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 168959. The device is manufactured by Biomet 3i LLC 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.

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Dental implant suprastructure, temporary, preformed, single-use

MHRA Device ID: 168959•Ref: 168959

Device Type

General Medical Device

Devices

Dental implant suprastructure, temporary, preformed, single-use

Type

Class IIb

Date Registered

Sep 23, 2024

Last Updated

Sep 20, 2023

Manufacturer Information

Name

Biomet 3i LLC

Address

4555 Riverside Dr

Palm Beach Gardens, Florida, United States

Created Date

Oct 14, 2022

Authorized Representative

Name

Biomet 3i UK Ltd

Relationship Type

UK Responsible Person

Address

1 Glass Wharf Burges Salmon Rep Office

Bristol, England, United Kingdom

Postcode: BS2 0ZX

DJ Fang

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Dental implant suprastructure, temporary, preformed, single-use - UK MHRA Medical Device Registration

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Created Date

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Address

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Dental implant suprastructure, permanent, preformed

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Dental implant suprastructure, temporary, preformed, single-use

Dental implant suprastructure, temporary, preformed, single-use

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