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Gait rehabilitation frame, manual - UK MHRA Medical Device Registration

Gait rehabilitation frame, manual is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 178844. The device is manufactured by Aretech, LLC from United States, classified as General Medical Device. The authorized representative in the UK is MedEnvoy 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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Gait rehabilitation frame, manual
MHRA Device ID: 178844•Ref: 178844

Device Type

General Medical Device

Devices

Gait rehabilitation frame, manual

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Jul 3, 2024

Manufacturer Information

Address

22446 Davis Drive Suite 187

Sterling, Virginia, United States

Created Date

Sep 12, 2023

Authorized Representative

Relationship Type

UK Responsible Person

Address

85 Great Portland Street First Floor

London, England, United Kingdom

Postcode: W1W 7LT

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