Orthosis suspension unit - UK MHRA Medical Device Registration

Orthosis suspension unit is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 166950. The device is manufactured by Coyote O&P, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Advena 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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Orthosis suspension unit

MHRA Device ID: 166950•Ref: 166950

Device Type

General Medical Device

Devices

Orthosis suspension unit

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Dec 20, 2023

Manufacturer Information

Name

Coyote O&P, Inc.

Address

419 N Curtis Rd.

Boise, ID, United States

Created Date

Feb 22, 2023

Authorized Representative

Name

Advena Ltd

Relationship Type

UK Responsible Person

Address

Pure Offices Plato Close

Warwick, England, United Kingdom

Postcode: CV34 6WE

DJ Fang

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Other Products from Coyote O&P, Inc. (1)

External lower-limb prosthesis socket, non-customized

Type: General Medical Device

Registered: Nov 26, 2024

Other Products from Same Authorized Representative (10)

Orthosis suspension unit - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

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