United Kingdom MHRA device registration 70155

Buffered sample diluent IVD, automated/semi-automated system

United Kingdom·In Vitro Diagnostic Device·Tosoh Europe·Registered Nov 26, 2024

Registration details

Device ID: 70155
MHRA Reference Number: 70155
Date Registered: Nov 26, 2024
Last Updated: Jan 18, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Buffered sample diluent IVD, automated/semi-automated system
Type: IVD General

Manufacturer

Name: Tosoh Europe
Address: Transportstraat 4
Tessenderlo, Belgium
Created Date: Mar 23, 2021

Authorized Representative

Name: Tosoh Bioscience Limited
Relationship Type: UK Responsible Person
Address: Lytchett House Wareham Road 13 Freeland Park
Poole, Dorset, England, United Kingdom
Postcode: BH16 6FA

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About this record

Buffered sample diluent IVD, automated/semi-automated system is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 70155. The device is manufactured by Tosoh Europe from Belgium, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Tosoh Bioscience Limited.

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