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 202885. The device is manufactured by Lake Region Medical from United States, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (UK) Limited .

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Cardiac/peripheral vascular guidewire, single-use

MHRA Device ID: 202885•Ref: 202885

Device Type

General Medical Device

Devices

Cardiac/peripheral vascular guidewire, single-use

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Apr 30, 2024

Manufacturer Information

Name

Lake Region Medical

Address

340 Lake Hazeltine Drive

Chaska, Minnesota, United States

Created Date

Apr 29, 2021

Authorized Representative

Name

Emergo Consulting (UK) Limited

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 – UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

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Other Products from Lake Region Medical (3)

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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