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DELFIA Xpress

EUDAMED

Class A (EU MDR)

Ref 6000-0010

by Wallac Oy

Identity

Trade Name
DELFIA Xpress EUDAMED
Device Name
DELFIA Xpress EUDAMED
Model / Reference
6000-0010 EUDAMED

Identifiers

Primary DI / UDI-DI
06438147217328 EUDAMED
Basic UDI-DI
6438147DELFIA_XpressHQ EUDAMED
EMDN Code
W0201020101 AUTOMATED IMMUNOCHEMISTRY ANALYSERS - LOW ROUTINE (Throughput <= 100 test/h) 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

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

DELFIA Xpress 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 7108e22c-344d-47d5-b38d-096b3f1e564c 61 fields · synced Jun 18, 2026