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 76093. The device is manufactured by Baylis Medical Company, Inc from Canada, classified as General Medical Device. The authorized representative in the UK is Adveniunt Medical International Limited (trading as Quality First International).

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: 76093•Ref: 76093

Device Type

General Medical Device

Devices

Cardiac/peripheral vascular guidewire, single-use

Type

Class III

Date Registered

Jan 31, 2020

Last Updated

Oct 13, 2022

Manufacturer Information

Name

Baylis Medical Company, Inc

Address

2645 Matheson Blvd

Ontario, East Mississauga, Canada

Created Date

Jan 31, 2020

Authorized Representative

Name

Adveniunt Medical International Limited (trading as Quality First International)

Relationship Type

UK Responsible Person

Address

1 Cooks Road Stratford

London, England, United Kingdom

Postcode: E15 2PW

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Other Products from Baylis Medical Company, Inc (10)

Other Products from Same Authorized Representative (10)

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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