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Summary of Contents for Richmar US PRO 2000 2ND EDITION
- Page 1 US PRO 2000 2ND EDITION INSTRUCTION MANUAL...
- Page 2 US Pro™ 2000 2nd Edition Portable Ultrasound This user manual is published by Richmar. Richmar does not guarantee its contents and reserves the right to improve and amend it at any time without prior notice. Amendments may however be published in new editions of this manual.
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Page 3: Table Of Contents
TABLE OF CONTENTS 1. GENERAL INFORMATION _______________________________4 1.1 General description 1.2 Medical background 1.3 Foreword 2. IMPORTANT SAFETY INFORMATION ______________________5 2.1 Contraindications 2.2 Warnings and Cautions 3. PRESENTATION _______________________________________8 3.1 Construction 3.2 Features and Benefits 3.3 Steps to Connect the Adapter 4. -
Page 4: General Information
1. GENERAL INFORMATION 1.1 Device Information THE US PRO 2000™ 2ND EDITION is a portable ultrasound device that generates deep ultrasonic waves within body tissues for the treatment of selected medical conditions such as pain relief, muscle spasms, and joint contractures, but not recommended for the treatment of malignancies. -
Page 5: Important Safety Information
2. IMPORTANT SAFETY INFORMATION Read instruction manual before operating. Be sure to comply with all “Contraindications”, Warnings”, “Cautions” and “Adverse reactions” in the manual. Failure to follow instructions may cause harm to user or device. Safety Symbols Used in this Manual Indicates a potentially hazardous situation which, if not avoided, could result in serious injury and equipment WARNING... -
Page 6: Warnings And Cautions
2.2 Warnings and Cautions WARNINGS: DO NOT use on patients with hemorrhagic diatheses (excessive bleeding disorders). 2. DO NOT use over an area of the spinal cord following a laminectomy, i.e., when major covering tissues have been removed. 3. DO NOT use over areas that are under anesthesia. 4. - Page 7 CAUTIONS: Always use this device under the directions of a physician. 2. Patients with the following diseases, symptoms or conditions should not use the device: • During pregnancy or menstrual cycle. • Acute disease, heart disease, tubercle disease, facial neuralgia (sharp facial pain), pernicious tumor, hemophilia, high fever, abnormal blood pressure, or under any unhealthy conditions.
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Page 8: Presentation
3. PRESENTATION 3.1 Construction Time Indicator Light Time Button Power Indicator Light Intensity Indicator Light Mode Button Power Switch Ultrasound Head 3.2 Features and Benefits All the ultrasound parts are assembled and tested under strict process controls. To ensure quality, the device has been designed with a single chip microprocessor. -
Page 9: Steps To Connect The Adapter
3.3 Steps to Connect the Adapter US PRO™ 2000 2ND EDITION requires the following steps for proper setup: Ultrasound transmission gel is required when treating a patient with the US PRO™ 2000 EDITION portable ultrasound device. The AC/DC adapter is required to power the device. No battery is used. -
Page 10: Specification
4. SPECIFICATIONS Item Description Ultrasound Ultrasound Modulation 1.0MHz±10% Probe Frequency Max. Output Power 6.4W±20% (Modulation duty cycle at 100%) Output Power L: 0.32W±20% M:3.20±20% H: 6.40W±20% Pulse Repetition Rate 100Hz±10% Modulation Duty Cycle L(5%), M(50%), H (100%) Effective Radiating Area 4.0cm2±20% Waveform Pulsed... - Page 11 Buttons Time: Choose working time: 5m-10m-15m-0m (stop) Mode: Choose modulation duty cycle: 5%-50%- 100% Indication Time Indication Lights: 5, 10, 15 minutes Lights Duty Cycle Indication Low (L), Medium (M), High (H) Lights Operation 5°C - 40°C; 30% - 75%RH; 800-1060hPa Conditions...
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Page 12: Instructions For Use
5. INSTRUCTIONS FOR USE 5.1 Turning on the Device and Head Warming Feature Turn the device on by sliding the power switch upwards (towards “ON”). The power indicator light will illuminate. The device will automatically enter the preheat mode. The six indicator lights will flash alternately during this period. - Page 13 Set ultrasound intensity: Press the “MODE” button to select the modulation duty cycle. The mode button has three levels, Low (L) - 5%, Medium (M) - 50%, and High (H) - 100%, each level corresponds to a LED light indicator. Set treatment time: Press the “TIME”...
