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Vanadis Core Buffer kit v2

EUDAMED

Class A (EU MDR)

Ref 3223-0020

by Wallac Oy

Identity

Trade Name
Vanadis Core Buffer kit v2 EUDAMED
Device Name
Vanadis Core Buffer kit v2 EUDAMED
Model / Reference
3223-0020 EUDAMED

Identifiers

Primary DI / UDI-DI
06438147393701 EUDAMED
Basic UDI-DI
6438147Vanadis_Buffer2VW EUDAMED
EMDN Code
W010699 GENETIC TESTS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

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

Yes

EUDAMED

Vanadis Core Buffer kit v2 by Wallac Oy — Class A — 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
Wallac Oy
EUDAMED SRN
FI-MF-000022620

Sources (1)

  • EUDAMED f9919401-9548-4bd0-99c6-87270b88b9aa 61 fields · synced Jun 19, 2026