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Knee distraction orthosis - UK MHRA Medical Device Registration

Knee distraction orthosis is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 120211. The device is manufactured by BAAT Medical Products B.V. from Netherlands, classified as General Medical Device. The authorized representative in the UK is Qserve Group UK, 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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Knee distraction orthosis
MHRA Device ID: 120211•Ref: 120211

Device Type

General Medical Device

Devices

Knee distraction orthosis

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Address

F. Hazemeijerstraat 800

Hengelo, Overijssel, Netherlands

Created Date

Dec 13, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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