I (EU MDR)
Ref 9100070 endocon catalogueModel Arthroplasty revision system
by endocon GmbH
Identity
- Trade Name
- Retractor set EUDAMED
- Device Name
- Revisionsinstrumentensystem EUDAMED
- Model / Reference
- Arthroplasty revision system EUDAMED9100070 endocon catalogue EUDAMED
Identifiers
- Primary DI / UDI-DI
- 42514018038994 EUDAMED
- Basic UDI-DI
- 4251401801512Q3 EUDAMED
- Direct Marketing DI
- 42514018038994 EUDAMED
- EMDN Code
- L0915 SPREADERS AND RETRACTORS FOR ORTHOPAEDIC SURGERY, REUSABLE 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
Retractor set 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 cde5e62e-c3e9-4ab1-97c6-3084784c74f2 61 fields · synced Jul 9, 2026