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SHOULDER PACEMAKER

TM

 - User Manual 04-06EN 

13 

 

INSTRUCTIONS FOR USE 

We strongly recommend that you carefully read the contraindications and safety measures described  in  the "Intended Use" chapter of this 
manual. 

 

Preliminary checks 

 

Make sure the stimulator battery is fully charged before each use session. 

 

Make sure that at least 2 electrodes are available to stimulate the muscles of interest. 

 

Check that the environmental and safety requirements described above are met. 

Positioning of the electrodes 

It is important to use the electrodes provided in the kit and to position 
them correctly on the muscle group you wish to stimulate in order to 
ensure  the  effectiveness  of  the  treatment.  Always  follow  the 
positioning  instructions  shown  in  the  following  figures,  except  in  the 
case of specific medical indications. 
Remark:  an  approximate  positioning  of  the  electrodes  makes  the 
session  less  effective,  but  it  does  not  constitute  a  danger,  except  for 
the contraindications described in this manual. 
The  electrode  is  positioned  in  the  area  of  the  nerve  supplying  the 
hypoactive  muscles.  Simultaneous  stimulation  of  agonist  and 
antagonist  should  be  avoided  because  of  the  resulting  movement 
restriction.  One  electrode  is  placed  inferior  to  the  spina  scapulae  to 
stimulate the external rotators (M. infraspinatus, M. teres minor). The 
second electrode is placed medially to the margo medialis scapulae to 
stimulate  the  scapula  retractors  (M.  trapezius  pars  transversa,  Mm. 
rhomboidei). 
 

Positioning of the stimulator 

Place a layer of skin protection in the area of the arm that will be in contact with the stimulation device. Ensure that the protective layer covers 
the  skin  and  avoids  direct  contact  between  it  and  the  stimulation  device.  The  stimulator  is  posteriorly  equipped  with  an  elastic  band  to  be 
positioned around the right or left arm based on the side of the pathology to be rehabilitated. Make sure Velcro fixing is stable on the arm. The 
device must be properly positioned in order to guarantee the correct connection of the cables to the electrodes. To check correct positioning, 
connect the conductor cables  to the electrodes taking care to keep the device switched off. Try to raise the arm frontally and laterally and 
check that cables are not stressed and movements are comfortable for the subject. 

                       

 

         

 

Setting of stimulation energies 

In  a  stimulated  muscle,  the  number  of  fibers  involved  depends  on  the  stimulation  energy.  For  programs  that  induce  powerful  muscular 
contractions (tetanic contractions) it is absolutely necessary to use the maximum stimulation energies, within the subject’s tolerance limits, in 
order to involve the greatest possible number of fibers. For other types of programs, which only induce muscle  contraction, the stimulation 
energies must be progressively increased to obtain clearly visible muscle twitches. 
It is important to use the maximum current intensity that the patient can comfortably tolerate, which generally increases during the course of 
the treatment, In general, it is not advisable to exceed the levels too quickly: the different levels correspond to a progressive advancement in 
training through electrostimulation. 

WARNING

: Use this device only with cables, electrodes and accessories recommended by NCS Lab. 

Summary of Contents for SHOULDER PACEMAKER SPM Series

Page 1: ......

Page 2: ...SHOULDER PACEMAKERTM User Manual 04 06EN 2 ...

Page 3: ... SUPPLIED 8 TECHNICAL FEATURES 10 INSTRUCTIONS FOR USE 13 FUNCTIONING OF THE DEVICE 15 DEVICE DESCRIPTION 15 BASIC INSTRUCTIONS 15 BEGINNING OF A STIMULATION SESSION 15 CHOICE OF THE PROGRAM 15 PROGRAM SELECTION 15 START OF STIMULATION 15 STOP AND SWITCH OFF THE STIMULATOR 15 BATTERY CHARGE STATUS AND STIMULATOR CHARGING PROCEDURE 15 ALARMS 16 PROGRAMS 16 MANUAL MODE 16 AUTOMATIC MODE 16 TRAINING ...

Page 4: ...ore using the device Shoulder Pacemaker TM This manual is an informative document and not an independent training text for the use of the product For proper training please contact our support and assistance team at the following address info shoulderpacemaker com Technical assistance is provided by our team Any problem encountered must be reported to the address provided above Our team will provi...

Page 5: ...ove function 6 7 8 It should be emphasized that not all shoulder disorders can be treated by muscle electrostimulation the competent doctor is responsible for selecting the correct indication and treatment based on the extent of the injury and the patient s medical history Conventional electrical muscle stimulation imposes a pre defined rhythm on the users patients as they need to adapt the speed ...

Page 6: ...nesia The user must receive adequate training before using the device for the first time A maximum of 30 minutes of device use is required to complete a stimulation session based on Shoulder Pacemaker TM technology PERSON DESIGNATED AS THE SUBJECT OF THE TREATMENT The person designated to be rehabilitated with the Shoulder Pacemaker TM device is a person who can express himself understand and exec...

