United Kingdom MHRA device registration 164721

Ankle/foot orthosis

United Kingdom·General Medical Device·Bodypoint, Inc.·Registered Jan 13, 2023

Registration details

Device ID: 164721
MHRA Reference Number: 164721
Date Registered: Jan 13, 2023
Last Updated: Dec 23, 2023

Device classification

Device Type: General Medical Device
Devices: Ankle/foot orthosis
Type: Class I

Manufacturer

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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About this record

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.

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