United Kingdom MHRA device registration 90734

General specimen container IVD, additive/medium

United Kingdom·In Vitro Diagnostic Device·Hangzhou Lifereal Biotechnology Co., Ltd.·Registered Nov 26, 2024

Registration details

Device ID: 90734
MHRA Reference Number: 90734
Date Registered: Nov 26, 2024
Last Updated: Jun 26, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: General specimen container IVD, additive/medium
Type: IVD General

Manufacturer

Name: Hangzhou Lifereal Biotechnology Co., Ltd.
Address: 1st & 2nd Floor of Building 4 and 1st Floor of Building 3, No 21 Futai Road Zhongtai Street, Yuhang District
Hangzhou, China
Created Date: Jul 27, 2021

Authorized Representative

Name: SUNGO Certification Company Limited
Relationship Type: UK Responsible Person
Address: 3rd Floor, 70 Gracechurch Street
London, England, United Kingdom
Postcode: EC3V 0HR

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About this record

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 90734. The device is manufactured by Hangzhou Lifereal Biotechnology Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is SUNGO Certification Company Limited.

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