Funnel chest remodelling bar - UK MHRA Medical Device Registration

Funnel chest remodelling bar is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 138855. The device is manufactured by Biomet Microfixation from United States, classified as General Medical Device. The authorized representative in the UK is Zimmer Biomet UK Limited.

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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Funnel chest remodelling bar

MHRA Device ID: 138855•Ref: 138855

Device Type

General Medical Device

Devices

Funnel chest remodelling bar

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Apr 23, 2024

Manufacturer Information

Name

Biomet Microfixation

Address

1520 Tradeport Drive

Jacksonville , Florida , United States

Created Date

May 18, 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

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Funnel chest remodelling bar - UK MHRA Medical Device Registration

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