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 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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General specimen container IVD, additive/medium

MHRA Device ID: 90734•Ref: 90734

Device Type

In Vitro Diagnostic Device

Devices

General specimen container IVD, additive/medium

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Jun 26, 2024

Manufacturer Information

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

DJ Fang

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Other Products from Hangzhou Lifereal Biotechnology Co., Ltd. (1)

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Type: In Vitro Diagnostic Device

Registered: Nov 26, 2024

Other Products from Same Authorized Representative (10)

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

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