Bone matrix implant, synthetic, non-antimicrobial - UK MHRA Medical Device Registration
Bone matrix implant, synthetic, non-antimicrobial is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 77852. The device is manufactured by TEKNIMED SAS from France, classified as General Medical Device. The authorized representative in the UK is Advena 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 matrix implant, synthetic, non-antimicrobial
Type
Class III
Date Registered
Apr 29, 2021
Last Updated
Jan 6, 2024
Name
Advena LtdRelationship Type
Address
Pure Offices Plato Close
Warwick, England, United Kingdom
Postcode: CV34 6WE
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