TensCare Sonic Stim + Manuel utilisateur

Catégorie
Appareils de soins de la peau
Taper
Manuel utilisateur

Ce manuel convient également à

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Dear Customer,
Thank you for choosing Sonic Stim +. TensCare stands for high-quality,
thoroughly tested products for the applications in the areas of gentle
electrotherapy, muscle toning, continence management and pain relief
during labour.
Please read these instructions for use carefully and keep them for later use
and observe the information they contain.
Best regards,
Your TensCare Team
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Contents
1.0 INTRODUCTION 4
2.0 INTENDED USE 5
3.0 CONTRAINDICATIONS, WARNING & CAUTIONS 5
4.0 UNIT INFORMATION 10
5.0 INSTALLATION 11
5.1 BEFORE USE 11
5.2 CONNECTION 11
5.3 CONNECTION OF THE POWER ADAPTER 12
5.4 THERAPY MODE 12
5.5 DISCONNECTING 12
6.0 OPERATION 12
6.1. MEASURES WITH REGARDS TO TREATMENTS 12
6.2. OPERATING THE DEVICE 13
6.3. THE APPLICATOR 17
7.0 MAINTENANCE 18
7.1. CLEANING THE DEVICE 18
7.2. CLEANING THE APPLICATOR 18
7.3. CLEANING THE LEAD WIRE AND ADAPTER 18
7.4. CLEANING THE ELECTRODE PAD 19
8.0 TROUBLESHOOTING 20
9.0 SPECIFICATIONS AND TECHNICAL DATA 21
10.0 STORAGE 22
11.0 EMC 23
12.0 DISPOSAL OF WASTE ELECTRICAL AND ELECTRONIC
PRODUCTS (WEEE) 27
13.0 WARRANTY 28
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Symbols Used
Symbol for protection against electric shock: Type BF
This symbol on the unit means “Refer to instructions for use”.
Temperature Limitation: indicates the temperature limits to
which the medical device can be safely exposed.
Serial Number: indicates the manufacturer’s serial number so
that a specific medical device can be identified.
Disposal in accordance with Directive 2012/19/EU (WEEE)
Catalogue Number: indicates the manufacturer’s catalogue
number so that the device can be identified.
The name and the address of the manufacturer
Date of manufacture
Complies with the European Medical Device Directive
(93/42/EEC) and amended by directive 2007/47/EC
requirements. Notified body TUV Rheinland (CE01 97)
Importer Symbol
IPX7
Only for Ultrasonic head: Protected against the effects of
temporary immersion in water
Keep dry
Class II symbol
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1.0 Introduction
This manual has been written for the users of Sonic Stim +. It contains general
information on the operation, precautionary practices, and maintenance
information of the device. To maximize the use, efficiency, and life of the
device, please read the manual thoroughly and become familiar with the
controls, as well as the accessories before operating the device.
Pay attention to the following before using the Sonic Stim +:
1) Keep yourself informed of the contraindications (see chapter 3).
2) The device may not be used in proximity (i.e. less than 2 meters) to
shortwave equipment.
3) The device may not be used in so-called "wet rooms" (hydrotherapy
rooms).
The manufacturer cannot be held responsible for the results of using this
apparatus for any purposes other than those described in these operating
instructions.
Therapy possibilities
Sonic Stim + is a therapy apparatus that offers both ultrasound therapy and
electrotherapy. Pain affects the quality and enjoyment of life, especially for
those who suffer chronic pain. Sonic Stim + is an ultrasound and
electrotherapy device for the treatment of chronic and acute muscular pain.
The applicator has a radiant surface of 4.0cm2 and frequency of 1 MHz.
Combination therapy of ultrasound and electrotherapy is ideal to localise
trigger points and/or pain points.
The applicator
The ultrasound applicator for Sonic Stim + has one-frequency head. This
applicator can now supply 1 MHz ultrasound. The head has excellent beam
characteristics, meeting all requirements of the existing standards. The
excellent beam characteristics, ergonomic design and effective contact
control of the single-frequency applicator make optimal treatment possible.
