Urea IVD, reagent - UK MHRA Medical Device Registration

Urea IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 160389. The device is manufactured by Zhejiang PushKang 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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Urea IVD, reagent

MHRA Device ID: 160389•Ref: 160389

Device Type

In Vitro Diagnostic Device

Devices

Urea IVD, reagent

Type

IVD General

Date Registered

Oct 29, 2024

Last Updated

Oct 8, 2023

Manufacturer Information

Name

Zhejiang PushKang Biotechnology Co., Ltd.

Address

C408, Science and Technology Innovation Park No. 398, Mahuan Road, Binhai New Area, Shaoxing

Zhejiang Province, China

Created Date

Nov 11, 2022

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 Zhejiang PushKang Biotechnology Co., Ltd. (10)

Other Products from Same Authorized Representative (10)

Urea IVD, reagent - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

DJ Fang

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