Endoscopic overtube, single-use - UK MHRA Medical Device Registration

Endoscopic overtube, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 155850. The device is manufactured by H&A Mui Enterprises Inc (Mui Scientific) from Canada, classified as General Medical Device. The authorized representative in the UK is Advena Ltd.

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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Endoscopic overtube, single-use

MHRA Device ID: 155850•Ref: 155850

Device Type

General Medical Device

Devices

Endoscopic overtube, single-use

Type

Class IIa

Date Registered

Sep 8, 2022

Last Updated

Feb 10, 2023

Manufacturer Information

Name

H&A Mui Enterprises Inc (Mui Scientific)

Address

Unit 34 145 Traders Blvd. E,

Mississauga, Ontario, Canada

Created Date

Sep 8, 2022

Authorized Representative

Name

Advena Ltd

Relationship Type

UK Responsible Person

Address

Pure Offices Plato Close

Warwick, England, United Kingdom

Postcode: CV34 6WE

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Other Products from H&A Mui Enterprises Inc (Mui Scientific) (6)

Other Products from Same Authorized Representative (10)

Endoscopic overtube, 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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