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Artiflex - Gel anti-douleur
EUDAMEDClass I (EU MDR)
Ref FV0612Model Artiflex - Tube souple 100 ml
by Noao Sa
Identity
- Trade Name
- Artiflex - Gel anti-douleur EUDAMED
- Device Name
- Artiflex - Gel anti-douleur EUDAMED
- Model / Reference
- Artiflex - Tube souple 100 ml EUDAMEDFV0612 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03701763800001 EUDAMED
- Basic UDI-DI
- 370176380612000D3 EUDAMED
- EMDN Code
- M9002 PROTECTIVE DEVICES, LUBRICANTS AND SOOTHING DEVICES (SPRAYS, GELS, FLUIDS AND CREAMS) 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
Artiflex - Gel anti-douleur by Noao Sa — 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 | 370176380612000D3 | Class I | Active |
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Manufacturer
- Manufacturer
- Noao Sa
- EUDAMED SRN
- FR-MF-000022232
Sources (1)
- EUDAMED 225d6c90-35d5-47ee-b7cf-7569d5800537 61 fields · synced Jun 18, 2026