United Kingdom MHRA device registration 48251

Tissue specimen x-ray system IVD

United Kingdom flagUnited Kingdom·General Medical Device·Hologic, Inc.·Registered Aug 18, 2024
Registration details
Device ID
48251
MHRA Reference Number
48251
Date Registered
Aug 18, 2024
Last Updated
Mar 5, 2024
Device classification
Device Type
General Medical Device
Devices
Tissue specimen x-ray system IVD
Type
Class I
Manufacturer
Address
36 Apple Ridge Road
Danbury, Connecticut, United States
Created Date
Apr 4, 2019
Authorized Representative
Relationship Type
UK Responsible Person
Address
Heron House 6 The Oaks Business Park Crewe Road Wythenshawe
Manchester, Lancashire, England, United Kingdom
Postcode: M23 9HZ
Similar products

Devices with a matching generic name or device type registered with MHRA

Other products from Hologic, Inc.

Additional devices registered by the same manufacturer

Other products from same authorized representative

Additional devices represented by Hologic Ltd. in the UK

Cytomegalovirus (CMV) nucleic acid IVD, reagentNov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: Hologic, Inc.
Device ID: 86498
Cytomegalovirus (CMV) nucleic acid IVD, controlNov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: Hologic, Inc.
Device ID: 194420
Beta-haemolytic Group B Streptococcus nucleic acid IVD, kit, nucleic acid technique (NAT)Nov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: Hologic, Inc.
Device ID: 184966
Cytomegalovirus (CMV) nucleic acid IVD, kit, nucleic acid technique (NAT)Nov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: Hologic, Inc.
Device ID: 194418
Buffered sample diluent IVD, automated/semi-automated systemNov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: Hologic, Inc.
Device ID: 46161
Chlamydia trachomatis nucleic acid IVD, kit, nucleic acid technique (NAT)Nov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: Hologic, Inc.
Device ID: 194422
Beta-haemolytic Group B Streptococcus nucleic acid IVD, controlNov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: Hologic, Inc.
Device ID: 111374
Beta-haemolytic Group B Streptococcus nucleic acid IVD, controlNov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: Hologic, Inc.
Device ID: 184967
Beta-haemolytic Group B Streptococcus nucleic acid IVD, kit, nucleic acid technique (NAT)Nov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: Hologic, Inc.
Device ID: 111373
Fibronectin IVD, kit, enzyme immunohistochemistryNov 26, 2024
Type: In Vitro Diagnostic Device
Manufacturer: Hologic, Inc.
Device ID: 111920
About this record

Tissue specimen x-ray system IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 48251. The device is manufactured by Hologic, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Hologic Ltd..

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

Free DatabasePowered by Pure Global AIMHRA RegisteredGeneral Medical Device