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BORRELIA VIRCLIA® IgM MONOTEST

EUDAMED

Class B (EU MDR)

Ref VCM010

by Vircell, S.L

Identity

Trade Name
BORRELIA VIRCLIA® IgM MONOTEST EUDAMED
Device Name
BORRELIA VIRCLIA® IgM MONOTEST EUDAMED
Model / Reference
VCM010 EUDAMED

Identifiers

Primary DI / UDI-DI
08436040326671 EUDAMED
Basic UDI-DI
843604032VCM01001BC EUDAMED
EMDN Code
W0105010604 LYME ANTIBODY IGM EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

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

BORRELIA VIRCLIA® IgM MONOTEST 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 a2cb86cb-f586-436f-ae4b-6272fa1587cf 61 fields · synced Jul 27, 2026