Identity
- Device Name
- Venoflex Kokoon Absolu EUDAMED
- Model / Reference
- 52300320004312 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03111790055242 EUDAMED
- Basic UDI-DI
- 311179FR0003CEB EUDAMED
- Direct Marketing DI
- 03111790055242 EUDAMED
- EMDN Code
- M030405 COMPRESSION STOCKINGS 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
Venoflex Kokoon Absolu by Thuasne — 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 | 311179FR0003CEB | Class I | Active |
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Manufacturer
- Manufacturer
- Thuasne
- EUDAMED SRN
- FR-MF-000001201
Sources (1)
- EUDAMED c4ae8128-02b8-4a36-9813-3aded93206fa 61 fields · synced Jun 18, 2026