Identity
- Trade Name
- A2® Eröffnungsraspel EUDAMED
- Device Name
- Klasse Ir Instrumente, allgemeine chirurgisch invasive Instrumente des A2® Hüftschaftsystems, wiederverwendbar; sonstige wiederverwendbare invasive Instrumente EUDAMED
- Model / Reference
- 9110100 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04251143406198 EUDAMED
- Basic UDI-DI
- 42511434011001BK EUDAMED
- Direct Marketing DI
- 04251143406198 EUDAMED
- EMDN Code
- L091201 ORTHOPAEDIC SURGERY RASPS, 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
A2® Eröffnungsraspel by ARTIQO 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 | 42511434011001BK | Class I | Active |
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Manufacturer
- Manufacturer
- ARTIQO GmbH
- EUDAMED SRN
- DE-MF-000007336
Sources (1)
- EUDAMED 964f1f05-c43f-4d00-b5ce-d67b4ae0de39 61 fields · synced Jul 12, 2026