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DELFIA Xpress uE3

EUDAMED

Class IVD Annex II List B (EU MDR)

Ref 6005-0010Ref 6005-001C

by Wallac Oy

Identity

Trade Name
DELFIA Xpress uE3 EUDAMED
Device Name
DELFIA Xpress uE3 EUDAMED
Model / Reference
6005-0010 EUDAMED
6005-001C EUDAMED

Identifiers

Primary DI / UDI-DI
06438147244553 EUDAMED
06438147252404 EUDAMED
Basic UDI-DI
B-06438147244553 EUDAMED
B-06438147252404 EUDAMED
EMDN Code
W0102050203 UNCONJUGATED (FREE) ESTRIOL 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 Xpress uE3 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 (2)

  • EUDAMED 7cafb073-1d61-4ced-9f19-ce6793867173 61 fields · synced Jul 20, 2026
  • EUDAMED 6fb113cf-6a12-45d1-9562-c56fbf13f036 61 fields · synced May 18, 2026