← Back to catalogue
Guiding tube ST StemExtractor
EUDAMEDClass I (EU MDR)
Ref 780611 endocon catalogue Model Arthroplasty revision system
by endocon GmbH
Identity
- Trade Name
- Guiding tube ST StemExtractor EUDAMED
- Device Name
- Revisionsinstrumentensystem EUDAMED
- Model / Reference
- Arthroplasty revision system EUDAMED780611 endocon catalogue EUDAMED
Identifiers
- Primary DI / UDI-DI
- 42514018025406 EUDAMED
- Basic UDI-DI
- 4251401801512Q3 EUDAMED
- Direct Marketing DI
- 42514018025406 EUDAMED
- EMDN Code
- L091101 ORTHOPAEDIC PROSTHESES AND TRAUMATOLOGICAL IMPLANTS EXTRACTORS, 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
Guiding tube ST StemExtractor 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- endocon GmbH
- EUDAMED SRN
- DE-MF-000020703
Sources (1)
- EUDAMED 0cb4ff00-050b-4701-a304-65c1e021bba5 61 fields · synced Jun 18, 2026