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 169962. The device is manufactured by Dentalpoint AG from Switzerland, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (UK) Limited .
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
Nov 13, 2024
Name
Dentalpoint AGAddress
Bodenรคckerstrasse 5
Spreitenbach, Aargau, Switzerland
Created Date
Nov 11, 2021
Relationship Type
Address
Compass House, Vision Park Histon c/o Cr360 โ UL International
Cambridge, England, United Kingdom
Postcode: CB24 9BZ
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Dental implant suprastructure, permanent, preformed
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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, temporary, preformed, single-use
Type: General Medical Device
Registered: Nov 26, 2024
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