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

Allergen-specific immunoglobulin E (IgE) antibody IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 179643. The device is manufactured by Koch Biotechnology (Beijing) Co., Ltd from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is PureUKCA Ltd.

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

MHRA Device ID: 179643•Ref: 179643

Device Type

In Vitro Diagnostic Device

Devices

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

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Jan 24, 2024

Manufacturer Information

Name

Koch Biotechnology (Beijing) Co., Ltd

Address

No.16, Chunlin street, Daxing District

Beijing, China

Created Date

Aug 24, 2022

Authorized Representative

Name

PureUKCA Ltd

Relationship Type

UK Responsible Person

Address

59 St. Martin's Lane

London, Middlesex, England, United Kingdom

Postcode: WC2N 4JS

DJ Fang

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

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