United Kingdom MHRA device registration 182292

Cardiac/peripheral vascular guidewire, single-use

United Kingdom flagUnited Kingdom·General Medical Device·MaRVis Interventional GmbH·Registered Nov 26, 2024
Registration details
Device ID
182292
MHRA Reference Number
182292
Date Registered
Nov 26, 2024
Last Updated
Sep 11, 2024
Device classification
Device Type
General Medical Device
Devices
Cardiac/peripheral vascular guidewire, single-use
Type
Class IIa
Manufacturer
Address
Adlerstr. 9
Garmisch-Partenkirchen, Germany
Created Date
Nov 24, 2023
Authorized Representative
Relationship Type
UK Responsible Person
Address
6 Wilmslow Road, Rusholme
Manchester, England, United Kingdom
Postcode: M14 5TP
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About this record

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 182292. The device is manufactured by MaRVis Interventional GmbH from Germany, 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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