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2.0 Intended Use
Sonic Stim + is a Portable Ultrasound and TENS (Transcutaneous Electrical
Nerve Stimulation) combination therapy device that generates deep
ultrasonic waves within body tissues and TENS for the treatment of selected
medical conditions such as symptomatic relief of chronic intractable pain,
post-traumatic pain and post-surgical pain, muscle spasms, and joint
contractures. Sonic Stim + is not recommended for the treatment of
malignancies.
3.0 Contraindications, Warning & Cautions
The precautionary instructions found in this section and throughout this
manual are indicated by specific symbols. Understand these symbols and
their definitions before operating this equipment. The definitions of these
symbols are as follows:
Caution: Text with a "CAUTION" indicator symbol will explain possible
safety infractions that could have the potential to cause minor to
moderate injury to an individual or damage to equipment.
Warning: Text with a "WARNING" indicator will explain possible safety
infractions that will potentially cause serious injury to an individual
and/or equipment damage.
Danger: Text with a "DANGER" indicator will explain possible safety
infractions that are imminently hazardous situations that could result
in death or serious injury.
Contraindications
Do not use over or near bone growth centres (epiphyseal discs) until
bone growth is complete.
Do not use over a healing fracture.
Do not use over the eyes.
Do not use over the heart.
Do not use over brain tissue.
Do not use on patients with demand type cardiac pacemakers.
Do not use on someone who is pregnant.
Do not use on testicles.
Do not use on patients post laminectomy.
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Do not use over an area of the spinal cord following a laminectomy.
Do not use on areas of the body that lack sensation.
Do not use on areas of post-traumatic sequelae.
Do not use if the patient has an endoprosthesis / metal implants.
Do not use on patients with implanted neurostimulation systems.
Do not use to treat malignancies nor in the region where tumours or
malignant tumours are present.
Do not use on patients who have thrombophlebitis and/or varices.
Do not use on patients experiencing septic inflammation.
Do not use on patients who have diabetes mellitus.
Do not use on patients who have osteoporosis.
Do not use over ischemic tissues in patients with vascular disease where
the blood supply would be unable to follow the increase in metabolic
demand.
Do not use over the carotid sinus nerves or arteries, laryngeal or
pharyngeal muscles.
Do not use on patients with hemorrhagic diatheses (excessive bleeding
disorders).
Do not use over areas that are under anaesthesia.
Do not use on acute injuries
Do not use on open wounds.
Do no use if patient is feverish (pyrexia).
Do not use on patient with tuberculosis.
Do not use on patients who have localized inflammation.
Cautions
Read, understand, and practice the precautionary and operating
instructions. Know the limitations and hazards associated with using any
ultrasound device. Observe the precautionary and operational decals
placed on the unit.
Keep informed of the contraindications.
Do not operate the device when connected to any other medical
device.
Do not operate this device in an environment where other devices used
intentionally radiate electromagnetic energy in an unshielded manner.
Ultrasound should be routinely checked before each use to ensure that
all controls function normally.
o Check intensity control - make sure it properly adjusts the intensity of
the ultrasonic power output in a stable manner.
o Check treatment time control - make sure it terminates ultrasonic
power output when the timer reaches zero.
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Do not use sharp objects such as pencil point or ballpoint pen to operate
the buttons on the control panel.
Handle the ultrasound applicator with care. Inappropriate handling of
the Ultrasound applicator may adversely affect its characteristics.
Before each use, inspect the Ultrasound Applicator for cracks to avoid
the ingress of conductive fluid.
Inspect Applicator cables and associated connectors before each use.
The ultrasound therapy control unit is not designed to prevent the ingress
of water or liquids. Ingress of water or liquids may cause malfunction of
internal components of the device and therefore create risk of injury to
the patient.
Caution should be used:
o with patients suspected or diagnosed with epilepsy.
o with patients suspected or diagnosed with heart problems.
Caution should be used in the presence of the following:
o When there is a tendency to haemorrhage following acute trauma
or fracture.
o Following recent surgical procedures when muscle contraction may
disrupt the healing process.
o Over the menstruating or pregnant uterus.
o Over areas of the skin which lack normal sensation.
