Mycoplasma pneumoniae total antibody IVD, reagent - UK MHRA Medical Device Registration

Mycoplasma pneumoniae total antibody IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 184483. The device is manufactured by Hangzhou Tongzhou Biotechnology Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is lotus global co 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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Mycoplasma pneumoniae total antibody IVD, reagent

MHRA Device ID: 184483•Ref: 184483

Device Type

In Vitro Diagnostic Device

Devices

Mycoplasma pneumoniae total antibody IVD, reagent

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Mar 12, 2024

Manufacturer Information

Name

Hangzhou Tongzhou Biotechnology Co., Ltd.

Address

Room 102, Building 4, No. 191, Xintian Road, Yunhe Street, Linping District

Hangzhou, Zhejiang, China

Created Date

Jan 11, 2024

Authorized Representative

Name

lotus global co ltd

Relationship Type

UK Responsible Person

Address

23 Maine Street

Reading, Reading, England, United Kingdom

Postcode: RG2 6AG

DJ Fang

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Mycoplasma pneumoniae total antibody IVD, reagent - UK MHRA Medical Device Registration

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Address

DJ Fang

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