United Kingdom MHRA device registration 184976

Buffered sample diluent IVD

United Kingdom·In Vitro Diagnostic Device·Hologic, Inc.·Registered Nov 26, 2024

Registration details

Device ID: 184976
MHRA Reference Number: 184976
Date Registered: Nov 26, 2024
Last Updated: Jun 20, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Buffered sample diluent IVD
Type: Class A

Manufacturer

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

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About this record

Buffered sample diluent IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 184976. 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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