Patient lifting system stretcher - UK MHRA Medical Device Registration
Patient lifting system stretcher is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 103440. The device is manufactured by Handi-Move NV from Belgium, classified as General Medical Device. The authorized representative in the UK is Qarad UK 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 lifting system stretcher
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Aug 1, 2024
Name
Handi-Move NVAddress
Ten Beukeboom 13 Ambachtelijke Zone Appelterre
Ninove, Belgium
Created Date
Sep 9, 2021
Name
Qarad UK Ltd.Relationship Type
Address
8 Northumberland Ave
Westminster, London , England, United Kingdom
Postcode: WC2N 5BY
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