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ARLT Draht Schlinge gerieft
EUDAMEDClass I (EU MDR)
Ref 42-4409-02Model Schlingeninstrument, sonstige
Identity
- Trade Name
- ARLT Draht Schlinge gerieft EUDAMED
- Model / Reference
- Schlingeninstrument, sonstige EUDAMED42-4409-02 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04250379895592 EUDAMED
- Basic UDI-DI
- 425048530000028524 EUDAMED
- Direct Marketing DI
- 04250379895592 EUDAMED
- EMDN Code
- L1799 OPHTHALMOLOGY 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
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
ARLT Draht Schlinge gerieft 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 | 425048530000028524 | Class I | Active |
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Manufacturer
- Manufacturer
- Zepf Medical Instruments GmbH
- EUDAMED SRN
- DE-MF-000005528
Sources (1)
- EUDAMED 6f80af6a-dd60-45f3-baa5-51ca3e4c5159 61 fields · synced Sep 17, 2026