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Phadia Xplain

EUDAMED

Class B (EU MDR)

Ref 81-1013-01

by Phadia AB

Identity

Trade Name
Phadia Xplain EUDAMED
Device Name
Phadia Xplain EUDAMED
Model / Reference
81-1013-01 EUDAMED

Identifiers

Primary DI / UDI-DI
07333066021126 EUDAMED
Basic UDI-DI
7333066BUDI0033LV EUDAMED
EMDN Code
W0201020192 AUTOMATED IMMUNOCHEMISTRY ANALYSERS - IVD MEDICAL DEVICE SOFTWARE EUDAMED

Classification

Device Class
Class B EUDAMED
Special Device Type
Software EUDAMED
Market of Registration
Sweden 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

No

EUDAMED

New Device

No

EUDAMED

Phadia Xplain by Phadia AB — 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
Phadia AB
EUDAMED SRN
SE-MF-000014170

Sources (1)

  • EUDAMED b5ffe211-2095-4325-8d7d-bb7f7dcb2d6a 61 fields · synced Jun 19, 2026