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 177766. The device is manufactured by AtriCure, Inc. 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: 177766•Ref: 177766

Device Type

General Medical Device

Devices

Cardiac/peripheral vascular guidewire, single-use

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Apr 20, 2024

Manufacturer Information

Name

AtriCure, Inc.

Address

7555 Innovation Way

Mason, Ohio, United States

Created Date

Mar 5, 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

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Date Registered

Last Updated

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Created Date

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Address

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