Treponema pallidum immunoglobulin G (IgG)/IgM antibody IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

Treponema pallidum immunoglobulin G (IgG)/IgM antibody IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 197525. The device is manufactured by VivaChek Biotech (Hangzhou) 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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In Vitro Diagnostic Device

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Treponema pallidum immunoglobulin G (IgG)/IgM antibody IVD, kit, rapid ICT, clinical

MHRA Device ID: 197525•Ref: 197525

Device Type

In Vitro Diagnostic Device

Devices

Treponema pallidum immunoglobulin G (IgG)/IgM antibody IVD, kit, rapid ICT, clinical

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Jun 11, 2024

Manufacturer Information

Name

VivaChek Biotech (Hangzhou) Co., Ltd.

Address

Level 2, Block 2, 146 East Chaofeng Rd., Yuhang Economy Development Zone,

Hangzhou, Zhejiang, China

Created Date

Mar 14, 2021

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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Other Products from VivaChek Biotech (Hangzhou) Co., Ltd. (10)

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Treponema pallidum immunoglobulin G (IgG)/IgM antibody IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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