Some patients may experience skin irritation or hypersensitivity due to the
electrical stimulation or electrical conductive medium. The irritation can
usually be reduced by using an alternate conductive medium or
alternate electrode placement.
Electrode placement and stimulation settings should be based on the
guidance of the prescribing practitioner.
Never apply electrodes over irritated or broken skin.
The device should be kept out of the reach of children.
The device should be used only with the leads and electrodes
recommended for use by the manufacturer.
Do not use in the bath or shower. The device should not be submerged
in water or other liquids as this will possibly damage the device and startle
the patient.
The use of heat and cold producing devices, such as electric heating
blankets, heating pads or ice packs, may impair the performance of the
electrodes or alter the patient's circulation and increase the risk of injury
to the patient.
The Sonic Stim + should not be used while driving, operating machinery,
or during any activity in which involuntary muscle contractions may put
the user at undue risk for injury.
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Warnings
Care must be taken when operating this device around other equipment.
Potential electromagnetic or other interference may occur to either this
device or to the other equipment, or both. Minimise this interference by
not using this device in conjunction with the other equipment.
This device may not be used in proximity (i.e. less than 2 meters) to short-
wave equipment.
Avoid exposure to direct sunlight, rain, excessive dust, moisture,
mechanical vibrations and shocks.
This device may not be used in so-called "wet rooms" (hydrotherapy
rooms).
Before administering any treatment, you should become acquainted
with the operating procedures for each program of treatment, as well as
the indications, contraindications, warnings, and precautions. Consult
other resources for additional information regarding the application of
electrotherapy and ultrasound.
Do not use solvents to clean this device.
Do not use this device if it is damaged in any way.
This device must only be serviced, repaired and opened by individuals at
authorised sales centres.
Dispose of this device in accordance with local regulations. Keep the
operating instructions with the device.
Pregnant and nursing women should use caution when using the device.
Avoid use over or near bone growth centres until bone growth is
complete.
Treatment time should not exceed 30 minutes a day.
Do not use a cell phone while operating the device.
Patients with sensitivity to the coupling gel should use caution when using
the device.
Stimulation should not be applied over the carotid sinus nerves,
particularly in patients with a known sensitivity to the carotid sinus reflex.
Stimulation should not be applied over the neck, thorax, or mouth. Severe
spasm of the laryngeal and pharyngeal muscles may occur, and the
contractions may be strong enough to close the airway or cause
difficulty in breathing.
Stimulation should not be applied trans-cerebrally (across the head),
over the carotid sinus (where the jaw meets the neck), over metal
implants or in conjunction with sleep apnea or heart monitors.
Stimulation should not be applied transthoracically. Since the
introduction of electrical current into the heart may cause cardiac
arrhythmias.
Stimulation should not be applied to swollen, infected or inflamed areas
or skin eruptions, e.g. phlebitis, thrombophlebitis, varicose veins, etc.
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Stimulation should not be applied over, or in proximity to, cancerous
lesions.
Always keep the ultrasound head in constant motion.
Use ample conductive gel with the ultrasound head to ensure good
coupling throughout the treatment. If needed, apply more when setting
the intensity.
Consult your doctor or physiotherapist if you are in any doubt whatsoever.
Danger
Patients with an implanted neurostimulation device must not be treated with
or be in close proximity to any shortwave diathermy, microwave diathermy,
therapeutic ultrasound diathermy, or laser diathermy anywhere on their body.
Energy from diathermy (shortwave, microwave, ultrasound, and laser) can be
transferred through the implanted neurostimulation system, can cause tissue
damage, and can result in severe injury or death. Injury, damage, or death
can occur during diathermy therapy even if the implanted neurostimulation
system is turned "off."
Biohazardous Materials
Handle, clean, and dispose of components and accessories that have come
in contact with bodily fluids according to national, local, and facility rules,
regulations, and procedures.
Adverse Reaction
Skin irritation, inflammation, and electrode burns beneath the electrodes are
potential adverse reactions. Perform the following procedures to avoid the
negative effects of ultrasound therapy.
