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Self-care monitoring web-based application software - ARTG 476405

Access comprehensive regulatory information for Self-care monitoring web-based application software in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is registered under ARTG number 476405 and sponsored by Freyr Australia Pty Ltd, manufactured by Huma Therapeutics Limited in United Kingdom. The device registration started on January 22, 2025.

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.

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Class IIb
ARTG 476405
Class IIb
Self-care monitoring web-based application software
ARTG ID: 476405
Good Name: Freyr Australia Pty Ltd - Self-care monitoring web-based application software
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Intended Purpose

The Huma Ig platform is a software as a medical device (SaMD) which utilises software and, to obtain health data collated via a mobile or a web app for patients on immunoglobulin therapies. The data collected may be shared with healthcare professionals to drive clinical management or be used for the physiological and non-physiological intermittent or spot-check monitoring of patients in professional healthcare facilities, such as clinics, hospitals or skilled nursing facilities, or in the patientโ€™s home setting. The Huma Ig app comprises modules and functionalities that are tailored to support patients on immunoglobulin therapies and help them navigate the complex, region-specific care pathways and treatment administration processes. Clinical information collected can be displayed on a clinician web portal and patient app with the addition, trend visualisation, goal setting and communication channels between clinicians and patients. The data displayed on the mobile or web app and the web portal can be labelled, flagged and triaged for the purposes of monitoring disease, itsโ€™ deterioration or improvement, to support clinical decision making and to encourage self management of disease by the patients. The platform may also provide data analytics, risk scores and static algorithms that may assist in the assessment of risk prediction, disease monitoring, prognostication and treatment dosage titration. The Huma Ig platform can be used for adult and paediatric populations with functionality to accommodate data entry by caregivers and guardians. The Huma Ig platform is not intended for use in high-acuity environments, such as ICU or operating rooms.

Device Classification
Risk Class
Class IIb
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
476405
Start Date
January 22, 2025
Effective Date
January 22, 2025
Manufacturer
Country
United Kingdom
Address
13th Floor Millbank Tower, 21-24 Millbank, London, SW1P 4QP