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 165386. The device is manufactured by BIOSYNEX SWISS SA from Switzerland, 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, kit, rapid ICT, clinical

MHRA Device ID: 165386•Ref: 165386

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

Sep 10, 2024

Manufacturer Information

Name

BIOSYNEX SWISS SA

Address

Rue De Rossemaison 100

Delemont, Switzerland

Created Date

Jun 24, 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

MedTech Regulatory Expert

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Other Products from BIOSYNEX SWISS SA (10)

Other Products from Same Authorized Representative (10)

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

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Address

DJ Fang

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