Identity
- Trade Name
- Περικνημίδα Neoprene XLarge EUDAMED
- Device Name
- Περικνημίδα Neoprene EUDAMED
- Model / Reference
- 05301 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05205414132049 EUDAMED
- Basic UDI-DI
- 5205414053013T EUDAMED
- Direct Marketing DI
- 05205414132049 EUDAMED
- EMDN Code
- Y06120601 PASSIVE ANKLE-FOOT ORTHOSES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Greece 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
Περικνημίδα Neoprene XLarge by Adco Orthopaedics Ltd — 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 | 5205414053013T | Class I | Active |
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Manufacturer
- Manufacturer
- Adco Orthopaedics Ltd
- EUDAMED SRN
- GR-MF-000013663
Sources (1)
- EUDAMED 7626df6e-04d2-4f84-8a49-783a391a2811 61 fields · synced Jul 13, 2026