Evacuated blood collection tube IVD, clot activator - UK MHRA Medical Device Registration

Evacuated blood collection tube IVD, clot activator is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 112256. The device is manufactured by Shenyang Bokan Biotechnology Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is SUNGO Certification Company Limited.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Evacuated blood collection tube IVD, clot activator

MHRA Device ID: 112256•Ref: 112256

Device Type

In Vitro Diagnostic Device

Devices

Evacuated blood collection tube IVD, clot activator

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Aug 15, 2024

Manufacturer Information

Name

Shenyang Bokan Biotechnology Co., Ltd.

Address

Gate 1, No. 33-22, Punan Road, Shenbei New District, Shenyang

Liaoning Province, China

Created Date

Nov 11, 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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Evacuated blood collection tube IVD, clot activator - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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