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 166746. The device is manufactured by JOTEC GmbH from Germany, classified as General Medical Device. The authorized representative in the UK is OMC MEDICAL 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: 166746•Ref: 166746

Device Type

General Medical Device

Devices

Cardiac/peripheral vascular guidewire, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Apr 16, 2024

Manufacturer Information

Name

JOTEC GmbH

Address

Lotzenacker 23

Hechingen, Germany

Created Date

Feb 20, 2023

Authorized Representative

Name

OMC MEDICAL Ltd

Relationship Type

UK Responsible Person

Address

Planet House North Heath Lane

Horsham, West Sussex, United Kingdom

Postcode: RH12 5QE

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Other Products from JOTEC GmbH (9)

Other Products from Same Authorized Representative (10)

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

Device Type

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Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

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