Peripheral vascular guidewire, manual - UK MHRA Medical Device Registration

Peripheral vascular guidewire, manual is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 193317. The device is manufactured by phenox GmbH from Germany, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (UK) 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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Peripheral vascular guidewire, manual

MHRA Device ID: 193317•Ref: 193317

Device Type

General Medical Device

Devices

Peripheral vascular guidewire, manual

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

May 21, 2024

Manufacturer Information

Name

phenox GmbH

Address

Lise-Meitner-Allee 31

Bochum, North Rhine Westphalia , Germany

Created Date

May 15, 2024

Authorized Representative

Name

Emergo Consulting (UK) Limited

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 – UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

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Peripheral vascular guidewire, manual - UK MHRA Medical Device Registration

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