Australia TGA ARTG record

Cushion, <specify>

Australia TGA ARTG Registered Device · ACI Group Australia · Trulife Limited · Class I · Started August 11, 2020

Good Name: ACI Group Australia - Cushion, <specify>

Device classification

Risk Class: Class I
Product Type: Single Device Product
ARTG Category: General

Registration information

Start Date: August 11, 2020
Effective Date: August 11, 2020

Sponsor

Name: ACI Group Australia

Manufacturer

Name: Trulife Limited
Country: Ireland
Address: Airton Road, Tallaght, Dublin 24

Intended purpose

A device used to provide support and comfort or assist the user to fulfil a functional requirement, e.g. sitting, lying, toiletting or nursing. In some cases it may also assist to alleviate pressure to body parts when the patient is immobilized for longer periods of time or has little body fat. A cushion is typically designed to achieve an intended purpose and will be made to suit that particular anatomical body part or supportive function.

About this record

Access comprehensive regulatory information for Cushion, <specify> in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by ACI Group Australia, manufactured by Trulife Limited in Ireland. The device registration started on August 11, 2020.

This page provides complete registration details including sponsor information, manufacturer details, and regulatory compliance data from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's complete medical device registry with 131,000+ devices, helping global MedTech companies navigate TGA regulations efficiently.