Elbow/wrist/hand orthosis - UK MHRA Medical Device Registration

Elbow/wrist/hand orthosis is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 85942. The device is manufactured by Myomo Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Compliance Solutions (Lifesciences) 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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Elbow/wrist/hand orthosis

MHRA Device ID: 85942•Ref: 85942

Device Type

General Medical Device

Devices

Elbow/wrist/hand orthosis

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Mar 27, 2024

Manufacturer Information

Name

Myomo Inc.

Address

137 Portland Street 4th Floor

Boston, MA, United States

Created Date

Jun 19, 2021

Authorized Representative

Name

Compliance Solutions (Lifesciences) Ltd

Relationship Type

UK Responsible Person

Address

Suite 10, Dunswood House 1 Dunswood Road Cumbernauld

Glasgow, United Kingdom

Postcode: G67 3EN

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Elbow/wrist/hand orthosis - UK MHRA Medical Device Registration

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