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Cryostab® Orthotape Articulee
EUDAMEDClass I (EU MDR)
Ref CRYOSTAB® ORTHOTAPE ARTICULEE
Identity
- Trade Name
- CRYOSTAB® ORTHOTAPE ARTICULEE EUDAMED
- Device Name
- CRYOSTAB® ORTHOTAPE ARTICULEE EUDAMED
- Model / Reference
- CRYOSTAB® ORTHOTAPE ARTICULEE EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03760035448907 EUDAMED
- Basic UDI-DI
- 376003544GENCRY008STBU EUDAMED
- EMDN Code
- Y061209 KNEE ORTHOSES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- France 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
Cryostab® Orthotape Articulee by Groupe Sober Sas — 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 | 376003544GENCRY008STBU | Class I | Active |
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Manufacturer
- Manufacturer
- Groupe Sober Sas
- EUDAMED SRN
- FR-MF-000017818
Sources (1)
- EUDAMED e591a6c6-c7a4-48ae-bcec-3c23435022e5 61 fields · synced Jun 19, 2026