Identity
- Trade Name
- Venoline FAS EUDAMED
- Device Name
- Venoline FAS EUDAMED
- Model / Reference
- VN702XRR EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07331004702243 EUDAMED
- Basic UDI-DI
- 7331004770206J EUDAMED
- Direct Marketing DI
- 07331004702243 EUDAMED
- EMDN Code
- M030405 COMPRESSION STOCKINGS EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Sweden 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
Venoline FAS by Inverdia AB — 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 | 7331004770206J | Class I | Active |
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Manufacturer
- Manufacturer
- Inverdia AB
- EUDAMED SRN
- SE-MF-000047520
Sources (1)
- EUDAMED 07536222-32b3-43aa-b6b8-38079546fe32 61 fields · synced Jun 18, 2026