Metal-polymer composite spinal interbody fusion cage - UK MHRA Medical Device Registration

Metal-polymer composite spinal interbody fusion cage is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 178738. The device is manufactured by LDR Medical from France, 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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Metal-polymer composite spinal interbody fusion cage

MHRA Device ID: 178738•Ref: 178738

Device Type

General Medical Device

Devices

Metal-polymer composite spinal interbody fusion cage

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Sep 6, 2023

Manufacturer Information

Name

LDR Medical

Address

Parc D'Enterprises du Grand Troyes Quartier Europe de l'Ouest 5 rue de Berlin

Sainte Savine, France

Created Date

Oct 13, 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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Metal-polymer composite spinal interbody fusion cage - 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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