Identity
- Trade Name
- VIDAS® TOXO IgM EUDAMED
- Device Name
- VIDAS® TOXO IgM EUDAMED
- Model / Reference
- 424641 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03573026634902 EUDAMED
- Basic UDI-DI
- 357302BUDI002209TL EUDAMED
- EMDN Code
- W0105050103 TOXOPLASMA ANTIBODY IGM EUDAMED
Classification
- Device Class
- Class C EUDAMED
- Market of Registration
- France EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Microbial Substances
Yes
EUDAMED
Reagent
Yes
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
New Device
No
EUDAMED
VIDAS® TOXO IgM by Biomerieux Sa — Class C — IVDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 357302BUDI002209TL | Class C | Active |
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Manufacturer
- Manufacturer
- bioMérieux SA
- EUDAMED SRN
- FR-MF-000004436
Sources (2)
- EUDAMED bba9eaf5-3049-4e83-b0e4-af9b154c3b5b 61 fields · synced Sep 30, 2026
- EUDAMED 8117dc2f-e820-4946-bf2a-d529e06b3100 61 fields · synced Jul 8, 2026