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 172829. The device is manufactured by Acon Laboratories, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MDSS-UK RP LIMITED.

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

MHRA Device ID: 172829•Ref: 172829

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

Mar 12, 2024

Manufacturer Information

Name

Acon Laboratories, Inc.

Address

5850 Oberlin Drive, #340

San Diego, CA, United States

Created Date

Mar 31, 2021

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

DJ Fang

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

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