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.
Device Type
General Medical Device
Devices
Endoscopic overtube, single-use
Type
Class IIa
Date Registered
Sep 8, 2022
Last Updated
Feb 10, 2023
Address
Unit 34 145 Traders Blvd. E,
Mississauga, Ontario, Canada
Created Date
Sep 8, 2022
Name
Advena LtdRelationship Type
Address
Pure Offices Plato Close
Warwick, England, United Kingdom
Postcode: CV34 6WE
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