Care Orchestrator

By Philips Belgium Commercial

Care Orchestrator gives you the power to remotely monitor and manage all of your sleep apnea and respiratory patients with a single system. It turns raw clinical data into actionable patient insights delivered directly to care teams—via smart phone, tablet or PC. So everyone can work together to make fast, informed clinical decisions, help identify which patients are at risk, and act decisively to provide timely care to those who need it.

Level 1

I am a CE-certified medical device

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General description (provided by company)

Main purpose

Care Orchestrator gives you the power to remotely monitor and manage all of your sleep and respiratory patients with a single system.

Target audience

Care Orchestrator is intended to be used by hospital, Care institutions and home care providers.

Approach

Care Orchestrator is intended to support clinical users / clinical assistants 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, 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.

Connectivity to sensors and platforms

CareOrchestrator supports sleep and respiratory therapy devices from Philips

Financing and pricing model

The costs for hosting, data transmission, updates and the development of new functionalities are part of the product.

Pathology

Sleep Treatment adherence

Functions

Health Tracking

Users

Clinicians

Additional info

Compliance to M1 criteria

CE certification

Download document Granted by Philips Respironics (Self declaration) Assessed and certified meeting the requirements of:
Medical Device Directive: MDD 93/42/EEC (old regulation) Medical Device Regulation: MDR 2017/745 (new regulation) In Vitro Diagnostic Directive: 98/79/EC (old regulation) In Vitro Diagnostic Regulation: IVDR 2017/746 (new regulation)
Certificate granted on 15/04/2019 Certificate valid till 31/12/2028 Class type of medical device (More info): 1
ISO Standards:
ISO 13485 Quality Management Systems for Medical Devices (on company level) ISO 14155 Clinical Investigations of Medical Devices in Human Subjects ISO 14971 Risk Management of Medical Devices ISO 27000 series: Information Security Management Systems ISO 62304 Medical Device Software Lifecycle Processes ISO 62366 Application of Usability Engineering to Medical Devices

FAMHP registration and notification

Company registration number at FAMHP: 60924 Product identification code at FAMHP: 582767

General Data Protection Regulation (More info)

Company declares explicitly to be compliant with GDPR rules Company declares that the data are stored in EU only

The app is only available through prescription

User instructions

Philips Respironics creates your customer account and a System Administrator user to give your organization or location access to Care Orchestrator. This System Administrator can create other administrator and clinical users / clinical assistants in Care Orchestrator, but the System Administrator does not have clinical user / clinical assistant access to Care Orchestrator.

Components of the application

Web application

Complaints handling

Via e-mail: software.support@philips.comVia telephone: 18003456443

Media

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