United Kingdom MHRA device registration 101794

Peripheral vascular guidewire, manual

United Kingdom flagUnited Kingdom·General Medical Device·PIOLAX MEDICAL DEVICES, INC.·Registered Oct 9, 2024
Registration details
Device ID
101794
MHRA Reference Number
101794
Date Registered
Oct 9, 2024
Last Updated
Sep 10, 2024
Device classification
Device Type
General Medical Device
Devices
Peripheral vascular guidewire, manual
Type
Class IIa
Manufacturer
Address
2265-3 Kamiyabe-cho, Totsuka-ku
Yokohama-shi, Kanagawa , Japan
Created Date
Aug 31, 2021
Authorized Representative
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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About this record

Peripheral vascular guidewire, manual is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 101794. The device is manufactured by PIOLAX MEDICAL DEVICES, INC. from Japan, 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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