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ImmunoCAP ISAC E Detection Antibody

EUDAMED

Class C (EU MDR)

Ref 81-1022-01

by Phadia AB

Identity

Trade Name
ImmunoCAP ISAC E Detection Antibody EUDAMED
Device Name
ImmunoCAP ISAC E112i EUDAMED
Model / Reference
81-1022-01 EUDAMED

Identifiers

Primary DI / UDI-DI
07333066021157 EUDAMED
Basic UDI-DI
7333066BUDI0036M3 EUDAMED
EMDN Code
W01020204 IMMUNOGLOBULIN E - MONOTEST/PLURIRESULT-MULTI AG EUDAMED

Classification

Device Class
Class C 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

ImmunoCAP ISAC E Detection Antibody by Phadia AB — Class C — 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 8a2629fc-139f-4c32-840c-c77442536941 61 fields · synced Jun 18, 2026