Applicator Movement - If movement of the applicator is too slow, the
patient may feel periosteal pain characterized by a deep ache or pain.
If motion is too fast, or if the applicator does not maintain good contact
with the skin, the therapeutic effect of the sound waves will be reduced,
and the applicator may overheat.
Patient Susceptibility - Some patients are more sensitive to ultrasound
output and may experience a reaction similar to a heat rash. Be sure to
inspect the treatment area during and following treatment and stop
using if an adverse reaction occurs.
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Coupling - Coupling is described as contact between the applicator and
the treatment site and may be accomplished through the use of a
coupling agent, such as gel or lotion. Anything used as a coupling agent
must be highly conductive. Air is a very poor conductor of ultrasonic
waves.
4.0 Unit Information
1) TIME LED: indicates treatment times of 5 minutes, 10 minutes and 15
minutes
2) MODE LED: indicates intensity of the ultrasound Low (L), Medium (M) and
High (H).
3) TIME button: Adjusts treatment times to either 5 minutes, 10 minutes and
15 minutes
4) MODE button: Adjusts the ultrasound intensity: Low (L), Medium (M) and
High (H).
5) + button: Increases the intensity of stimulation
6) - button: Decreases the intensity of the stimulation
7) STIM LED: indicates the stimulation output state - when illuminate the
stimulation is on.
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8) POWER LED: indicates power state
9) ON/OFF switch: Power on by shifting up or power off by shifting down
10) Adapter connection point
11) Lead wire and electrode pad connection point
12) Ultrasound Head / Applicator
13) Main body
5.0 Installation
5.1 Before Use
Remove the device and all accessories from the box. Inspect the device for
damages or missing parts and/or accessories. Report any damage or missing
parts or accessories to your local dealer or retailer from which you purchased
this device.
Kit Contents
1 x Sonic Stim +
1 x Instruction manual
1 x Electrode (50x100mm)
1 x Lead wire
1 x Power adapter
1 x Ultrasound transmission gel (85g)
1 x Quick start guide
5.2 Connection
Prior to connecting this device to the power supply, verify that the voltage
and frequency stated on the rating label match the available power supply.
The power adapter is a part of the supply circuit on which the device's safety
depends on. The approvals for the Sonic Stim + are only valid if used in
combination with the type of adapter provided with the device.
Caution: It is not permitted to connect Sonic Stim + to any other type
of adapter other than adapter provided.
Caution: Connection of accessories other than the ones specified
by the manufacturer can adversely affect the safety of the patient
and the proper function of the equipment; therefore, it is not
permitted.
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5.3 Connection of the power adapter
1) Connect the power adapter to the device's
power cord.
2) Connect the power adapter to the wall outlet.
5.4 Therapy Mode
Sonic Stim + offers 2 treatment modes:
1) Combination: Ultrasound + Electrical Stimulation therapy
2) Ultrasound: Ultrasound therapy
5.5 Disconnecting
1) Turn off the Sonic Stim + by switching power ON/OFF switch from ON to
OFF position.
2) Remove the power adapter from the wall outlet.
6.0 Operation
6.1. Measures with regards to treatments
Before treatment
Ensure there are no contraindications to treatment.
Clean the skin of the treatment area with soap or alcohol (70%).
If the skin has excess hair, trim or shave hair for optimal treatment.
Apply a reasonable amount of ultrasound transmission/conductive gel to
the treatment area. Use only the ultrasound gel with CE mark.
Ultrasonic Action Function Test: Place the probe horizontally, then apply
several water drops on the surface of the probe, turn the device on and
press the time button to activate the ultrasound device. You will be able
to observe the ultrasonic action as the water droplets will appear to be
dancing on the sound head and you may notice a small amount of
steam being released. The water droplets on the probe start to perform
one million vibrations per second showing the atomization phenomenon.
During treatment
Move the ultrasound-head in a circular motion. The area treated should
be twice the size of the diameter of the applicator.
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If experiencing poor transmission of ultrasound energy, it is advised to add
more gel or reposition the ultrasound-head.
