Peripheral vascular guidewire extension - UK MHRA Medical Device Registration
Peripheral vascular guidewire extension is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 193318. 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.
Device Type
General Medical Device
Devices
Peripheral vascular guidewire extension
Type
Class III
Date Registered
Nov 26, 2024
Last Updated
May 21, 2024
Name
phenox GmbHAddress
Lise-Meitner-Allee 31
Bochum, North Rhine Westphalia , Germany
Created Date
May 15, 2024
Relationship Type
Address
Compass House, Vision Park Histon c/o Cr360 โ UL International
Cambridge, England, United Kingdom
Postcode: CB24 9BZ
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