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ImmunoCAP Allergen e4, Cow dander

EUDAMEDFDA UDI

Class B (EU MDR)

Ref 14-4166-01

by Phadia AB

Identity

Trade Name
ImmunoCAP Allergen e4, Cow dander EUDAMEDFDA UDI
Generic Name
Allergen-specific immunoglobulin E (IgE) antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI
Device Name
ImmunoCAP Allergen EUDAMED
ImmunoCAP Allergen e4, Cow dander FDA UDI
Model / Reference
14-4166-01 EUDAMEDFDA UDI
Description
ImmunoCAP Allergen e4, Cow dander FDA UDI

Identifiers

Catalog Number
14-4166-01 FDA UDI
Primary DI / UDI-DI
07333066001654 EUDAMEDFDA UDI
Basic UDI-DI
7333066BUDI0019M3 EUDAMED
510(k) Number
K051218 FDA UDI
FDA Product Code
DHB FDA UDI
EMDN Code
W01020202 IMMUNOGLOBULIN E - SPECIFIC, MONOTEST/MONORESULT EUDAMED
GMDN Term
Allergen-specific immunoglobulin E (IgE) antibody IVD, kit, enzyme immunoassay (EIA) FDA UDI

Classification

Device Class
Class B EUDAMED
Class II FDA UDI
Regulation Number
866.5750 FDA UDI
Market of Registration
Sweden EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

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

ImmunoCAP Allergen e4, Cow dander by Phadia AB — Class B — IVDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/IVDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Phadia AB
EUDAMED SRN
SE-MF-000014170

Sources (2)

  • EUDAMED 7f7b4e75-7fca-4853-a1d4-b3409265d473 61 fields · synced Jul 27, 2026
  • FDA UDI 02685dc7-c8e0-4299-8a4a-fd5aa3e4a4b9 37 fields · synced May 30, 2026