United Kingdom MHRA device registration 173521

Faecal occult blood IVD, kit, rapid ICT, clinical

United Kingdom·In Vitro Diagnostic Device·Hangzhou Alltest Biotech Co Ltd·Registered Nov 26, 2024

Registration details

Device ID: 173521
MHRA Reference Number: 173521
Date Registered: Nov 26, 2024
Last Updated: Jun 15, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Faecal occult blood IVD, kit, rapid ICT, clinical
Type: IVD General

Manufacturer

Name: Hangzhou Alltest Biotech Co Ltd
Address: #550 Yinhai Street Hangzhou Economic & Technological Development Area
Hangzhou, China
Created Date: Mar 9, 2021

Authorized Representative

Name: Medimap Ltd
Relationship Type: UK Responsible Person
Address: 2 The Drift
Thurston, Suffolk, United Kingdom
Postcode: IP31 3RT

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About this record

Faecal occult blood IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 173521. The device is manufactured by Hangzhou Alltest Biotech Co Ltd from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Medimap Ltd.

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