← Back to catalogue

EliA Mi-2 Well

EUDAMED

Class B (EU MDR)

Ref 14-5604-01

by Phadia AB

Identity

Trade Name
EliA Mi-2 Well EUDAMED
Device Name
EliA Mi-2 EUDAMED
Model / Reference
14-5604-01 EUDAMED

Identifiers

Primary DI / UDI-DI
07333066015613 EUDAMED
Basic UDI-DI
7333066BUDI0110LN EUDAMED
EMDN Code
W0102100199 AUTOIMMUNE CONNECTIVE TISSUE DISEASES TESTING - OTHER EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Sweden EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

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

New Device

No

EUDAMED

EliA Mi-2 Well 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Phadia AB
EUDAMED SRN
SE-MF-000014170

Sources (1)

  • EUDAMED 3d2073c0-64ef-497a-9b69-26493f8ea1cf 61 fields · synced Aug 2, 2026