Cranioplasty sheet - UK MHRA Medical Device Registration
Cranioplasty sheet is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 88417. The device is manufactured by Kinamed Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Medes 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
Cranioplasty sheet
Type
Class IIb
Date Registered
Sep 15, 2024
Last Updated
Apr 22, 2024
Name
Medes Ltd.Relationship Type
Address
5 Beaumont Gate, Shenley Hil
Radlett, Herts, England, United Kingdom
Postcode: WD77AR
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