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 71669. The device is manufactured by SentreHEART from United States, classified as General Medical Device. The authorized representative in the UK is AtriCure UK 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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Cardiac/peripheral vascular guidewire, single-use

MHRA Device ID: 71669•Ref: 71669

Device Type

General Medical Device

Devices

Cardiac/peripheral vascular guidewire, single-use

Type

Class III

Date Registered

Apr 1, 2021

Last Updated

Nov 23, 2023

Manufacturer Information

Name

SentreHEART

Address

300 Saginaw Drive

Redwood City, California, United States

Created Date

Apr 1, 2021

Authorized Representative

Name

AtriCure UK limited

Relationship Type

UK Responsible Person

Address

1 Princeton Mews 167-169 London Road

Kingston Upon Thames , Surrey, England, United Kingdom

Postcode: KT2 6PT

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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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Cardiac/peripheral vascular guidewire, single-use

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