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

Mycoplasma pneumoniae 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 183301. The device is manufactured by Assure Tech. (Hangzhou) Co., Ltd., from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Medimap Ltd.

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Mycoplasma pneumoniae antigen IVD, kit, rapid ICT, clinical

MHRA Device ID: 183301•Ref: 183301

Device Type

In Vitro Diagnostic Device

Devices

Mycoplasma pneumoniae antigen IVD, kit, rapid ICT, clinical

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Mar 23, 2024

Manufacturer Information

Name

Assure Tech. (Hangzhou) Co., Ltd.,

Address

Building 4, No 1418-50 Moganshan Road Gongshu District

Zheijiang, Hangzhou, China

Created Date

May 12, 2022

Authorized Representative

Name

Medimap Ltd

Relationship Type

UK Responsible Person

Address

2 The Drift

Thurston, Suffolk, United Kingdom

Postcode: IP31 3RT

DJ Fang

MedTech Regulatory Expert

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

Device Type

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Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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