General specimen container IVD, additive/medium - UK MHRA Medical Device Registration

General specimen container IVD, additive/medium is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 165207. 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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General specimen container IVD, additive/medium

MHRA Device ID: 165207•Ref: 165207

Device Type

In Vitro Diagnostic Device

Devices

General specimen container IVD, additive/medium

Type

Class A

Date Registered

Apr 11, 2024

Last Updated

Mar 12, 2024

Manufacturer Information

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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General specimen container IVD, additive/medium - UK MHRA Medical Device Registration

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