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DELFIA hCG

EUDAMED

Class IVD Annex II List B (EU MDR)

Ref A082-101

by Wallac Oy

Identity

Trade Name
DELFIA hCG EUDAMED
Device Name
DELFIA hCG EUDAMED
Model / Reference
A082-101 EUDAMED

Identifiers

Primary DI / UDI-DI
06438147121533 EUDAMED
Basic UDI-DI
B-06438147121533 EUDAMED
EMDN Code
W0102050205 TOTAL HUMAN CHORIONIC GONADOTROPIN EUDAMED

Classification

Device Class
Class IVD Annex II List B EUDAMED
Market of Registration
Finland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

EUDAMED

Animal Tissues

Yes

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

DELFIA hCG by Wallac Oy — Class IVD Annex II List B — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

Manufacturer
Wallac Oy
EUDAMED SRN
FI-MF-000022620

Sources (1)

  • EUDAMED f7edc7a1-8d83-4fbb-a0f1-7cd95c04a92c 61 fields · synced May 22, 2026