Identity
- Trade Name
- Manipulierhals Raspel EUDAMED
- Device Name
- Klasse IIa Instrumente, chirurgisch invasiv, wiederverwendbar; Probeimplantate des A2® Hüftschaftsystems EUDAMED
- Model / Reference
- 9110601 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04251143406310 EUDAMED
- Basic UDI-DI
- 42511434021002BY EUDAMED
- Direct Marketing DI
- 04251143406310 EUDAMED
- EMDN Code
- L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED
Classification
- Device Class
- Class IIa 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
Manipulierhals Raspel by ARTIQO GmbH — Class IIa — 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 | 42511434021002BY | Class IIa | Active |
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Manufacturer
- Manufacturer
- ARTIQO GmbH
- EUDAMED SRN
- DE-MF-000007336
Sources (1)
- EUDAMED 1d8db4dc-2a4e-4961-b77e-1db3e4d4f040 61 fields · synced Jul 21, 2026