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Page 14: Load Detection System Caution
5.3 Load Detection System Caution The device has a load detection system for safety. When the treatment head does not have good contact with the skin, the device will stop treatment automatically, and the time indicator light will flash once. The device will not continue the treatment program until good contact is made. -
Page 15: Maintenance And Cleaning
7. MAINTENANCE AND CLEANING Switch off the device and disconnect it from the power supply. The device can be cleaned with a damp cloth. Use lukewarm water and a non-abrasive liquid household cleaner (no abrasive, no alcohol content solution). If a more sterile cleaning is needed, use a cloth moistened with an antimicrobial cleaner. -
Page 16: Troubleshooting
9. TROUBLESHOOTING The device is manufactured through complete quality assurance system. If there are any performance problems, please check the chart below for problems you can fix. Performance problems often result from little things that you can find and fix at home without tools. This can save you the cost of a service call. -
Page 17: Electromagnetic Compatibility (Emc) Tables
10. ELECTROMAGNETIC COMPATIBILITY (EMC) TABLES IMPORTANT INFORMATION REGARDING ELECTROMAGNETIC COMPATIBILITY (EMC) With the increased number of electronic devices such as PC’s and mobile (cellular) telephones, medical devices in use may be susceptible to electromagnetic interference from other devices. Electromagnetic interference may result in incorrect operation of the medical device and create a potentially unsafe situation. - Page 18 Guidance and manufacturer’s declaration - electromagnetic emissions The device is intended for use in the electromagnetic environment specified below. The customer or the user assures that it is used in such an environment. Emissions Test Compliance Electromagnetic environment - guidance RF emissions Group 1 The device uses RF energy only for...
- Page 19 Guidance and manufacturer’s declaration - electromagnetic immunity The device is intended for use in the electromagnetic environment specified below. The customer or the user should assure that it is used in such an environment. Immunity test IEC 60601 test Compliance Electromagnetic level level...
- Page 20 Guidance and manufacturer’s declaration - electromagnetic emissions. The device is intended for use in the electromagnetic enviroment specified below. The customer or the user of the device should assure that it is used in such an environment. Immunity IEC 60501 Compliance Electromagnetic environment guidance test...
- Page 21 Recommended separation distances between portable and mobile RF communications equipment and the device. The device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the device can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) as recommended below, according to the maximum output power of the communications equipment...
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Page 22: Glossary Of Symbols
11. GLOSSARY OF SYMBOLS Serial number Attention: Read the operating instruction before use! Equipment capable of delivering output values in excess of 10mA r.m.s. or 10V r.m.s. averaged over any period of 5s. Electrical devices are recyclable material and should not be disposed of with household waste after their useful life! Help us to protect the environment and save resources and take this device to the ap- propriate collection points. -
Page 23: Warranty
12. WARRANTY Please contact your dealer in case of a claim under the warranty. If you have to send the unit back to your provider, enclose a copy of your receipt and state what the defect is. The following warranty terms apply: The warranty period for device is one year from date of purchase. - Page 24 4. Returned merchandise must be in the same unit of measure as originally purchased. 5. Return Labels or Call Tags can be issued by our customer service department to return merchandise. 6. Associated fees and return freight charges will apply. All returns of dropshipped items are subject to a restocking fee as well as inbound and outbound freight charges.
- Page 28 Manufactured for: 3292.19.06.A ©2019 Compass Health Brands Corp.
Need help?
Do you have a question about the US PRO 2000 2ND EDITION and is the answer not in the manual?
Questions and answers
The head does not heat up. How can I tell if the machine is actually working. The lights do work.
If the head of the Richmar US PRO 2000 2ND EDITION does not heat up, follow these steps to determine if it is functioning properly:
1. Check the Power Connection – Ensure the adapter is correctly connected to both the ultrasound unit and a wall outlet. Use only the manufacturer-supplied adapter.
2. Verify the Preheat Function – The device enters preheat mode automatically when turned on. The six indicator lights should flash alternately during this process, which takes about three minutes.
3. Look for Indicator Signals – When the preset temperature is reached or the maximum preheat time ends, all indicator lights should flash five times before entering standby mode.
4. Confirm Ultrasound Operation – Even if the head does not heat, the ultrasound function may still work. Apply ultrasound transmission gel and test if the unit turns on and operates as expected.
5. Cancel the Warming Feature – Ensure the warming function is not accidentally disabled by pressing the "MODE" and "TIME" buttons simultaneously.
6. Troubleshoot with the Manual – Consult the troubleshooting section of the instruction manual for further steps.
If the device still does not heat up or function correctly, contact the manufacturer for support.
This answer is automatically generated