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

Evacuated blood collection tube IVD, clot activator/separator is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 204525. The device is manufactured by Guangzhou Improve Medical Instruments Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Umedwings UK LTD.

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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In Vitro Diagnostic Device
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Evacuated blood collection tube IVD, clot activator/separator
MHRA Device ID: 204525โ€ขRef: 204525

Device Type

In Vitro Diagnostic Device

Devices

Evacuated blood collection tube IVD, clot activator/separator

Type

Class A

Date Registered

Nov 26, 2024

Last Updated

Jun 4, 2024

Manufacturer Information

Address

No. 102, Kaiyuan Avenue, Science City Guangzhou Economic & Technological Development District

Guangzhou, Guangdong, China

Created Date

Apr 27, 2024

Authorized Representative

Relationship Type

UK Responsible Person

Address

291 Brighton Road

South Croydon, England, United Kingdom

Postcode: CR2 6EQ

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