Gastro-urological guidewire, single-use - UK MHRA Medical Device Registration

Gastro-urological guidewire, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 188693. 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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Gastro-urological guidewire, single-use

MHRA Device ID: 188693•Ref: 188693

Device Type

General Medical Device

Devices

Gastro-urological guidewire, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Sep 10, 2024

Manufacturer Information

Name

PIOLAX MEDICAL DEVICES, INC.

Address

2265-3 Kamiyabe-cho, Totsuka-ku

Yokohama-shi, Kanagawa , Japan

Created Date

Aug 31, 2021

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

DJ Fang

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Other Products from PIOLAX MEDICAL DEVICES, INC. (3)

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Gastro-urological guidewire, single-use - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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