Tourniquet cuff, single-use - UK MHRA Medical Device Registration
Tourniquet cuff, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 175001. The device is manufactured by Delfi Medical Innovations Inc from Canada, classified as General Medical Device. The authorized representative in the UK is International Associates 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
Tourniquet cuff, single-use
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Sep 3, 2024
Address
106 - 1099 West 8th Avenue
Vancouver, Canada
Created Date
Nov 17, 2021
Relationship Type
Address
38 Queen Street
Glasgow, Scotland, United Kingdom
Postcode: G1 3DX
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