Identity
- Trade Name
- VIDAS® EBV VCA/EA IgG EUDAMED
- Device Name
- VIDAS® EBV VCA/EA IgG EUDAMED
- Model / Reference
- 30236 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03573026064617 EUDAMED
- Basic UDI-DI
- 357302BUDI000080T2 EUDAMED
- EMDN Code
- W010504040105 EBV VCA IGG EUDAMED
Classification
- Device Class
- Class B EUDAMED
- Market of Registration
- France EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
Yes
EUDAMED
Animal Tissues
No
EUDAMED
Microbial Substances
No
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® EBV VCA/EA IgG by Biomerieux Sa — Class B — 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 | 357302BUDI000080T2 | Class B | Active |
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Manufacturer
- Manufacturer
- bioMérieux SA
- EUDAMED SRN
- FR-MF-000004436
Sources (1)
- EUDAMED 0a2fb63e-0855-421e-914e-e96631859203 61 fields · synced Jun 19, 2026