Dental implant suprastructure, temporary, preformed, single-use - UK MHRA Medical Device Registration
Dental implant suprastructure, temporary, preformed, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 158272. The device is manufactured by Zimmer Dental Inc from United States, classified as General Medical Device. The authorized representative in the UK is Biomet 3i 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
Dental implant suprastructure, temporary, preformed, single-use
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Sep 20, 2023
Address
1900 Aston Ave
Carlsbad, California, United States
Created Date
Oct 14, 2022
Name
Biomet 3i UK LtdRelationship Type
Address
1 Glass Wharf Burges Salmon Rep Office
Bristol, England, United Kingdom
Postcode: BS2 0ZX
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Dental implant suprastructure, permanent, preformed
Type: General Medical Device
Registered: Nov 26, 2024
Dental implant suprastructure, permanent, preformed
Type: General Medical Device
Registered: Nov 26, 2024
Dental implant suprastructure, permanent, preformed
Type: General Medical Device
Registered: Nov 26, 2024
Dental implant suprastructure, permanent, preformed
Type: General Medical Device
Registered: Nov 26, 2024
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Registered: Nov 26, 2024
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Manufacturer: Zfx GmbH
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Dental implant suprastructure, permanent, preformed
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Manufacturer: Zimmer Dental Inc

