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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 130049. The device is manufactured by Arlington Scientific, Inc from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Werfen Ltd.

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In Vitro Diagnostic Device
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Treponema pallidum reagin antibody IVD, kit, agglutination
MHRA Device ID: 130049โ€ขRef: 130049

Device Type

In Vitro Diagnostic Device

Devices

Treponema pallidum reagin antibody IVD, kit, agglutination

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Aug 21, 2024

Manufacturer Information

Address

1840 North Technology Drive Springville

Utah, United States

Created Date

Dec 30, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

712 The Quadrant, Cavendish Avenue, Birchwood, Warrington WA3 6DE Manchester

Manchester, England, United Kingdom

Postcode: WA3 6DE

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