Nucleic acid amplification mastermix reagent IVD - UK MHRA Medical Device Registration

Nucleic acid amplification mastermix reagent IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 178346. The device is manufactured by GeneProof a.s. from Czechia, classified as In Vitro Diagnostic Device. The authorized representative in the UK is confinis (UK) RP 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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Nucleic acid amplification mastermix reagent IVD

MHRA Device ID: 178346•Ref: 178346

Device Type

In Vitro Diagnostic Device

Devices

Nucleic acid amplification mastermix reagent IVD

Type

IVD General

Date Registered

Feb 23, 2024

Last Updated

Sep 16, 2023

Manufacturer Information

Name

GeneProof a.s.

Address

Videnska 101/119

Brno, Dolni-Herspice, Czechia

Created Date

Sep 4, 2023

Authorized Representative

Name

confinis (UK) RP Ltd

Relationship Type

UK Responsible Person

Address

St John's Innovation Centre Cowley Road

Cambridge, England, United Kingdom

Postcode: CB4 0WS

DJ Fang

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Nucleic acid amplification mastermix reagent IVD - UK MHRA Medical Device Registration

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