Caution: The ultrasound-head should be moved in a slow, flat,
circular motion over the skin surface of the treatment area. Apply
the sound head evenly (in time) over the treatment area; not too
slow to avoid inducing heat; not too fast to prevent bad contact which would
reduce the effectiveness of the treatment.
After treatment
Clean the contact surface immediately after each treatment. Make sure
that no ultrasound gel remains on the treatment head. We recommend
cleaning the head and cable daily, using lukewarm water - do not
immerse the device in water.
The treatment heads can be disinfected using a cloth moistened with 70%
alcohol.
Check if there are any signs of improvement (e.g. pain, circulation or
mobility).
6.2. Operating the device
6.2.1 Ultrasound Therapy
1) Apply Transmission Gel
Apply a layer of ultrasound transmission gel on the
treatment area. The gel acts as a coupling substance
and ensures effectiveness. The area treated should be
two times the diameter of the treatment head.
Caution: Never apply the gel to the
applicator. The applicator will register this as contact and may emit
ultrasound energy, which could damage the applicator.
2) Switch on the device
Connect the power adapter according to section 5.3.
Switch on the device, using power on/off switch by
switching from OFF to ON position. The Power LED will
light green.
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3) Adjusting intensity
Press the MODE button to select the ultrasound intensity.
The intensity has three levels, Low (L), Medium (M) and
High (H), each level corresponds to a light indicator.
4) Adjusting treatment time
Press the TIME button to cycle through the treatment
time (5, 10 and 15 minutes), as shown by the Time LED.
When the time is chosen, the system will start working.
During working time, the user can press the TIME button
to adjust the treatment time.
5) Start treatment
Move the treatment head in a flat, slow, circular motion
over the skin surface area that is covered with a layer
of ultrasound transmission gel. Apply the head evenly
(in time) over the treatment area.
Caution: The device has a load detection
system for safety. When the treatment head
does not have good contact with the skin,
the device will stop treatment automatically. During this time, the TIME LED will
flash slowly (l Hz). The device will not restore treatment until the contact is good.
Caution: The device has a temperature protection function. When
the temperature of the treatment head exceeds 42°C the
treatment will automatically stop and the TIME LED will flash quickly
(2Hz). The device will not restore treatment until the temperature is below 40°C.
6) Turn off the device
After the time duration has been completed, the device will automatically
revert to standby state. Once your therapy session has been completed, turn
off the device by sliding the ON/OFF switch downwards from ON to the OFF
position.
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6.2.2 Combination therapy
1) Connect the lead wire and
electrode pad to the unit
as shown by the illustrations
to the right.
Plug the lead wire into
the connection point
attached to the
device,
Connect the electrode pad with the lead wire.
Make sure all connections are securely in place.
Caution: The device must be turned off before connecting the lead
wires to the device.
2) Place electrode firmly on the skin after cleaning
and drying the treatment area.
Place the electrode pad on the area of the
body indicated by your physician or therapist.
Make sure the electrode pad is placed firmly
to the skin and has made good contact
between the skin and the pad.
3) Apply Transmission Gel
Apply a layer of ultrasound transmission gel on the
treatment area. The gel acts as a coupling substance
and ensures treatment effectiveness. The area treated
should be two times the diameter of the treatment
head
Caution: Never apply the gel to the applicator. The applicator will
register this as contact and may emit ultrasound energy, which
could damage the applicator.
4) Switch on the device
Connect the power adapter according to section 5.3.
Switch on the device, using power ON/OFF switch by
switching from OFF to ON position. The Power LED will
light green.
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5) Adjust ultrasound intensity
Press MODE button to select ultrasound intensity within
low, middle and high. The LED will be lighted to indicate
the selected intensity.
6) Adjust treatment time
Press the TIME button to cycle through the treatment
time (5, 10 and 15 minutes), as shown by the Time LED
indicators. When the time is chosen, the system will start
working. During working time, the user can press the
TIME button to adjust the treatment time.
