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4-motion® Probefemur links 8w
EUDAMEDClass IIa (EU MDR)
Ref 9210709
by ARTIQO GmbH
Identity
- Trade Name
- 4-motion® Probefemur links 8w EUDAMED
- Device Name
- Klasse IIa Instrumente, chirurgisch invasiv, wiederverwendbar; Probeimplantate EUDAMED
- Model / Reference
- 9210709 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04251143403333 EUDAMED
- Basic UDI-DI
- 42511434022002C7 EUDAMED
- Direct Marketing DI
- 04251143403333 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
4-motion® Probefemur links 8w 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 | 42511434022002C7 | Class IIa | Active |
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Manufacturer
- Manufacturer
- ARTIQO GmbH
- EUDAMED SRN
- DE-MF-000007336
Sources (1)
- EUDAMED cf1271c3-20e0-4b1b-8c32-58b41a743e69 61 fields · synced Jun 19, 2026