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 95816. The device is manufactured by Meridian Bioscience Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Launch Diagnostics Limited.

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

MHRA Device ID: 95816•Ref: 95816

Device Type

In Vitro Diagnostic Device

Devices

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

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Sep 10, 2024

Manufacturer Information

Name

Meridian Bioscience Inc.

Address

3471 River Hills Drive

Cincinnati, OH, United States

Created Date

Aug 18, 2021

Authorized Representative

Name

Launch Diagnostics Limited

Relationship Type

UK Responsible Person

Address

Unit 20 Ash Way Thorp Arch Estate

Wetherby, England, United Kingdom

Postcode: LS23 7FA

DJ Fang

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

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