Treponema pallidum immunoglobulin G (IgG)/IgM antibody IVD, control - UK MHRA Medical Device Registration

Treponema pallidum immunoglobulin G (IgG)/IgM antibody IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 72942. The device is manufactured by bioLytical Laboratories Inc. from Canada, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK Ltd..

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Treponema pallidum immunoglobulin G (IgG)/IgM antibody IVD, control

MHRA Device ID: 72942•Ref: 72942

Device Type

In Vitro Diagnostic Device

Devices

Treponema pallidum immunoglobulin G (IgG)/IgM antibody IVD, control

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

May 9, 2024

Manufacturer Information

Name

bioLytical Laboratories Inc.

Address

406-13251 Delf Place

Richmond, British Columbia, Canada

Created Date

Apr 13, 2021

Authorized Representative

Name

Qarad UK Ltd.

Relationship Type

UK Responsible Person

Address

8 Northumberland Ave

Westminster, London , England, United Kingdom

Postcode: WC2N 5BY

DJ Fang

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Other Products from bioLytical Laboratories Inc. (7)

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Treponema pallidum immunoglobulin G (IgG)/IgM antibody IVD, control - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Address

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Name

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DJ Fang

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