Ankle/foot orthosis - UK MHRA Medical Device Registration

Ankle/foot orthosis is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 80737. The device is manufactured by POD Active Pty Ltd from Australia, classified as General Medical Device. The authorized representative in the UK is Wellkang 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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Ankle/foot orthosis

MHRA Device ID: 80737•Ref: 80737

Device Type

General Medical Device

Devices

Ankle/foot orthosis

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Apr 16, 2024

Manufacturer Information

Name

POD Active Pty Ltd

Address

Level 3, 115 Myers Street

Geelong, Victoria, Australia

Created Date

May 14, 2021

Authorized Representative

Name

Wellkang Ltd

Relationship Type

Authorised Representative (Northern Ireland)

Address

Enterprise Hub, NW Business Complex 1 Beraghmore Road

Derry, Northern Ireland, Northern Ireland, United Kingdom

Postcode: BT48 8SE

DJ Fang

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Other Products from POD Active Pty Ltd (1)

Knee support orthosis

Type: General Medical Device

Registered: Nov 26, 2024

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Ankle/foot orthosis - UK MHRA Medical Device Registration

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