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General| Brand | Human Tecar |
|---|---|
| Model | HCR 1002 |
| Category | Medical Equipment |
| Language | English |
Describes the technology behind HCR 1002 using high-frequency alternating current.
Explains the trademarks TECAR® and TECARTERAPIA® and their usage.
Details the physiological effects of energy transfer and its therapeutic application.
Specifies the professional qualifications needed to use the HCR 1002 device.
Symbol indicating the need to consult the user guide before using the device.
Symbol indicating that instructions are supplied electronically.
Symbol indicating potential device malfunction or damage due to incorrect instructions.
Symbol indicating Type BF applied part for electrical safety.
Symbol for equipotential bonding bar, important for electrical safety.
Symbol representing alternating current.
Symbol for a fuse.
Symbol indicating CE marking compliance with European directives.
Symbol indicating separate disposal as per WEEE directive.
Symbol indicating potential non-ionizing radiation emissions.
Symbol for manufacturer identification.
Symbol for the year of manufacture.
Symbol for the manufacturer's code number.
Symbol for the manufacturer's serial number.
Symbol indicating important warnings, precautions, or operating instructions.
Lists the components of the HCR 1002 device, including the control unit and accessories.
Details the components of the control unit's front panel, including display and buttons.
Describes the components of the control unit's rear panel, including connections and ventilation.
Explains the function of the treatment display on the control unit.
Explains the ON/OFF switch and its corresponding LED indicator.
Describes the SETUP function, including menu selection and navigation buttons.
Details the TREATMENT section, including mode selection, start/stop, and power regulation.
Explains how electrodes are connected and distinguished by color and key input.
Details the specific color coding for the RES electrode handpiece.
Details the specific color coding for the CAP electrode handpiece.
Describes the characteristics and lifespan of high-impedance CAP electrodes.
Describes the characteristics and lifespan of low-impedance RES electrodes.
Describes the flat indifferent electrode and its features.
Describes the cylindrical indifferent electrode and its use.
Explains how to switch the device on/off and adjust output power using the remote control.
Details the electrolytic emulsion, its actions, and design.
Explains the operating principle of the HCR 1002 device and its modes (RES/CAP).
Outlines the intended use and applications of the HCR 1002 for rehabilitation and therapeutic purposes.
Provides instructions for unpacking and initial setup of the device.
Advises on initial cleaning and disinfection procedures for the device.
Details the recommended environmental conditions for transport and service of the device.
Option to adjust the device's screen brightness.
Option to adjust the device's audio volume.
Setting for enabling/disabling the end-of-session acoustic signal.
Displays the current battery charge level of the remote control.
Shows the connection status between the device and the remote control.
Provides information about the device itself.
Option to enable or disable voice processing features.
Navigates back to the main screen from the setup menu.
Detailed steps for powering the device on and off.
Guides on selecting between RES and CAP operating modes.
Instructions for starting and stopping the treatment session.
Guidance on applying electrodes and adjusting output power.
Specifies that the device must be used by qualified healthcare personnel.
Emphasizes the importance of checking accessories for damage before use.
Details patient preparation, including consent, removing metallic objects, and shaving.
Provides guidance on positioning electrodes and applying conductive emulsion.
Explains the importance of correct pressure for electrode contact and current penetration.
Guides on the appropriate speed of electrode movement during treatment.
Details how to regulate output power based on patient sensation of heat.
Provides guidelines on setting treatment duration and session frequency.
Explains the meaning of different LED signals and display alerts.
Provides warnings and precautions for using the device's handpieces.
Outlines precautions for cleaning, sanitizing, and using electrodes.
Classifies the device according to harmonized technical norms for safety evaluation.
Lists the technical specifications, including power supply, fuses, input power, and size/weight.
Classifies the device regarding hygiene and safety, recommending cleaning or disinfection.
Lists recommended and contraindicated products for cleaning and disinfection.
Provides general warnings and precautions for device safety and operation.
Specifies training requirements for technicians performing maintenance.
Lists the necessary equipment for technicians performing maintenance.
Outlines routine maintenance tasks for the device and its components.
Describes how the device and its accessories are packaged for shipping.
Provides recommendations for the safe transport of the device.
Indicates the location and content of the device's label.
Lists conditions under which the warranty may be excluded or cease.
Details circumstances that will void the device's warranty.
Explains the procedure for requesting technical support.
Outlines the specifics of technical support, including costs and responsibilities.
Lists the European directives and technical standards applied to the device.
States that the device complies with EMC regulations and describes potential interference.
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