Bone distraction forceps - UK MHRA Medical Device Registration

Bone distraction forceps is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 157988. 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.

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Bone distraction forceps

MHRA Device ID: 157988•Ref: 157988

Device Type

General Medical Device

Devices

Bone distraction forceps

Type

Class I

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

DJ Fang

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Bone distraction forceps - UK MHRA Medical Device Registration

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