Patient positioning foam mould kit - UK MHRA Medical Device Registration
Patient positioning foam mould kit is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 185995. The device is manufactured by Klarity Medical Products, LLC from United States, classified as General Medical Device. The authorized representative in the UK is AJW Technology Consulting 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
Patient positioning foam mould kit
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Oct 9, 2024
Address
600 Industrial Parkway
Heath, United States
Created Date
Dec 22, 2023
Relationship Type
Address
4/4a Bloomsbury Square
London, England, United Kingdom
Postcode: WC1A 2RP
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