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EliA CTD Screen Well

EUDAMED

Class B (EU MDR)

Ref 14-5596-01

by Phadia AB

Identity

Trade Name
EliA CTD Screen Well EUDAMED
Device Name
EliA CTD Screen EUDAMED
Model / Reference
14-5596-01 EUDAMED

Identifiers

Primary DI / UDI-DI
07333066015569 EUDAMED
Basic UDI-DI
7333066BUDI0103LR EUDAMED
EMDN Code
W0102100101 ANA SCREENING 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 CTD Screen 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

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Manufacturer

Manufacturer
Phadia AB
EUDAMED SRN
SE-MF-000014170

Sources (1)

  • EUDAMED 18743221-e7ec-4066-9eaf-f2b099303286 61 fields · synced Jun 18, 2026