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VIRAPID® ADENOVIRUS Ag FIA

EUDAMED

Class B (EU MDR)

Ref VRF001

by Vircell, S.L

Identity

Trade Name
VIRAPID® ADENOVIRUS Ag FIA EUDAMED
Device Name
VIRAPID® ADENOVIRUS Ag FIA EUDAMED
Model / Reference
VRF001 EUDAMED

Identifiers

Primary DI / UDI-DI
08436610290593 EUDAMED
Basic UDI-DI
843661029VRF00101QR EUDAMED
EMDN Code
W0105099099 VIROLOGY - RT & POC - OTHER EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

VIRAPID® ADENOVIRUS Ag FIA by Vircell, S.L — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
Vircell, S.L
EUDAMED SRN
ES-MF-000004099

Sources (1)

  • EUDAMED f62c34a5-1c42-4db9-b3ca-a9d7a373781a 61 fields · synced Jul 21, 2026