← Back to catalogue
Guiding tube L long StemExtractor
EUDAMEDClass I (EU MDR)
Ref 780609 endocon catalogueModel Arthroplasty revision system
by endocon GmbH
Identity
- Trade Name
- Guiding tube L long StemExtractor EUDAMED
- Device Name
- Revisionsinstrumentensystem EUDAMED
- Model / Reference
- Arthroplasty revision system EUDAMED780609 endocon catalogue EUDAMED
Identifiers
- Primary DI / UDI-DI
- 42514018026496 EUDAMED
- Basic UDI-DI
- 4251401801512Q3 EUDAMED
- Direct Marketing DI
- 42514018026496 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 L long 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 b0adc2c6-3114-4fa6-a83f-29b41684b2cb 61 fields · synced Jun 19, 2026