Allergen-specific immunoglobulin E (IgE) antibody IVD, kit, rapid ICT, self-testing - UK MHRA Medical Device Registration

Allergen-specific immunoglobulin E (IgE) antibody IVD, kit, rapid ICT, self-testing is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 158732. The device is manufactured by PRIMA Lab SA from Switzerland, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK Ltd..

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In Vitro Diagnostic Device

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Allergen-specific immunoglobulin E (IgE) antibody IVD, kit, rapid ICT, self-testing

MHRA Device ID: 158732•Ref: 158732

Device Type

In Vitro Diagnostic Device

Devices

Allergen-specific immunoglobulin E (IgE) antibody IVD, kit, rapid ICT, self-testing

Type

IVD Devices for Self-Testing

Date Registered

Nov 26, 2024

Last Updated

May 22, 2024

Manufacturer Information

Name

PRIMA Lab SA

Address

Via Antonio Monti Balerna

Balerna, Mendrisio, Switzerland

Created Date

Jul 9, 2021

Authorized Representative

Name

Qarad UK Ltd.

Relationship Type

UK Responsible Person

Address

8 Northumberland Ave

Westminster, London , England, United Kingdom

Postcode: WC2N 5BY

DJ Fang

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Allergen-specific immunoglobulin E (IgE) antibody IVD, kit, rapid ICT, self-testing - UK MHRA Medical Device Registration

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