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In this section general Warnings and Precautions are listed, that you should be aware of when using the 
TensMed 931. See also chapter 4 for Warnings and Precautions, that apply to Muscle Stimulation 
applications in particular. 
 

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Federal law (USA only) restricts this device to sale by, or on the order of, a physician or licensed 
practitioner.  

This device should be used only under the continued supervision of a physician or licensed 
practitioner. 

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Do not operate the unit in an environment of short-wave or micro-wave diathermy use as this can 
result in burns beneath the electrodes.

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Care must be taken when operating this equipment around other equipment.  Potential 
electromagnetic or other interference could occur to this or to the other equipment. Try to 
minimize this interference by not using other equipment in conjunction with it.

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Electronic monitoring equipment (such as ECG monitors and ECG alarms) may not operate 
properly when electrical stimulation is being utilized. 

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This equipment is not suitable for use in the presence of flammable anaesthetic mixture with air, 
oxygen, or nitrous oxide.

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This device should be kept out of the reach of children.

 

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Read, understand and practice the precautionary and operating instructions. Know the limitations 
and hazards associated with using any electrical stimulation device. Observe the precautionary 
and operational decals placed on the unit 

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Do not operate the TensMed 931 when connected to any unit other than Enraf-Nonius BV 
devices.

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This unit should be operated in temperatures between 10 °C and 40 °C (50 °F and 104 °F), with a 
Relative Humidity ranging from 10%-90%.

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Do not expose the unit to direct sunlight, heat radiated from a heat radiator, excessive amounts of 
dust, moisture, vibrations and mechanical shocks.

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In the case of ingress of liquids, unplug the unit from the mains supply and have it checked by an 
authorized person (see the paragraph on technical maintenance).

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Do not use sharp objects such as a pencil point or ballpoint pen to operate the buttons on the 
control panel as damage may result.

 
Before administering any treatment to a patient you should become acquainted with the operating 
procedures for each mode of treatment available, as well as the indications, contraindications, warnings 
and precautions. Consult other resources for additional information regarding the application of 
electrotherapy. 
 
 

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Relaxation of muscle spasms. 

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Prevention or retardation of disuse atrophy. 

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Increasing local blood circulation. 

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Muscle re-education. 

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Immediate post-surgical stimulation of calf muscles to prevent venous thrombosis. 

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Maintaining or increasing range of motion. 

Summary of Contents for TensMed 931

Page 1: ...7HQV0HG User Manual...

Page 2: ...Copyright Enraf Nonius B V P O Box 12080 3004 GB Rotterdam The Netherlands Tel 31 0 10 20 30 600 Fax 31 0 10 20 30 699 info enraf nonius com www enraf nonius com Part number 1427754_41 August 2005...

Page 3: ...7HQV0HG Operating Instructions...

Page 4: ...URGHV 7 1 Before treatment 8 7 2 Self adhesive electrodes 8 7 3 Electrolytic effects 8 7 4 Current density 8 7 5 Connection and disconnection reactions 8 2SHUDWLQJ QVWUXFWLRQV 8 1 Operator Controls 9...

Page 5: ......

Page 6: ...Liability law implies amongst other things that once a period of 10 years has elapsed after a product has been brought into circulation the manufacturer can no longer be held responsible for possible...

Page 7: ...ions and hazards associated with using any electrical stimulation device Observe the precautionary and operational decals placed on the unit Do not operate the TensMed 931 when connected to any unit o...

Page 8: ...conductive medium The irritation can usually be reduced by using an alternative conductive medium or alternate electrode placement See also chapter 3 Precautionary Instructions for general Warnings a...

Page 9: ...ly fitted press the ON OFF button once and the LCD display will start up and the LED Lights will come on Press the ON OFF button again to switch the unit off Use only AA Alkaline 1 5 volt batteries LR...

Page 10: ...2 10 the maximum permissible current density is 2 mA RMS per cm With the rubber electrodes this requirement is automatically met as the output current of the stimulator is limited to 50 mA RMS With s...

Page 11: ...ters that can be selected are Waveform Frequency Pulse Width Ramp Up Work Time Ramp Down Rest Time Synchronous Alternating Timer The 3 86 function interrupts a Program which is using the Timer It only...

Page 12: ...selected The first segment lights as soon as intensity is above zero Each subsequent segment represents approx 4 5V 6 V in high intensity mode 6DIHW IHDWXUHV If the unit is accidentally switched on an...

Page 13: ...tangular Rectangular unipolar alternating Treatment time 10 20 30 45 60 90 minutes or continuous Synch Alternating Synchronous between Ch1 and Ch2 Ramp Time 0 5 0 seconds in steps of 0 25 seconds Work...

Page 14: ...s is restricted to one program allowing change of Intensity and Timer only Any manual settings in 3URJUDPV 6 RU 7 will be retained if doctor lock is set You may therefore prescribe and lock any TENS s...

Page 15: ...y the performance of the unit When the electrodes initially lose their adhesive quality it is possible to reactivate the adhesiveness by applying a fine spray of water When used on clean skin and stor...

Page 16: ...put current into 1kOhm maximum setting P LJXUH Rectangular Monophasic Alternating Waveform Output current into 500 Ohm LJXUH Timing Relationship between L1 and L2 Pulses PULSE WIDTH POSITIVE AMPLITUDE...

Page 17: ...class according to IEC 60601 1 type BF Dimensions 144 x 80 x 27 5 mm h x w x d Weight 180 gr incl Batteries Environmental conditions for transport and storage Temperature 10 to 50 C Relative humidity...

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