Page 7: ...imulator Do not use the Shoulder Pacemaker TM device in areas where unprotected equipment is present for the emission of electromagnetic radiation Portable communication devices can interfere with electro medical devices In case of doubt about the use of the stimulator near another medical device contact the manufacturer of the device in question or the doctor The recommended operating temperature...

Page 8: ...with the limits for a Class B digital device pursuant to part 15 of the FCC Rules These limits are designed to provide reasonable protection against harmful interference in a residential installation This equipment generates uses and can radiate radio frequency energy and if not installed and used in accordance with the instructions may cause harmful interference to radio communications However th...

Page 9: ...nd MySPM Home applications must be installed on a mobile phone tablet compatible with BLE communication and that runs on the Android operating system version 6 0 onwards and with at least 100MB of free disk space to allow installation and saving files The SPM01K3 kit configuration contains 1 electrostimulator REF SPM01 MySPM application REF SPM01A1 Medical device according to Directive 93 24 EEC a...

Page 10: ...d from each other Shape of the pulses compensated biphasic wave in order to exclude any component of direct current and avoid residual polarizations on the skin Maximum pulse intensity instantaneous value 300 mA Maximum intensity of the pulses intended as an effective value mediated on 1s 10 mA Duration of a pulse 10 to 200 μs Maximum amount of electricity for one pulse 10 2 microcoulombs Pulse fr...

Page 11: ...IEC 61000 3 2 Not applicable Voltage fluctuations flicker emissions IEC 61000 3 3 Not applicable Table 1 electromagnetic emissions Guidance and manufacturer s declaration electromagnetic immunity Shoulder Pacemaker TM is designed to operate in the electromagnetic environment specified below The customer or user of the device should ensure that it is used in such an environment Proof of Immunity Te...

Page 12: ...the transmitter frequency Proof of Immunity Test level of IEC 60601 Level of compliance Recommended separation distance d RF Irradiate IEC 61000 4 3 10 V m da 80 MHz a 2 7 GHz 10 V m d 30 cm Proximity field immunity from IEC 61000 4 3 RF wireless communication devices TETRA 400 380 390 MHz 27 V m 27 V m d 30 cm GMRS 460 FRS 460 430 470 MHz 28 V m 28 V m LTE Band 13 17 704 787 MHz 9 V m 9 V m GSM 8...

Page 13: ... protection in the area of the arm that will be in contact with the stimulation device Ensure that the protective layer covers the skin and avoids direct contact between it and the stimulation device The stimulator is posteriorly equipped with an elastic band to be positioned around the right or left arm based on the side of the pathology to be rehabilitated Make sure Velcro fixing is stable on th...

Page 14: ...5 seconds P1 Training 7 seconds P2 Training 9 seconds P3 Training 11 seconds P4 Only for the SPM01K2 SPM01K3 SPM01K4 kits Wireless mode W The Manual Operating program M is performed at the beginning of the usage session to let the patient familiarize with the muscle sensation induced by stimulation The program allows the user to adjust the intensity of stimulation with a wheel followed by a phase ...

Page 15: ...rt immediately after selecting the program The selection of the program must be confirmed by pressing the button As long as the choice is not confirmed the red led in correspondence of the selected program is in flashing mode If the program has been erroneously selected do not confirm the selection with the button and turn the wheel to return to the program selection phase START OF STIMULATION The...

Page 16: ...ditions static phases and then activate it again when these conditions are no longer verified To establish the level of stimulation initially the subject manually chooses the maximum tolerated stimulation value Manual selection implies that the subject by rotating the wheel progressively increases the intensity of the stimulation Once the maximum tolerated intensity level has been reached the subj...

Page 17: ...t the stimulator is switched off Proceed by disconnecting the conductive cables from the stimulator and insert the USB charging cable in the space provided Then connect the cable to a power supply capable of delivering 5V and at least 275mA Wait until the device has been recharged signaled by the complete lighting of the red LED band REPLACEABLE PARTS The replaceable parts of the system which requ...

Page 18: ...ge the position of the electrodes slightly Stimulation causes discomfort The electrodes lose their adhesiveness and no longer provide adequate contact with the skin then they must be replaced The electrodes are worn and must be replaced Change the position of the electrodes slightly The device does not work Check that the device is charged If the device still does not work contact our customer ser...

Page 19: ...REF V 25 50 75 100 125 150 maximum value FSTIM Hz 35 typical value TSTIM μs 100 typical value ZLOAD Ω 500 extreme precautionary value 2000 typical value 5000 Table 5 Stimulation parameters and load resistances considered in the example tables ZLOAD 500 Ω TSTIM 100 μs FSTIM 35 Hz VREF 25 50 75 100 125 150 VPEAK V 24 43 48 85 73 28 97 71 122 13 146 56 VEFF_STIM V 10 06 20 11 30 17 40 23 50 29 60 34 ...

Page 20: ...re and system updates and for software problems troubleshooting during product use contact the NCS Lab support team info ncs company com info shoulderpacemaker com 39 059 669813 Via Pola Esterna 4 12 41012 Carpi MO The e mails sent to the above address will be replied within 48 hours ...

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