Identity
- Trade Name
- Anika EUDAMED
- Device Name
- The Anika Complex for Musculoskeletal System Rehabilitation with Biofeedback EUDAMED
- Model / Reference
- 01-1.7 EUDAMED3 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08720299476301 EUDAMED
- Basic UDI-DI
- 87202994763Anika01-1.78A EUDAMED
- Direct Marketing DI
- 08720299476301 EUDAMED
- EMDN Code
- Z12062402 POSITIONAL BIOFEEDBACK SYSTEMS EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
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
Anika by OOO NPF "Rehabilitation technologies" — 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 | 87202994763Anika01-1.78A | Class I | Active |
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Manufacturer
- Manufacturer
- OOO NPF "Rehabilitation technologies"
- EUDAMED SRN
- RU-MF-000001266
- Authorised Representative
- CEpartner4U NL-AR-000000111
Sources (1)
- EUDAMED 9a62f5f3-1248-4384-9516-cf815b3eafdf 61 fields · synced Jul 29, 2026