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INDEX Chapter Contents Page Index…………….....................………………………………….1 1. Introduction.………………………………………………………2 2. Cautions .……………………………………………………….…2 3. Warnings.……………………………………………………….…3 4. General Description.……………………………………….….…4 5. Construction...…………………………………………………...5 6. Technical Specifications..……………………………………….6 7. Replaceable Parts...…………………………………………..….7 8. Accessories....…………………………………………………….7 9. Graphic Symbols...……………………………………………....8 10. Parameter Controls............……………………………….…....9 11.
TENS devices can affect the operation of demand type cardiac pacemakers. TENS is not recommended for patients with known heart disease without physi- Chapter 1 : INTRODUCTION EXPLANATION OF DIGITAL EMS cal evaluation of risk. Do not use TENS on the carotid sinus(neck) region. Do no apply TENS for undiagnosed pain syndromes until etiology is established. Do Electrical Muscle Stimulation is an internationally accepted and proven way of treating muscular injuries.
may not operate properly when EMS stimulation is in use. 8. There should be a prominently placed statement warning that stimulus deliv- Chapter 5 : CONSTRUCTION ered by this device may be sufficient to cause electrocution. Electrical current of this magnitude must not flow through the throax because it may cause a cardiac arrhythmia. 9. Do not place electrodes on the front of the throat as spasm of the Laryngeal and Pharyngeal muscle may occur. 10.
Chapter 6 : TECHNICAL SPECIFICATION Chapter 7 : REPLACABLE PARTS The technical specification details of AGF-6X DIGITAL DIGITAL EMS are as follows. The replaceable parts and accessories of DIGITAL EMS devices are as given below – MECHANISM 01. Channel TECHNICAL DESCRIPTION Dual, isolated between channels. 02. Intensity Control Adjustable 0-90mA, Max output 90mA peak to peak (17.8mA rms) into 500ohm load each 01 PARTS ELECTRODES LEADS channel.
II.LABEL Chapter 10 : PARAMETER CONTROLS The label attached to the back of devicecontains important message about this device- model, serial number, sup- PULSE DURATION ply voltage, the name of manufacturer, CE number and classification. Please do not remove. Wider pulse duration settings will deliver stronger stimulation for any given intensity setting.
Perception – The intensity is increased so that the patient can feel the stimulation, but there is not any muscular contraction. Chapter 11 : ATTACHMENT OF ELECTRODE LEAD WIRES Slight Contraction – Intensity is increased to a barely visible muscular contraction that is not strong enough to move a joint. When using low pulse rate The wires provided with the system insert into the jack sockets settings, this will show as individual twitches.
Chapter 14 : ELECTRODE PLACEMENT MULTIPLE PLACEMENT STRATEGIES The placement of electrodes can be one of the most important parameters in achieving success with DIGITAL EMS therapy. Of utmost importance is the will- Because the DIGITAL EMS has two independently operated channels, the clinician may take advantage of concurrent pad placement strategies. ingness of the clinician to try the various styles of electrode placement to find which method best fits the needs of the individual patient.
Chapter 16 : APPLICATION OF RE-USABLE SELF ADHESIVE ELECTRODES Application 1. Clean and dry the skin at the prescribed area thoroughly with soap and water prior to application of electrodes. 2. Insert the lead wire into the pin connector n the pre-wired electrodes. Important 1. Do not apply to broken skin. 2. The electrodes should be discarded when they are no longer adhering. 3. The electrodes are intended for single patient use only. 4. If irritation occurs, discontinue use and consult your clinician. 5.
4. Lead Connector Connection of the electrodes is made with two-lead connector. The device must be switched off before connecting the cables. Both intensity controls must be at the Off position. Electrodes must be pressed firmly on the skin. 8. Function Indicator The drawing on the top of LCD showing the function that is working. Each part of the drawing represents one function of the course. Ramp Up 5. Function Selector Expose the controls by sliding front cover down from top of unit.
b. Set Contraction Time The contraction time controls the time of stimulation. By pressing parameter f. Set Pulse Width The pulse width determines the length of time. Each electrical signal is ap- controls, the contraction time can be pre-set. The range is adjustable from 1 second to 30 seconds. plied through the skin, which controls the strength and sensation of the stimulation. The pulse width is adjustable from 2 to 250 uS. Press the buttons until the desired value is reached. c.
RECHARGEABLEBATTERIES: Prior to the use of a new unit, the rechargeable battery should be charged according to the battery manufacturer’s instructions. Before using the battery charger, read all instructions and cautionary markings on the battery and in this instruction manual. After being stored for 60 days or more, the batteries may lose their charge. After long periods of storage, batteries should be charged prior to use.
Chapter 21 MALFUNCTIONS All AGF-6X Digital EMS models carry a warranty of one year from the date of delivery. The warranty applies to the stimulator only and covers both parts and labour relating thereto. Should any malfunctions occur while using the DIGITAL EMS, check - whether the controls or parameters are set to the appropriate form of therapy. Adjust the control correctly.
