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 175795. The device is manufactured by New Ancorvis Srl from Italy, classified as General Medical Device. The authorized representative in the UK is Donawa Lifescience 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 IIb
Date Registered
Nov 26, 2024
Last Updated
Feb 3, 2024
Relationship Type
Address
Aviation Business Park Enterprise Close
Christchurch, England, United Kingdom
Postcode: BH23 6NX
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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, temporary, preformed, single-use
Type: General Medical Device
Registered: Nov 26, 2024
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Dental implant suprastructure, permanent, preformed
Type: General Medical Device
Registered: Nov 26, 2024
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Dental implant suprastructure, temporary, preformed, single-use
Type: General Medical Device
Registered: Nov 26, 2024
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