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Summary of Contents for Richmar US 1000 3RD EDITION
- Page 1 US 1000 3RD EDITION INSTRUCTION MANUAL...
- Page 2 US 1000 3rd Edition Stimulator 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 Device Information 1.2 Medical Background 2. SAFETY INFORMATION _________________________________ 5 2.1 Contraindications 2.2 Warnings, Cautions, Adverse Reactions 3. PRESENTATION _______________________________________ 9 3.1 Construction 4. SPECIFICATIONS ______________________________________ 9 4.1 Accessories 4.2 Technical information 5. -
Page 4: General Information
1. GENERAL INFORMATION 1.1 Device Information The US 1000 3rd Edition generates deep ultrasonic waves within body tissues for the treatment of selected medical conditions such as relief of pain, muscle spas, and joint contractures, but not for the treatment of malignancies. -
Page 5: Safety Information
2. 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, Cautions, Adverse Reactions
2.2 Warnings, Cautions and Adverse Reactions WARNINGS: This device should be used only under the continued supervision of a licensed physician or practitioner. 2. The long-term effects of ultrasound are unknown. Ultrasound devices DO NOT have any curative value. 3. DO NOT use on patients with hemorrhagic diathesis. 4. - Page 7 CAUTIONS: Federal law (USA) restricts this device to sale by or on the order of a physician. 2. This device is for single patient use only. 3. Keep yourself informed of the contraindications. 4. This device is not intended for use on an unattended patient who is non-compliant, emotionally disturbed, has dementia, or low IQ.
- Page 8 12. DO NOT use on the region of blood-lacking tissue, because there is not enough blood supplied to meet the metabolic demand, so that the tissues would result in necrosis. 13. For the patient with bleeding physique, DO NOT use US 1000. WARNING The device complies completely with all parts of 21 CFR 1050.
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Page 9: Presentation
3. PRESENTATION 3.1 Construction LED INTENSITY INDICATOR TREATMENT HEAD ON/OFF & HI/MED/LO BUTTON MAIN BODY GRIP ASSISTANCE MAIN BODY SPEC. LABEL DC RECEPTACLE 4. SPECIFICATIONS 4.1 Accessories DESCRIPTION Ultrasound Device (DU1025) Wall Adapter (DU1025X) Therasonic Ultrasound Gel (LC2828) Instruction Manual Carrying Case (CC1006) -
Page 10: Technical Information
4.2 Technical Information Waveform Pulse Power supply Switch adapter( Input: AC100-240V, 50/60Hz, Output:DC24V/0.2A) Operating 10°C to 40°C, 40% to 90% Relative Conditions Humidity Storage/Transportation -10°C to 60°C, 30% to -95% Conditions Relative Humidity Dimensions 6.80 x 2.25 x 1.65 inches (L*W*H) Weight 4.25 ounces Frequency... -
Page 11: Instructions For Use
5. INSTRUCTIONS FOR USE Steps to Connect the Adapter 1. Insert the DC Plug of the adapter into the DC receptacle on the main unit. (as the picture). 2. Please hold the main unit tightly, when inserting the DC plug into the DC. Insert and pull out the DC plug in correct direction. -
Page 12: Function Test Of Ultrasonic Action
Begin Treatment Use gentle upward or circular motions with the treatment head on treated area. Keep the treatment head gliding over the skin, CAUTION DO NOT stop moving the treatment head as it could cause potential burns or injury. Turning Off the Device The device will automatically shut down after working 30 minutes with 5 beeps. -
Page 13: Maintenance And Cleaning
6. 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 14: Troubleshooting
8. 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 15: Electromagnetic Compatibility (Emc) Tables
9. 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 16 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 17 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 18 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 19 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 20: Glossary Of Symbols
10. 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 21: Warranty
11. 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 six months from date of purchase. - Page 22 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 24 Manufactured for: 3289.19.06.A ©2019 Compass Health Brands Corp.
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