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Explains various symbols used on the equipment and in the manual for user understanding.
Defines symbols related to packaging, handling, and storage conditions for the product.
Provides definitions for abbreviations and lists figures referenced in the manual.
Introduces the manual's purpose and details the SONOPULSE III's features and basic operation.
Explains safety symbols and provides initial precautions for safe operation.
Outlines specific warnings and dangers related to electrical hazards, patient conditions, and flammable environments.
Lists conditions for which therapeutic ultrasound is commonly indicated and associated conditions.
Details precautions for using ultrasound, including areas to avoid and patient considerations.
Lists specific conditions and areas where therapeutic ultrasound should not be applied.
Describes potential sensations or effects experienced by the patient during or after ultrasound application.
Defines eligible patient age, weight, consciousness, and sensitivity for ultrasound therapy.
Outlines user knowledge requirements, language availability, and device mobility characteristics.
Instructions for inspecting the unit upon receipt and handling shipping damage claims.
Provides step-by-step instructions for setting up and initial care of the SONOPULSE III.
Guidelines for proper installation, operation, and maintenance to prevent security risks.
Steps for cleaning the device using water, mild soap, or antimicrobial cleaner.
Information on proper disposal of the device and its accessories due to heavy metals and waste regulations.
Details the device's power requirements, class, protection, and automatic voltage selection.
Information on the protection fuse, its replacement, and the use of fuses and power stabilizers.
Discusses potential interference, device classification, and recommendations for coexistence with other equipment.
Details conformity to standards for RF emissions, harmonic emissions, and voltage fluctuations.
Specifies immunity test levels and conformity for electrostatic discharge, transients, and outbreaks.
Guidance on power supply quality, magnetic field levels, and related immunity requirements.
Details RF immunity test levels and provides recommended separation distances for RF devices.
Table showing separation distances based on transmitter power and frequency to avoid interference.
Details device dimensions, power, ultrasound parameters, and conformity regulations.
Identifies and describes the controls, indicators, and connectors on the upper and rear views of the device.
Identifies and describes controls, indicators, and connectors on the frontal and lower views of the device.
Provides a numbered list detailing the function of each control, indicator, and connector on the equipment.
Explains the device display symbols and the function of the Start/Stop buttons.
Defines the function of the Select, Set, Up, and Down buttons for parameter adjustment.
Describes the ultrasound transducer and neutral conductor gel as essential accessories for operation.
Guides on connecting the power cable and observing the initial presentation and default screens.
Explains how to select parameters and program the treatment time using the device controls.
Details how to adjust ultrasound intensity and stop the treatment session.
Details the overtemperature protection mechanism that freezes the device when the transducer gets too hot.
Describes the protection message displayed when the transducer is not connected or is removed.
Guides on turning on, selecting parameters, adjusting intensity, and starting treatment.
Instructions for preparing the patient's skin and area for ultrasound application.
Explains how to perform simultaneous therapeutic application of ultrasound and electrostimulation.
Details the connection of the electrostimulator and the procedure for initiating and stopping combined therapy.
Illustrates the correct positioning of the ultrasound transducer and electrostimulation electrode for combined therapy.
Guides on selecting the desired language for the device interface.
Explains how to select pre-programmed treatment protocols and set therapy time.
Details how to program new custom protocols and access saved user protocols for personalized treatments.
Presents a comprehensive list of clinical protocols for various injuries and conditions with detailed parameters.
Information on recording and accessing custom user protocols.
Lists the accessories included with the SONOPULSE III, including part codes and descriptions.
Information on ordering replacement accessories and a warning against using non-specified parts.
Provides solutions for common issues like the equipment not turning on or functioning correctly.
Recommends annual inspection and preventive maintenance by authorized centers for safe operation.
Details IBRAMED's 18-month warranty terms, coverage, exclusions, and limitations.
Provides contact information for technical support and a DANGER warning regarding unauthorized modifications.
General| Equipment Type | Therapeutic Ultrasound |
|---|---|
| Frequency | 1 MHz and 3 MHz |
| ERA (Effective Radiating Area) | 7 cm² |
| Modes | Continuous and Pulsed |
| Duty Cycle | 20%, 50%, 100% |
| Treatment Time | 1 to 30 minutes |
| Display | LCD |
| Weight | 2 kg |
| Maximum Power | 21 W |
| BNR (Beam Non-Uniformity Ratio) | ≤5:1 |
| Pulsed Frequencies | 100 Hz |
| Timer | Digital |
| Power Supply | 100-240V~ (50/60 Hz) |
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