Bone access cannula - UK MHRA Medical Device Registration
Bone access cannula is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 80023. The device is manufactured by MEDOS INTERNATIONAL SARL from Switzerland, classified as General Medical Device. The authorized representative in the UK is Johnson & Johnson Medical 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
Bone access cannula
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
May 15, 2024
Relationship Type
Address
Baird House 4 Lower Gilmore Bank
Edinburgh, Scotland, United Kingdom
Postcode: EH3 9QP
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