Pure Global

Clinical data collection/management information application software - ARTG 470407

Access comprehensive regulatory information for Clinical data collection/management information application software in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 470407 and sponsored by Philips Electronics Australia Ltd, manufactured by Respironics Inc in United States of America. The device registration started on November 26, 2024.

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.

Free Database
Powered by Pure Global AI
TGA ARTG Official Data
Class IIa
ARTG 470407
Class IIa
Clinical data collection/management information application software
ARTG ID: 470407
Good Name: Philips Electronics Australia Ltd - Clinical data collection/management information application software
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Intended Purpose

Care Orchestrator is intended to support clinicians by tracking data on patients who are prescribed compatible therapy devices in accordance with the intended use of those therapy devices. Care Orchestrator provides remote patient data collection and viewing and is intended to be used by healthcare representatives (e.g., Physicians, Clinicians, Clinical Users / Clinical Assistants, Durable Medical Equipment providers) in conjunction with compatible non-life support therapy devices to adjust prescription and/or performance settings. Care Orchestrator allows read-only access to patients. Care Orchestrator is intended to be used in hospital, institutional, provider, and home care settings.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
470407
Start Date
November 26, 2024
Effective Date
November 26, 2024
Manufacturer
Country
United States of America
Address
1001 Murry Ridge Lane, Murrysville, PA, 15668-8550