United Kingdom MHRA device registration 165203

Multiple-type gastrointestinal pathogen nucleic acid IVD, calibrator

United Kingdom·In Vitro Diagnostic Device·Mobidiag Oy·Registered Apr 11, 2024

Registration details

Device ID: 165203
MHRA Reference Number: 165203
Date Registered: Apr 11, 2024
Last Updated: Mar 12, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Multiple-type gastrointestinal pathogen nucleic acid IVD, calibrator
Type: IVD General

Manufacturer

Name: Mobidiag Oy
Address: Keilaranta 16A
Espoo, Finland
Created Date: Jan 20, 2023

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

Multiple-type gastrointestinal pathogen nucleic acid IVD, calibrator is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 165203. The device is manufactured by Mobidiag Oy from Finland, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Hologic Ltd..

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