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 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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Cardiac/peripheral vascular guidewire, single-use

MHRA Device ID: 182292•Ref: 182292

Device Type

General Medical Device

Devices

Cardiac/peripheral vascular guidewire, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Sep 11, 2024

Manufacturer Information

Name

MaRVis Interventional GmbH

Address

Adlerstr. 9

Garmisch-Partenkirchen, Germany

Created Date

Nov 24, 2023

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

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

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