Eye pad - UK MHRA Medical Device Registration
Eye pad is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 112202. The device is manufactured by Maxtec, LLC from United States, 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.
Device Type
General Medical Device
Devices
Eye pad
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Nov 9, 2024
Name
Maxtec, LLCAddress
2305 South 1070 West
Salt Lake City, UT, United States
Created Date
Oct 15, 2021
Relationship Type
Address
Compass House, Vision Park Histon c/o Cr360 โ UL International
Cambridge, England, United Kingdom
Postcode: CB24 9BZ
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