Identity
- Device Name
- Motimove-8 EUDAMED
- Model / Reference
- MM8 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08607000348709 EUDAMED
- Basic UDI-DI
- B-08607000348709 EUDAMED
- EMDN Code
- Z12062702,Z12062703 EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- France EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Motimove-8 by 3F-Fit Fabricando Faber d.o.o. Beograd-Čukarica — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-08607000348709 | Class IIa | Active |
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Manufacturer
- Manufacturer
- 3F-Fit Fabricando Faber d.o.o. Beograd-Čukarica
- EUDAMED SRN
- RS-MF-000020496
- Authorised Representative
- Salus Cons Kft. HU-AR-000006177
Sources (1)
- EUDAMED eb4f9da1-b252-4436-a2c8-a72b21b2934d 61 fields · synced Jun 18, 2026