Rotavirus antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

Rotavirus antigen IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 95821. 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.

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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Rotavirus antigen IVD, kit, rapid ICT, clinical

MHRA Device ID: 95821•Ref: 95821

Device Type

In Vitro Diagnostic Device

Devices

Rotavirus antigen IVD, kit, rapid ICT, clinical

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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Rotavirus antigen IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

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