7) Adjust stimulation intensity
Press the + button to increase the intensity of the
stimulation. Press the - button to decrease the intensity
of the stimulation. The STIM LED will flash every time the
+ or - button is pressed.
Note: The colour of the LED indicates the output
stimulation intensity.
Green light: Output intensity < 10 V;
Orange light: Output intensity 10 V.
Caution: The electrical stimulation cannot work without the
ultrasound output. Users can only adjust the stimulation intensity
after the ultrasound is working properly.
Caution: If the stimulation level is uncomfortable or becomes
uncomfortable, reduce the stimulation intensity to a comfortable
level and contact your medical practitioner if problems persist.
Caution: Move the ultrasound treatment head while you are
adjusting the stimulation intensity to prevent the local skin
temperature from becoming too high or burning.
Caution: Each step of increase output intensity is 1 V when the
output intensity less than 5V; 0.5V/step when the output intensity is
over 5V.
Caution: In the particular standard for Electrical Nerve and Muscle
Stimulators, IEC 60601-2-10, it is recommended not to exceed a
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current density of 2 mA r.m.s./cm2, otherwise skin irritations or burns can occur.
For current types that contain a DC component we recommend not to
exceed a current density of 0.2 mA/cm2.
8) Start treatment
Move the treatment head in a flat, slow, circular motion
over the skin surface treatment area that is covered
with a layer of ultrasound transmission gel. Apply the
head evenly (in time) over the treatment area.
Caution: The device has a load detection
system for safety. If the electrode pad or the
ultrasound treatment head do not have
good contact with the skin, the STIM LED and TIME LED will flash and stop
treatment after the output intensity of stimulation surpasses 5V. The intensity
will automatically but slowly increase to the setting level after the pad and
treatment head have made good contact with the skin.
Caution: The device has a temperature protection function. When
the temperature of the treatment head exceeds 42°C the
treatment will automatically stop and the TIME LED will flash quickly
(2Hz). The device will not restore treatment until the temperature is below 40°C.
Caution: The device works without vibration. You must move the
applicator with a slow but deliberate speed, flat against the
treatment area and in a circular motion around the treatment area.
After finishing the treatment, the device will enter the waiting state. It is not
recommended that the user restart treatment upon completion of therapy.
9) Turn off the device
After the time duration has been completed, the device will automatically
revert to standby state. Once your therapy session has been completed, turn
off the product by sliding the ON/OFF switch downwards from ON to the OFF
position.
6.3. The applicator
The applicator is a precision instrument. Great care is taken in the
development and production to obtain the best possible beam
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characteristics. Rough treatment (jarring or dropping) can adversely affect
these characteristics and must therefore be avoided.
7.0 Maintenance
7.1. Cleaning the device
Switch off the device and disconnect it from the power supply. The device
can be cleaned with a damp cloth. Use lukewarm water and a non-abrasive
liquid household cleaner (no abrasive, no alcohol content solution). If a more
sterile cleaning is needed, use a cloth moistened with an antimicrobial
cleaner.
Caution: Do not submerge the device in liquids. Should the unit
accidentally become submerged, contact the dealer or Authorized
Service centre immediately. Do not attempt to use the device that
has been submerged in any liquid substrate until inspected and tested by a
Service Technician Certified by an Authorized Service centre. Do not allow
liquids to enter the ventilation holes.
7.2. Cleaning the applicator
The applicator should be regularly inspected for damage, e.g. hairline cracks,
which could allow the penetration of liquids. Clean the contact surface
immediately after each treatment. Make sure that no ultrasound gel remains
on the applicator after using. We further recommend cleaning the head and
cable daily, using lukewarm water. The applicator can be disinfected using a
cloth moistened with 70% alcohol.
7.3. Cleaning the lead wire and adapter
Periodically wipe the lead wire and adapter clean with a cloth dampened
with a mild soap solution, and then gently wipe them dry. Rubbing alcohol on
the lead wire will damage the insulation and dramatically shorten their life.
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TensCare Sonic Stim + Manuel utilisateur

Catégorie
Appareils de soins de la peau
Taper
Manuel utilisateur
Ce manuel convient également à