Craniotomy kit - UK MHRA Medical Device Registration

Craniotomy kit is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 180414. 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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Craniotomy kit

MHRA Device ID: 180414•Ref: 180414

Device Type

General Medical Device

Devices

Craniotomy kit

Type

Custom-made

Date Registered

Nov 26, 2024

Last Updated

Jul 19, 2024

Manufacturer Information

Name

Actis Medical Pty Ltd

Address

1/18 Dequetteville

Kent Town, Adelaide, Australia

Created Date

Sep 17, 2023

Authorized Representative

Name

IdealMed Limited

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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Other Products from Actis Medical Pty Ltd (4)

Other Products from Same Authorized Representative (10)

Craniotomy kit - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Address

Created Date

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