Enraf Nonius TENSMED S82 Instructions For Use Manual
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Enraf Nonius TENSMED S82 Instructions For Use Manual

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TENSMED S82
INSTRUCTIONS FOR USE
14. September 2020
1727751-51

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Summary of Contents for Enraf Nonius TENSMED S82

  • Page 1 TENSMED S82 INSTRUCTIONS FOR USE 14. September 2020 1727751-51...
  • Page 2 1727751-51...
  • Page 3 DEAR CUSTOMER THANK YOU FOR CHOOSING THIS PRODUCT. WE REMAIN AT YOUR ENTIRE DISPOSAL FOR ANY ASSISTANCE OR ADVICE YOU MAY NEED The device has been manufactured in compliance with applicable technical standards and has been certified, in compliance with Directive 93/42/EEC as amended by directive 2007/47 on medical devices, by the Notified Body Kiwa Cermet Italia, Via Cadriano 23, 40057 Granarolo Dell’Emilia (BO) Italy (n.

  • Page 4: Table Of Contents

    Table of contents TECHNICAL FEATURES ......................... 5 Device .............................. 5 Use conditions ..........................5 Technical features of the currents NMES and TENS: ..............5 EQUIPMENT ............................6 INTENDED USE ............................6 CONNECTIONS ........................... 7 Accessories ............................7 LABELLING AND SYMBOLS ......................... 7 WARNINGS AND CONTRAINDICATIONS..................

  • Page 5: Technical Features

    TECHNICAL FEATURES Device Size: 130 X 80 X 20 mm Weight: 220 g. Case: in ABS Protection level: IP 22 Storage and transportation temperature: from -10°C to 45°C Max. relative humidity: 30% - 75% Medical device classification class: The values indicate the limits allowed if the product or its accessories are not in the original package.

  • Page 6: Equipment

    - domestic environment; - general pain treatments; - beauty and sport purposes. The Tensmed S82 is intended to be used, and shall only be used, by or under the supervision of professional users in physiotherapy, rehabilitation and adjacent areas. 1727751-51...

  • Page 7: Connections

    It is important to read the following instructions carefully before using your Tensmed S82. The manufacturer cannot be held responsible for the results of using this device for any purposes other than described in these operating instructions. Should the use of this device lead to an undesirable event such as death or...
  • Page 8 It indicates that this device has type BF parts. WEEE symbol (Waste of Electrical and Electronic Equipment). Recycling symbol. The WEEE symbol used for this product indicates that the device may not be disposed of as a household product. Properly dispose of the product to help protect the environment.
  • Page 9 Charger Electrodes It refers to the production lot It indicates the product code It refers to product certification and indicates that complies with directive 93/42/CEE + 47/2007CEE. It indicates the storage temperature of the electrodes It refers to the expiry date ...

  • Page 10: Warnings And Contraindications

     Do not remove the electrode by grabbing the connector.  Electrodes should not touch each other.  Do not apply the electrodes on the temples, the neck and in a transthoracic way.  Do not leave the electrodes in the car. Display Working phase Battery...

  • Page 11: Warnings Before Use

    The unit should be connected to the mains by its power supply unit. Before starting the treatment, make sure that the power system specifications comply with the directives in force within your country. Make sure that the power supply unit will be in a comfortable position and that it will be easy to be removed.

  • Page 12: Side Effects And Contraindications

     The cables of the electrostimulation should not be wrapped around people's neck to avoid any risk of strangulation and suffocation;  The mobile and fixed radio communications devices could influence the functioning of the electromedical device: see the tables attached to this manual. Preventative measures to take using the device for incontinence treatments.

  • Page 13: Maintenance And Cleaning

    It is recommended to use the device with caution in people with capillary fragility, as an excessive stimulation could cause capillary ruptures. MAINTENANCE AND CLEANING Maintenance and cleaning of the device  In case of real or alleged malfunction, do not tamper with the device or try to repair it yourself. Do not intervene on the device and do not open it.
  • Page 14 We suggest charging the device for 8-12 hours to obtain the greater duration of the battery pack. A possible increase in the temperature in the battery area during the charge is normal. Do not use a different charger from the one provided with the device. To replace the electro- stimulator batteries, contact an authorized service center.

  • Page 15: Instructions For Use

    INSTRUCTIONS FOR USE 1727751-51...
  • Page 16 1727751-51...
  • Page 17 Programming By pressing the Fn button for 2 seconds in the starting screen, you will have the possibility to program the device through 6 ways ( PED1 – PED6 ). To move from a parameter to the next one press OK. PED1: It is possible to set the values of frequency and pulse width.

  • Page 18: Electrostimulation

    PED6: It is possible to set the values of tHOLD e tOFF. From 1 to 30 s in steps of 1 s. Time values for tUP and tDOWN are fixed (at 1 s) and can not be modified). It is possible to set the frequency values from 1 to 150 Hz in steps of 1 Hz. Value of the pulse width set on 300 µs (fixed).
  • Page 19 The muscle contracted in the following way: when a person decides to make a movement, an alteration of the electric potential in the motor center of the brain and an electric impulse is transmitted to the muscle that has to move. The electrical impulse is transmitted as a change of potential (voltage);...

