Cardiac/peripheral vascular guidewire, single-use - UK MHRA Medical Device Registration

Cardiac/peripheral vascular guidewire, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 92697. The device is manufactured by Guangdong Baihe Medical Technology Co., Ltd from China, classified as General Medical Device. The authorized representative in the UK is CMC Medical Devices 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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Cardiac/peripheral vascular guidewire, single-use

MHRA Device ID: 92697•Ref: 92697

Device Type

General Medical Device

Devices

Cardiac/peripheral vascular guidewire, single-use

Type

Class IIa

Date Registered

Jun 3, 2024

Last Updated

Oct 4, 2023

Manufacturer Information

Name

Guangdong Baihe Medical Technology Co., Ltd

Address

No.89, Taoyuan East Road, Nanhai, Foshan, Guangdong Province, P.R. China

Fo Shan, China

Created Date

Aug 6, 2021

Authorized Representative

Name

CMC Medical Devices LTD

Relationship Type

UK Responsible Person

Address

Office 32 19-21 Crawford Street

London, United Kingdom

Postcode: W1H 1PJ

DJ Fang

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Other Products from Guangdong Baihe Medical Technology Co., Ltd (10)

Other Products from Same Authorized Representative (10)

Cardiac/peripheral vascular guidewire, single-use - 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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