Treponema pallidum total antibody IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

Treponema pallidum total 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 92418. The device is manufactured by Abbott Diagnostics Medical Co., Ltd. from Japan, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Unipath Limited (trading as Alere International).

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Treponema pallidum total antibody IVD, kit, rapid ICT, clinical

MHRA Device ID: 92418•Ref: 92418

Device Type

In Vitro Diagnostic Device

Devices

Treponema pallidum total antibody IVD, kit, rapid ICT, clinical

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Nov 15, 2024

Manufacturer Information

Name

Abbott Diagnostics Medical Co., Ltd.

Address

357 Matsuhidai Matsudo-shi

Chiba, Japan

Created Date

Apr 18, 2021

Authorized Representative

Name

Unipath Limited (trading as Alere International)

Relationship Type

UK Responsible Person

Address

Abbott House Vanwall Road Vanwall Business Park

Maidenhead, Windsor And Maidenhead, England, United Kingdom

Postcode: SL6 4XE

DJ Fang

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Treponema pallidum total antibody IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

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