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

Legionella pneumophila 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 94110. The device is manufactured by Hangzhou Alltest Biotech Co Ltd from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Medimap Ltd.

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Legionella pneumophila antigen IVD, kit, rapid ICT, clinical

MHRA Device ID: 94110•Ref: 94110

Device Type

In Vitro Diagnostic Device

Devices

Legionella pneumophila antigen IVD, kit, rapid ICT, clinical

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Jun 15, 2024

Manufacturer Information

Name

Hangzhou Alltest Biotech Co Ltd

Address

#550 Yinhai Street Hangzhou Economic & Technological Development Area

Hangzhou, China

Created Date

Mar 9, 2021

Authorized Representative

Name

Medimap Ltd

Relationship Type

UK Responsible Person

Address

2 The Drift

Thurston, Suffolk, United Kingdom

Postcode: IP31 3RT

DJ Fang

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

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Date Registered

Last Updated

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Address

DJ Fang

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