Richmar US 1000 3RD EDITION Скачать руководство пользователя страница 16 | Manualshive

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Richmar US 1000 3RD EDITION Скачать руководство пользователя страница 16

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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
CISPR 11

Group 1

The device uses RF energy only for
its internal function. Therefore, its RF
emissions are very low and are not likely
to cause any interference in nearby
electronic equipment.

RF emissions
CISPR 11

Group B

The device is suitable for use in all
establishments including domestic and
those directly connected to the public
low-voltage power supply network that
supplies buildings used for domestic
purposes.

Harmonic emissions
IEC 61000-3-2

Class A

Voltage
fluctuations/flicker
emissions IEC
61000-3-3

Applicable

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Содержание US 1000 3RD EDITION

Страница 1: ...INSTRUCTION MANUAL US 1000 3RD EDITION...

Страница 2: ...r notice Amendments may however be published in new editions of this manual All Right Reserved Rev V2 2019 United States Federal Law restricts this device to sale by or on the order of a physician or...

Страница 3: ...NS _______________________________________ 9 4 1 Accessories 4 2 Technical information 5 INSTRUCTIONS FOR USE ________________________________ 11 5 1 Function Test of Ultrasonic Action 6 MAINTENANCE A...

Страница 4: ...US 1000 is a Therapeutic ultrasound device that generates pulsed high frequency sound waves 1MHz that are transferred to a specific body are via a sound headed probe The Pulsed Sound Waves travel dee...

Страница 5: ...DO NOT use for patients with demand type cardiac pacemakers 7 DO NOT use on someone who is pregnant 8 DO NOT use over ischemic tissues in patients with vascular disease where the blood supply would b...

Страница 6: ...device away from children 6 DO NOT use over an area of the spinal cord following laminectomy i e when major covering tissues have been removed 7 Avoid bony prominences 8 When using ultrasound keep th...

Страница 7: ...tor or any other metallic or electronic device should not use this device without first consulting a doctor 9 Patients with the following diseases or symptoms should not use the device Pregnancy or Me...

Страница 8: ...r the patient with bleeding physique DO NOT use US 1000 WARNING The device complies completely with all parts of 21 CFR 1050 10 of the performance standard for sonic infrasonic and ultrasonic radiatio...

Страница 9: ...LED INTENSITY ON OFF MAIN BODY INDICATOR HI MED LO BUTTON TREATMENT HEAD MAIN BODY 4 SPECIFICATIONS 4 1 Accessories NO DESCRIPTION QTY 1 Ultrasound Device DU1025 1 2 Wall Adapter DU1025X 1 3 Therason...

Страница 10: ...Humidity Dimensions 6 80 x 2 25 x 1 65 inches L W H Weight 4 25 ounces Frequency 1MHz 10 Type Non focusing Pulse Width 8 0 5ms 10 14 1ms 10 29 2ms 10 Repetition Rate 150 Hz 10 Temporal Maximum Power 4...

Страница 11: ...s and will void warranty Apply Transmission Gel Wash the area to be treated so that it is free of oil and dirt Apply a generous layer of ultrasound transmission gel on the treatment area The gel acts...

Страница 12: ...er shut down press the On Off button and hold down for 4 seconds and the device will turn off 5 1 Function Test of Ultrasonic Action Place the probe horizontally then apply several water drops on the...

Страница 13: ...ected and tested by a Service Technician certified by an Authorized Service Center Cleaning the Applicator The applicator should be regularly inspected for damage e g hairline cracks which could allow...

Страница 14: ...cal distributor or the manufacturer as shown on the label PROBLEM CHECK POINTS POSSIBLE SOLUTION LED light does not turn on 1 The plug adapter is not inserted into the socket properly 2 The DC plug of...

Страница 15: ...interferences as well as maximum levels of electromagnetic emissions for medical devices Medical devices manufactured by Compass Health Brands Corp conform to this IEC50501 1 2 2007 standard for both...

Страница 16: ...up 1 The device uses RF energy only for its internal function Therefore its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment RF emissions CISPR 11...

Страница 17: ...000 4 4 2 kV for power supply 2 kV for power supply Main power quality should be that of a commercial or hospital environment If the user of the device requires continued operation during power mains...

Страница 18: ...frequency range b Interference may occur in the vicinity of equipment marked with the following symbol Radiated RF lEC 61000 4 3 3 V m 80 MHz to 2 5 GHz 3 V m NOTE I At 80 MHz and 800 MHz the separati...

Страница 19: ...e according to frequency of transmitter m 150 kHz to 80 MHz 80 MHz to 800 MHz 800 MHz to 2 5 GHz 0 01 0 12 0 12 0 23 0 1 0 37 0 37 0 74 1 1 17 1 17 2 33 10 3 69 3 69 7 38 100 11 67 11 67 23 33 For tra...

Страница 20: ...sposed 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 Please contact the organization...

Страница 21: ...manufacturer to the consumer or during transport to the retailer Accessories which are subject to normal wear and tear Liability for direct or indirect consequential losses caused by the unit is exclu...

Страница 22: ...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 7 Returns will not be accepted on items that are...

Страница 23: ...23...

Страница 24: ...Manufactured for 3289 19 06 A 2019 Compass Health Brands Corp...

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