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Ankle/foot orthosis - UK MHRA Medical Device Registration

Ankle/foot orthosis is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 170805. The device is manufactured by TurboMed Orthotics Inc from Canada, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (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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General Medical Device
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Ankle/foot orthosis
MHRA Device ID: 170805•Ref: 170805

Device Type

General Medical Device

Devices

Ankle/foot orthosis

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Apr 17, 2024

Manufacturer Information

Address

240 de Sydney (101)

St-Augustin-de-Desmaures, QUE, Canada

Created Date

Apr 19, 2023

Authorized Representative

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 – UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

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Ankle/foot orthosis

Type: General Medical Device

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