General internal orthopaedic fixation system implantation kit - UK MHRA Medical Device Registration

General internal orthopaedic fixation system implantation kit is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 164613. The device is manufactured by Biomet Trauma from United States, classified as General Medical Device. The authorized representative in the UK is Zimmer Biomet UK Limited.

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General internal orthopaedic fixation system implantation kit

MHRA Device ID: 164613•Ref: 164613

Device Type

General Medical Device

Devices

General internal orthopaedic fixation system implantation kit

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Apr 23, 2024

Manufacturer Information

Name

Biomet Trauma

Address

56 East Bell Drive

Warsaw, Indiana , United States

Created Date

Apr 26, 2021

Authorized Representative

Name

Zimmer Biomet UK Limited

Relationship Type

UK Responsible Person

Address

Stella Building Windmill Hill Business Park Whitehill Way

Swindon, England, United Kingdom

Postcode: SN5 6NX

DJ Fang

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General internal orthopaedic fixation system implantation kit - UK MHRA Medical Device Registration

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