Knee/ankle/foot orthosis - UK MHRA Medical Device Registration

Knee/ankle/foot orthosis is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 128559. The device is manufactured by Millet Innovation from France, classified as General Medical Device. The authorized representative in the UK is Advena 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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Knee/ankle/foot orthosis

MHRA Device ID: 128559•Ref: 128559

Device Type

General Medical Device

Devices

Knee/ankle/foot orthosis

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Aug 1, 2024

Manufacturer Information

Name

Millet Innovation

Address

309 Allée des Lavandes Loriol Sur Drome

Loriol Sur Drome, France

Created Date

Dec 27, 2021

Authorized Representative

Name

Advena Ltd

Relationship Type

UK Responsible Person

Address

Pure Offices Plato Close

Warwick, England, United Kingdom

Postcode: CV34 6WE

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Other Products from Millet Innovation (10)

Other Products from Same Authorized Representative (10)

Knee/ankle/foot orthosis - UK MHRA Medical Device Registration

Device Type

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Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

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