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 164721. The device is manufactured by Bodypoint, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is MDSS-UK RP 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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Ankle/foot orthosis

MHRA Device ID: 164721•Ref: 164721

Device Type

General Medical Device

Devices

Ankle/foot orthosis

Type

Class I

Date Registered

Jan 13, 2023

Last Updated

Dec 23, 2023

Manufacturer Information

Name

Bodypoint, Inc.

Address

558 1st Avenue South, Suite 300

Seattle, WA, United States

Created Date

Jan 13, 2023

Authorized Representative

Name

MDSS-UK RP LIMITED

Relationship Type

UK Responsible Person

Address

6 Wilmslow Road, Rusholme

Manchester, England, United Kingdom

Postcode: M14 5TP

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Ankle/foot orthosis - UK MHRA Medical Device Registration

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