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Osteotomy guide, single-use - UK MHRA Medical Device Registration

Osteotomy guide, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 180413. The device is manufactured by Actis Medical Pty Ltd from Australia, classified as General Medical Device. The authorized representative in the UK is IdealMed 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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Osteotomy guide, single-use
MHRA Device ID: 180413โ€ขRef: 180413

Device Type

General Medical Device

Devices

Osteotomy guide, single-use

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Jul 19, 2024

Manufacturer Information

Address

1/18 Dequetteville

Kent Town, Adelaide, Australia

Created Date

Sep 17, 2023

Authorized Representative

Relationship Type

UK Responsible Person

Address

Unit A2, Beech House, Oaklands Office Park, Hooton Road, Hooton

Hooton, Cheshire, England, United Kingdom

Postcode: CH66 7NZ

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