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 72034. The device is manufactured by Medtronic, Inc from United States, classified as Active Implantable Device. The authorized representative in the UK is Medtronic Limited.

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Cardiac/peripheral vascular guidewire, single-use

MHRA Device ID: 72034•Ref: 72034

Device Type

Active Implantable Device

Devices

Cardiac/peripheral vascular guidewire, single-use

Date Registered

Nov 26, 2024

Last Updated

Dec 16, 2023

Manufacturer Information

Name

Medtronic, Inc

Address

710 Medtronic Parkway

Minneapolis, MN, United States

Created Date

Feb 2, 2021

Authorized Representative

Name

Medtronic Limited

Relationship Type

UK Responsible Person

Address

Building 9 Croxley Park

Watford, Herts, England, United Kingdom

Postcode: WD18 8WW

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Other Products from Medtronic, Inc (10)

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

Device Type

Devices

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

Cardiac/peripheral vascular guidewire, single-use

Cardiac/peripheral vascular guidewire, single-use

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