United Kingdom MHRA device registration 179643

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

United Kingdom·In Vitro Diagnostic Device·Koch Biotechnology (Beijing) Co., Ltd ·Registered Nov 26, 2024

Registration details

Device ID: 179643
MHRA Reference Number: 179643
Date Registered: Nov 26, 2024
Last Updated: Jan 24, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Allergen-specific immunoglobulin E (IgE) antibody IVD, kit, rapid ICT, clinical
Type: IVD General

Manufacturer

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

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About this record

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.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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