Cavity-wound management dressing, non-antimicrobial - UK MHRA Medical Device Registration
Cavity-wound management dressing, non-antimicrobial is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 96513. The device is manufactured by Ferris Mfg. Corp. 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
Cavity-wound management dressing, non-antimicrobial
Type
Class IIb
Date Registered
Nov 26, 2024
Last Updated
Jul 11, 2024
Address
5133 Northeast Parkway
Forth Worth, Texas, United States
Created Date
Aug 19, 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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