Hip/knee/ankle/foot orthosis - UK MHRA Medical Device Registration

Hip/knee/ankle/foot orthosis is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 129570. The device is manufactured by OPPO Medical Inc. from United States, classified as General Medical Device. The authorized representative in the UK is MT Promedt Consulting 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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Hip/knee/ankle/foot orthosis

MHRA Device ID: 129570•Ref: 129570

Device Type

General Medical Device

Devices

Hip/knee/ankle/foot orthosis

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 25, 2024

Manufacturer Information

Name

OPPO Medical Inc.

Address

Seattle City Centre, 1420 Fifth Ave., Ste. 220080

Seattle, Washington, United States

Created Date

Dec 30, 2021

Authorized Representative

Name

MT Promedt Consulting Ltd

Relationship Type

UK Responsible Person

Address

Beaver House, 23-38 Hythe Bridge Street

Oxford, England, United Kingdom

Postcode: OX1 2EP

DJ Fang

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Other Products from OPPO Medical Inc. (8)

Other Products from Same Authorized Representative (10)

Hip/knee/ankle/foot orthosis - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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