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General| Brand | Drive |
|---|---|
| Model | AGF-5X |
| Category | Medical Equipment |
| Language | English |
Explains pain as a warning system and the body's method of telling us something is wrong.
Defines Transcutaneous Electrical Nerve Stimulation as a drug-free method of pain control.
Describes how TENS units send electrical impulses to stimulate nerves and modify pain perception.
Covers skin irritation, pacemakers, heart conditions, carotid sinus, and transcerebral stimulation.
Includes consulting doctors for implants, avoiding machinery operation, turning off before electrode handling, and avoiding explosive atmospheres.
Addresses patients with heart disease, pregnancy, central pain origin, physician supervision, and symptomatic treatment.
Covers interference with monitoring equipment, risk of electrocution, electrode placement near throat, and abrupt control changes.
Includes keeping out of reach of children and legal restrictions on sale by physician order.
Describes the AGF-5X DIGITAL SD TENS as a battery-operated pulse generator with two channels and user-friendly controls.
Identifies key components like lead connectors, intensity control, pulse rate control, and the LCD display.
Details dual channels, pulse amplitude, asymmetrical biphasic square pulse waveform, and voltage.
Specifies power source (9V battery), size, weight, and pulse rate/width ranges.
Outlines selectable timers, burst mode, and modulation modes (M, S1, S2) with their parameters.
Lists replaceable parts such as electrode leads, electrodes, batteries, and PCB.
Details standard accessories like adhesive electrodes, leads, batteries, manual, and carrying case.
Explains graphic symbols used on the device label, including operating instructions and electrical protection.
Explains how pulse duration and pulse rate affect stimulation intensity and sensation.
Describes Normal, Burst, and Modulated modes and their effects on treatment.
Discusses typical treatment times and the duration of pain relief after cessation.
Details how to adjust pulse rate (Hz) using buttons and the recommended range of 70-120 Hz.
Explains the use of the mode button to select between Burst (B), Constant (N), and Modulation (M, S1, S2) modes.
Describes adjusting pulse width (uS) and the recommended setting of 70-120 uS.
Explains how to increase or decrease pulse width using the respective buttons.
Details the selectable treatment timer settings (15, 30, 60 minutes) and automatic shut-off.
Guides on checking and replacing the battery, ensuring intensity controls are off.
Guides on inserting lead wires into the device sockets and attaching them to electrodes.
Warns against jerking wires and plugging them into AC sockets to prevent breakage or shock.
Provides instructions for cleaning lead wires with a damp cloth and using talcum powder.
Advises consulting a clinician for electrode type and following application procedures for optimal results.
Emphasizes electrode placement importance and describes contiguous and bracket placement methods.
Offers advice on washing skin, managing excess hair, and avoiding stretching patches to prevent irritation.
Details steps for cleaning skin, connecting lead wires, and applying electrodes firmly to the treatment site.
Instructs on how to carefully remove electrodes by lifting the edge and avoiding pulling lead wires.
Provides guidance on storing electrodes in a resealed bag and improving adhesion with water.
Introduces the slide cover for controls and the Power On/Off switch, explaining intensity adjustment.
Explains how turning the intensity control clockwise increases stimulation strength.
Advises on charging rechargeable batteries before first use and after storage.
Provides instructions for charging, including using the correct outlet and following manufacturer guidelines.
Recommends non-flammable cleaning solutions and avoiding liquids or submerging the device.
Covers packing the device for transport and storage conditions (temperature, humidity).
Warns against charging non-rechargeable batteries and warns about battery incineration.
Lists weekly checks for external damage, output sockets, operating elements, and labels.
Guides on checking parameters, cable connections, battery, and cables for malfunctions.
States compliance with IEC 60601-1-2 and IEC 60601-1 safety standards.
Details the three-year warranty for the stimulator, covering parts and labor, and exclusions.
Provides manufacturer details (Drive Medical Design & Manufacturing) and contact information.
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