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 165250. The device is manufactured by SP Medical A/S from Denmark, classified as General Medical Device. The authorized representative in the UK is Advena Ltd.

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: 165250•Ref: 165250

Device Type

General Medical Device

Devices

Cardiac/peripheral vascular guidewire, single-use

Type

Class III

Date Registered

Sep 29, 2024

Last Updated

Aug 10, 2024

Manufacturer Information

Name

SP Medical A/S

Address

Møllevej 1

Karise, Denmark

Created Date

Aug 25, 2021

Authorized Representative

Name

Advena Ltd

Relationship Type

UK Responsible Person

Address

Pure Offices Plato Close

Warwick, England, United Kingdom

Postcode: CV34 6WE

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Other Products from SP Medical A/S (2)

Gastro-urological guidewire, single-use

Type: General Medical Device

Registered: Sep 29, 2024

Peripheral vascular guidewire, manual

Type: General Medical Device

Registered: Sep 29, 2024

Other Products from Same Authorized Representative (10)

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

Device Type

Devices

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Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

DJ Fang

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