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ImmunoCAP Allergen

EUDAMED

Class B (EU MDR)

Ref 14-5193-01

by Phadia AB

Identity

Device Name
ImmunoCAP Allergen EUDAMED
Model / Reference
14-5193-01 EUDAMED

Identifiers

Primary DI / UDI-DI
07333066008110 EUDAMED
Basic UDI-DI
7333066BUDI0017LX EUDAMED
EMDN Code
W01020202 IMMUNOGLOBULIN E - SPECIFIC, MONOTEST/MONORESULT EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Sweden EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

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

Category: Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent

ImmunoCAP Allergen by Phadia AB — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Allergen-specific immunoglobulin E (IgE) antibody IVD, reagent.

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 639b3abb-63d0-44cd-8385-f1ecfb1c95a7 61 fields · synced May 23, 2026