Identity
- Trade Name
- VISIOLITE EUDAMED
- Device Name
- VISIOLITE MASTER GT EUDAMED
- Model / Reference
- VISIOLITE EUDAMEDFF1055 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03760253450089 EUDAMED
- Basic UDI-DI
- 376025345FF1017TE EUDAMED
- Direct Marketing DI
- 03760253450089 EUDAMED
- EMDN Code
- Z1212012001 VISUAL FUNCTIONAL ASSESSMENT EQUIPMENT 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
Visiolite by FIM Medical — 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 | 376025345FF1017TE | Class I | Active |
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Manufacturer
- Manufacturer
- FIM Médical
- EUDAMED SRN
- FR-MF-000017090
Sources (1)
- EUDAMED e75ed11f-5068-46f5-8af1-76d3aefb938d 61 fields · synced May 22, 2026