Treponema pallidum reagin antibody IVD, kit, agglutination - UK MHRA Medical Device Registration

Treponema pallidum reagin antibody IVD, kit, agglutination is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 190361. The device is manufactured by VeroTest Sdn Bhd Company from Malaysia, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Atlas Medical.

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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Treponema pallidum reagin antibody IVD, kit, agglutination

MHRA Device ID: 190361•Ref: 190361

Device Type

In Vitro Diagnostic Device

Devices

Treponema pallidum reagin antibody IVD, kit, agglutination

Type

IVD General

Date Registered

Nov 19, 2024

Last Updated

Apr 17, 2024

Manufacturer Information

Name

VeroTest Sdn Bhd Company

Address

Unit G-E-2A Enterprise 4,Technology Park Malaysia, 57000 Bukit Jalil, Kuala Lumpur, Malaysia

Kuala Lumpur, Malaysia

Created Date

Apr 3, 2024

Authorized Representative

Name

Atlas Medical

Relationship Type

UK Responsible Person

Address

William James House Cowley Road

Cambridge, United Kingdom

Postcode: CB4 0WX

DJ Fang

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Treponema pallidum reagin antibody IVD, kit, agglutination - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

DJ Fang

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