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 164542. 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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Screw endosteal dental implant, two-piece

MHRA Device ID: 164542•Ref: 164542

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

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

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

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Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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Screw endosteal dental implant, two-piece