Clostridium difficile antigen IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Clostridium difficile antigen IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 123774. The device is manufactured by TECHLAB, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Emergo Consulting (UK) Limited .

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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Clostridium difficile antigen IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 123774•Ref: 123774

Device Type

In Vitro Diagnostic Device

Devices

Clostridium difficile antigen IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Aug 25, 2024

Last Updated

Apr 17, 2024

Manufacturer Information

Name

TECHLAB, Inc.

Address

2001 Kraft Drive

Blacksburg, Virgina, United States

Created Date

Dec 17, 2021

Authorized Representative

Name

Emergo Consulting (UK) Limited

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 – UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

DJ Fang

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Clostridium difficile antigen IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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