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 196192. The device is manufactured by Opsens, Inc. from Canada, classified as General Medical Device. The authorized representative in the UK is MDSS-UK RP 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: 196192•Ref: 196192

Device Type

General Medical Device

Devices

Cardiac/peripheral vascular guidewire, single-use

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Jan 25, 2024

Manufacturer Information

Name

Opsens, Inc.

Address

750 boul. du Parc Technologique

Quebec, QC, Canada

Created Date

Apr 22, 2021

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

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Other Products from Opsens, Inc. (3)

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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

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