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 89509. The device is manufactured by Cardiovascular Systems, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is ICON (LR) 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: 89509•Ref: 89509

Device Type

General Medical Device

Devices

Cardiac/peripheral vascular guidewire, single-use

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Jul 18, 2024

Manufacturer Information

Name

Cardiovascular Systems, Inc.

Address

1225 Old Highway 8 NW

Saint Paul, Minnesota, United States

Created Date

Jul 19, 2021

Authorized Representative

Name

ICON (LR) Limited

Relationship Type

UK Responsible Person

Address

500 South Oak Way Green Park

Reading, England, United Kingdom

Postcode: RG2 6AD

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

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Address

Created Date

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