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Table of Contents
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Summary of Contents for PHILIPS Respironics Actiwatch Spectrum PRO
- Page 1 Actiwatch Technician Guide...
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Page 2: Intended Use
In addition, the Actiwatch Spectrum PRO device has a built-in score pad that allows the subject to subjectively assign and enter a numeric score. The score pad can be used as a substitute or in addition to the traditional patient diary used in conjunction with activity data recording. -
Page 3: System Contents
System Contents Your package may include some or all of the following for your appropriate system. Spectrum PRO or Plus USB Cable Wearer Guide (10 pack) Actiware Software Technician & Clinician Guides Replacement Watchbands and Tool Actiwatch Spectrum Communication Dock Wearer Guide (10 pack) Actiware Software Technician &... - Page 4 Preparing Actiwatch for a Patient 1. Launch the Actiware software application. (See the Software Installation Guide for system requirements and complete installation instructions.) 2. Open the database where the data will be stored by selecting File > Database > Open. Then, select the desired database.
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Page 5: Recharging The Battery
Connect your communication dock to your computer, and then position the device on the communication dock as shown on the previous page. Note: For Actiwatch 2, Philips Respironics recommends fully charging before storage or use. Fully charging may require 24 hours depending upon prior use. -
Page 6: Maintenance
Maintenance It is recommended that Actiwatch be returned to Philips Respironics after one year of field use for preventative maintenance. The expected service life of Actiwatch is five years. WEEE Recycling Directives Separate collection for electrical and electronic equipment per EC Directive 2002/96/EC. -
Page 7: Specifications
15% to 95% RH non-condensing non-condensing non-condensing Actiwatch Spectrum PRO/Plus Power Input: 4.25 to 5.25 VDC, 100 mA Standards Compliance This device is designed to conform to the following standards: IEC 60601-1: 2005 - Medical Electrical Equipment Part 1: General Requirements for Safety IEC 60601-1-2: 2007 - Medical Electrical Equipment Part 1-2: General Requirements for Safety. -
Page 8: Emc Information
EMC Information Guidance and Manufacturer’s Declaration – Electromagnetic Emissions This Device is intended for use in the electromagnetic environment specified below. The user of the Device should assure that it is used in such an environment. Emissions Test Compliance Electromagnetic Environment - Guidance This Device uses RF energy only for its internal function. - Page 9 Guidance and Manufacturer’s Declaration – Electromagnetic Immunity This Device is intended for use in the electromagnetic environment specified below. The user of the Device should assure that it is used in such an environment. Immunity Test IEC 60601 Test Level Compliance Level Electromagnetic Environment - Guidance Portable and mobile RF communications equipment should be used no...
- Page 10 Recommended Separation Distance Between Portable and Mobile RF Communication Equipment and the Device. The Device is intended for use in the electromagnetic environment in which radiated RF disturbances are controlled. The user of the Device can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communication equipment (transmitters) and the Device as recommended below, according to the maximum output power of the communications equipment.
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Page 11: Warranty
Warranty Respironics warrants that the Actiwatch Spectrum PRO device, the Actiwatch Spectrum Plus device, the Actiwatch 2 device and communication dock, and the Actiwatch Spectrum device and communication dock (each a “Product”) will be free from defects in materials or workmanship for a period of one (1) year from the date of delivery to the purchaser. - Page 12 1104768 1104715 R01 JDH 04/24/2013...
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