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Summary of Contents for ThermoTek Artek PRO
- Page 1 Cold, Heat, and Compression Therapy Unit INSTRUCTIONS FOR USE Need Help? See our instructional videos on how to set up and use your ARTEK Pro 0P1DATP01M-EN Rev X3...
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Page 2: Indications For Use
Failure to connect strangulation risk. system may cause system to leak. • Do not cast over the ARTEK Pro therapy • Only use the ARTEK Pro system with the wraps. power cord and accessories provided •... -
Page 3: Operating Principle
If your prescribed therapy is ‘as tolerated,’ you should choose therapy ON time that works best for you. Thermal therapy on the ARTEK Pro rests for 15 min and is not adjustable by the user. It is important for your safety that you do not skip the rest period. -
Page 4: Unpacking The System
(on back of the device) Vents Hose Unpacking the System The ARTEK Pro system is provided with the following components. If the packaging is damaged, or any listed pieces are missing, please contact customer service at 866.280.5844. ARTEK Pro Device Universal Therapy Wrap Kit •... - Page 5 ARTEK Pro Keyboard The ARTEK Pro device is controlled using a simple, touchpad operation. The touchpad provides the following information and control. Refer to this section during set-up and therapy instruction. Power Indicator: The power indicator will illuminate green when the system is supplied with wall power.
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Page 6: Cleaning And Maintenance
Doing so may cause the fluid to overflow out 2. To set up the ARTEK Pro, you need to of the reservoir into the overflow fill the wrap with water. Have 2 cups basin. - Page 7 Using the ARTEK Pro The ARTEK Pro system can deliver cold or heat thermal therapy that can be combined with compression therapy. Refer to your physician’s prescription on which therapy you should use and their instructions on the duration and frequency of use.
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Page 8: Troubleshooting
Troubleshooting Need Help? See our instructional videos on how to set up and use your ARTEK Pro. Device Set up Wrap and Use Application Therapy skin area is discolored, tingly, numb, blistered or is otherwise physically altered. • Terminate therapy immediately and remove the wrap. -
Page 9: Disposal Information
See the next section to identify the reason for the fault and troubleshooting tips. • Use troubleshooting tips from this section to help resolve the fault. For further information about your ARTEK Pro, visit us at www.directekusa.com/artek-pro or call us at 866.280.5844 Disposal Information Do not dispose of the device or its accessories in household waste. -
Page 10: Fault Identification
Other yellow lights may also appear on your keypad, indicating the nature of the issue. The tables below outline the faults that may present on the ARTEK Pro and the troubleshooting tips recommended to fix the issue. The Key below defines the different therapy LEDs that can illuminate yellow when a fault is present. - Page 11 Fault Identification Thermal Therapy Faults Fault Cause Troubleshooting Cold The system detects Disconnect from wall temp water temperature power for 10 min. limit lower than Reconnect and restart. expected. Disconnect and reconnect the wrap to the hose and confirm a good connection.
- Page 12 Fault Identification Compression Therapy Faults Fault Cause Troubleshooting High The system detects Reapply wrap assuring pressure wrap pressure that there are no kinks or limit higher than folds and retry. expected. Avoid any external pressure on the wrap (squeezing or pressing on the wrap) while in use.
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Page 13: Technical Information
Technical Information The ARTEK Pro system (device and accessories) comes with a 90-day manufacturer’s warranty. ARTEK Pro Technical Specifications ARTEK Pro Safety Signed Marked on the Equipment ARTEK Pro Part 0V9PTATP01UNVWRC01 Number Operating 41F - 80F [5C - 27C] Environment... - Page 14 Technical Information ARTEK Pro Guidance and Manufacture Declaration – Electromagnetic Immunity Immunity IEC 60601 Test IEC 60601 Test Electromagnetic Environment Level Level - Guidance Test Electrostatic +/- 8 kV contact +/- 8 kV contact Floors should be wood, Discharge concrete, or ceramic tile. If...
- Page 15 Technical Information 1.7 EMC Notice 1.9 MRI Notice This equipment generates, uses, and This equipment contains electronic and can radiate radio frequency energy. If ferrous components, whose operation not installed and used in accordance can be affected by intense with the instructions in this manual, electromagnetic fields.
- Page 16 The information and content within this User Manual is prprietary and confidential to ThermoTek. It may not be reproduced or distributed, in whole or in part, without the prior written permission of ThermoTek. QR Code Ref: Device Set Up and Use: 0P1PATP01QSU...
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