Sexually transmitted infection (STI) testing specimen collection kit IVD, clinical - UK MHRA Medical Device Registration

Sexually transmitted infection (STI) testing specimen collection kit IVD, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 46162. The device is manufactured by Hologic, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Hologic Ltd..

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Sexually transmitted infection (STI) testing specimen collection kit IVD, clinical

MHRA Device ID: 46162•Ref: 46162

Device Type

In Vitro Diagnostic Device

Devices

Sexually transmitted infection (STI) testing specimen collection kit IVD, clinical

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Jun 20, 2024

Manufacturer Information

Name

Hologic, Inc.

Address

10210 Genetic Center Drive

San Diego, CA, United States

Created Date

Nov 6, 2017

Authorized Representative

Name

Hologic Ltd.

Relationship Type

UK Responsible Person

Address

Heron House 6 The Oaks Business Park Crewe Road Wythenshawe

Manchester, Lancashire, England, United Kingdom

Postcode: M23 9HZ

DJ Fang

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Sexually transmitted infection (STI) testing specimen collection kit IVD, clinical - UK MHRA Medical Device Registration

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