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RHOTON Dissektor Fig. 3 TI
EUDAMEDClass I (EU MDR)
Ref 99-9011-83Model Separator, Dura
Identity
- Trade Name
- RHOTON Dissektor Fig. 3 TI EUDAMED
- Model / Reference
- Separator, Dura EUDAMED99-9011-83 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04250379968708 EUDAMED
- Basic UDI-DI
- 4250485300000132Z7 EUDAMED
- Direct Marketing DI
- 04250379968708 EUDAMED
- EMDN Code
- L01040701 DURA MATER SCISSORS, 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
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
RHOTON Dissektor Fig. 3 TI by Zepf Medical Instruments 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 | 4250485300000132Z7 | Class I | Active |
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Manufacturer
- Manufacturer
- Zepf Medical Instruments GmbH
- EUDAMED SRN
- DE-MF-000005528
Sources (1)
- EUDAMED 67758a98-d665-4402-838d-7e18b2fc31ab 61 fields · synced Sep 30, 2026