Screw endosteal dental implant, two-piece - UK MHRA Medical Device Registration

Screw endosteal dental implant, two-piece is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 202300. 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.

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Screw endosteal dental implant, two-piece

MHRA Device ID: 202300•Ref: 202300

Device Type

General Medical Device

Devices

Screw endosteal dental implant, two-piece

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Sep 20, 2023

Manufacturer Information

Name

Zimmer Dental Inc

Address

1900 Aston Ave

Carlsbad, California, 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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Screw endosteal dental implant, two-piece - UK MHRA Medical Device Registration

Device Type

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Date Registered

Last Updated

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Address

Created Date

Name

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Address

DJ Fang

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Screw endosteal dental implant, two-piece

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