  • Page 20: Tens

    - the current amount - the duration of the stimulus that must be adapted to the corporeal district that is wanted to be stimulated. From this consideration, for the excitation of a tissue, the relationship between the duration and the intensity of the stimulus is particularly important and not only the value of the peak of the intensity.

  • Page 21: Incontinence Programs

    The pain decrease following to the TENS currents application is due to these factors: a. Gate control theory b. Endorphin secretion c. Different sedative effects in relation with the frequency Gate theory If the electric signals that lead to the brain information about pain are stopped, also the pain perception is eliminated.

  • Page 22: Program List

    Because of the presence of clinical programs, this product is a medical device. Therefore it is certified by the Kiwa Cermet Italia Body n. 0476 according to the 93/42/EEC EU directive for medical devices. The certification covers clinical applications. CE0476 does not refer to non-medical treatments. Name Type Tensmed S82 DEMO SPORT Motor point pen SPORT Warm-up lower limbs...
  • Page 23 Name Type Tensmed S82 TENS* Lumbago P 31 TENS* Epicondylitis P 32 TENS* Scapulo-humeral periarthritis (shoulder) P 33 TENS* Carpal tunnel P 34 Osteoarthritis TENS* P 35 Menstrual pain TENS* P 36 Ankle prevention SPORT-PREVENTION P 37 Knee prevention SPORT-PREVENTION...
  • Page 24 GENERAL NOTES ON ELECTRODE POSITIONING The correct electrode positioning and the correct choice of their size are critical aspects for the electrostimulation to be effective. To choose the size of the electrodes and as for their positioning it is necessary to refer to the images at the end of this manual.

  • Page 25: Treatment Descriptions

    TREATMENT DESCRIPTIONS Following is a short description of the programs provided by the electrostimulator. SPORT WARM-UP: Increases muscular temperature for better training preparation. Increases the blood flow to and metabolism of the muscle. Recommended before training sessions or com- petitions. Intensity: low or intermediate.
  • Page 26 systems by means of a mechanical effect. The purpose is to improve blood circulation and enable the toxin elimination. Intensity: low to inter- mediate. LIPOLYSIS: The low frequency of this program positively affects the metabolism and increases the elimination of toxins and excess fluid. This is a method for reshaping critical areas, modifying the metabolism of lipocytes.

  • Page 27: Warranty

    TENS (Cervical pains, Lumbago, Periarthritis, Epicondylitis, Sciatica, …): Uses mechanisms of the nervous system to alleviate both acute and chronic pain. Impulses travel along the nerves to block the pain propagation paths. This program combines stimulation with light contractions that stimulate the release of endorphins.

  • Page 28: Frequently Asked Questions

    In order to take advantage of the warranty service, the user must comply with the following warranty clauses: 1. The products, and all accessories, to be repaired must be sent by and at the expenses of the customer in their original packages. 2.
  • Page 29 Does the power decrease using Y cables? The power intensity for each channel does not vary. However, when Y cables are used to split one single channel in two, the current is distributed on a wider muscle area, therefore contraction will be less pronounced.
  • Page 30 ELECTRODE PLACEMENT FOR NMES TREATMENTS Biceps brachii muscle Triceps brachii muscle Flexor carpi muscle Extensor carpi muscle Deltoid muscle Pectoral muscle Pectoral muscle Trapezius muscle Trapezius muscle 1727751-51...
  • Page 31 ELECTRODE PLACEMENT FOR NMES TREATMENTS Latissimus dorsi muscle Latissimus dorsi muscle Infraspinatus muscle Lumbar muscles Lumbar/Dorsal muscles Abdominals Abdominals Abdominals Rectus abdominis muscle 1727751-51...
  • Page 32 ELECTRODE PLACEMENT FOR NMES TREATMENTS Gluteus Gluteus Biceps femoris muscle Adductors Rectus femoris muscle Quadriceps Gastrocnemius muscle Gastrocnemius muscle Tibialis anterior muscle 1727751-51...
  • Page 33 ELECTRODE PLACEMENT FOR TENS TREATMENTS Shoulder pain Elbow pain Cervical pain Lumbar pain Lumbar pain Sciatica Knee pain Knee pain Knee pain 1727751-51...
  • Page 34 EMC ACCOMPANYING DOCUMENTS Essential performance PERFORMANCE CONDITION RISK ACCEPTED EVENT Electrostimulation. External Display information no The machine must stop the stimulation. disturbance longer readable. The machine must maintain the (Burst). stimulation and accept the commands. Lack of internal Interruption of the The machine must signal the battery power supply.
  • Page 35 1727751-51...
  • Page 36 Copyright: Enraf-Nonius B.V. Vareseweg 127 | 3047 AT | Rotterdam | The Netherlands Tel: +31 (0)10-20 30 600 | info@enraf-nonius.nl...

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