Endoscopic antifog solution - UK MHRA Medical Device Registration
Endoscopic antifog solution is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 134591. The device is manufactured by DeRoyal Industries, Inc. 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
Endoscopic antifog solution
Type
Class I
Date Registered
Sep 27, 2021
Last Updated
Dec 22, 2022
Address
200 DeBusk Lane
Powell, Tennessee, United States
Created Date
Sep 27, 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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