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Multiple Bordetella species antibody IVD, reagent - UK MHRA Medical Device Registration

Multiple Bordetella species antibody IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 184379. The device is manufactured by TestLine Clinical Diagnostics s.r.o from Czechia, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Oxford Biosystems 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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Multiple Bordetella species antibody IVD, reagent
MHRA Device ID: 184379โ€ขRef: 184379

Device Type

In Vitro Diagnostic Device

Devices

Multiple Bordetella species antibody IVD, reagent

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Nov 12, 2024

Manufacturer Information

Address

Kล™iลพรญkova 188/68

Brno, Czechia

Created Date

Nov 24, 2022

Authorized Representative

Relationship Type

UK Responsible Person

Address

184B Park Drive Milton Park Abingdon

Abingdon, Oxfordshire, United Kingdom

Postcode: OX14 4SE

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