Pressure bandage, non-latex, single-use - UK MHRA Medical Device Registration
Pressure bandage, non-latex, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 172212. The device is manufactured by Orkla Wound Care AB from Sweden, classified as General Medical Device. The authorized representative in the UK is QAdvis 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
Pressure bandage, non-latex, single-use
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Feb 20, 2024
Name
QAdvis UK LtdRelationship Type
Address
55-66 Frederick Street
Edinburgh, EH2 1LS, Scotland, United Kingdom
Postcode: EH2 1LS
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