Page 1
Model sam-12
Ultrasonic
Diathermy
Device
Directions
for Use
Page 2
Contents
1. Introduction .............................................................................................................................................. 4
2. Indications for Use ................................................................................................................................ 4
3. Safety .......................................................................................................................................................... 5
3.1. Contraindications ................................................................................................................................... 5
3.2. Warnings .................................................................................................................................................... 5
3.3. Precautions ............................................................................................................................................... 6
4. Features of the
5.
sam Components ................................................................................................................................. 9
6. Operator Interface ............................................................................................................................... 10
7. Accessories ............................................................................................................................................ 10
8. LED Display .............................................................................................................................................. 11
9. Initial Setup Instructions ................................................................................................................... 13
10. Treatment Options ............................................................................................................................... 13
11. Application Instructions .................................................................................................................... 16
12. Device Power Down and Removal ............................................................................................... 22
13. Modes of Operation ........................................................................................................................... 23
14. Cleaning and Maintenance ............................................................................................................. 24
15. Storage and Operating Conditions ............................................................................................. 24
16. Disposal of Waste Products ........................................................................................................... 25
17. Appendix ................................................................................................................................................. 26
A. Symbols ........................................................................................................................................ 26
B. Specifi cations ............................................................................................................................. 27
C.Notice of Compliance, Calibration and Operational Period .................................... 28
sam Device .............................................................................................................. 8
D. Technical Information ............................................................................................................. 29
E. Electrical Immunity and Emissions ................................................................................... 30
F. Warranty ........................................................................................................................................ 33
G. Troubleshooting ....................................................................................................................... 34
3ZetrOZ, Inc.
Page 3
1. Introduction
Thank you for choosing the sam Ultrasonic Diathermy Device! This manual contains
general instructions for operation, application, precautions, and maintenance. In order
to obtain maximum life and effi ciency from the
operation of the device, please read and understand this manual thoroughly. This
device is only to be used as directed in this manual.
sam was developed as a next generation wearable ultrasound therapy system which
combines miniaturization technology into a small and portable ultrasound therapy
system. It is designed to work with the human body and maximize the safe and eff ective
delivery of long-duration therapeutic ultrasound. Simple to administer and operate on a
broad range of body types, sam allows the delivery of ultrasound treatment for up to
four hours. It operates at a preset frequency and allows the use of up to two applicators
simultaneously. Applicators are applied and secured to the surface of the body using
convenient
The specifi cations put forth in this manual were in eff ect at the time of publication.
sam Ultrasound Coupling Bandages.
1.1. GENERAL SAFETY
Thoroughly read and understand the precautionary and operating instructions before
attempting to operate the sam Ultrasonic Diathermy Device. Know the limitations and
hazards associated with using any ultrasound device. Observe the precautionary and
operational decals placed on the device. Periodically review the operation procedures
and safety precautions outlined in this manual.
sam Device and to assist in the proper
1.2. PRESCRIPTION USE ONLY
Caution: Federal law restricts this device to sale by or on the order of a practitioner
licensed by the law of the state in which he/she practices to use or order the
use of the device.
This device complies with 21 C.F.R. § 1050.10
2. Indications for Use
The sam Ultrasonic Diathermy Device is intended to apply ultrasonic energy to
generate deep heat within body tissues for the treatment of selected medical
conditions such as the relief of pain, the relief of muscle spasms, the treatment of joint
contractures and the local increase of circulation.
The
sam Ultrasonic Diathermy Device is a prescription use device. sam should only
be administered and monitored by a licensed healthcare practitioner.
4 Product Support 203-349-2798
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3. Safety
3.1. CONTRAINDICATIONS
Contraindications for the use of ultrasound include:
• Over an area of the body where a malignancy is known to be present
• Over the eyes
• Over or near growth centers until bone growth is complete
• Over the reproductive organs
• Over the pregnant uterus
• Over a healing bone fracture
• On the thoracic area if the patient is using a cardiac pacemaker
• Over an active implanted medical device such as an implanted deep brain
stimulation device
• On the brain, spinal cord, or large subcutaneous peripheral nerves
• Ischemic tissues in individuals with vascular disease where the blood supply
would be unable to follow the increase in metabolic demand and tissue necrosis
might result
3.2. WARNINGS
• If the treatment is reported as painful or too hot at any point during treatment,
turn off device and remove the device from the skin.
• Instruct the patient to inform the practitioner if the patient feels any pain or
burning during treatment.
• Instruct the patient how to turn off the
Applicator if the patient feels any pain or burning during treatment.
• If the Lock Switch is in the locked position it must be placed in the unlocked
position to disable the power. Locking the treatment settings is optional and not
required for treatment.
• ALWAYS administer treatment using a new
Use one sam Ultrasound Coupling Bandage per applicator. Use of the sam
Ultrasound Applicator without a new sam Ultrasound Coupling Bandage MAY
RESULT IN BURN and/or REPEATED SHUTOFF of the
• The sam Device should be kept out of the reach of children.
sam Device and remove the sam
sam Ultrasound Coupling Bandage.
sam Applicator.
5ZetrOZ, Inc. Product Support 203-349-2798
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• DO NOT apply the
replacement for the sam Ultrasound Coupling Bandage. Use of alternative
coupling media in lieu of the sam Ultrasound Coupling Bandages may reduce
the eff ectiveness of treatment, lead to automatic shutoff of the applicator, or
cause a burn.
sam Applicator with alternative coupling media as a
• DO NOT administer treatment if the applicator is not connected to a
Ultrasound Coupling Bandage.
• Applicators and
apply this device over an open wound or infl amed skin.
• DO NOT use the sam Ultrasound Coupling Bandage if the sam Ultrasound
Media is dried out. Indications of a dried out bandage include: the cup is not
full of gel, there is dry residue or fi lm in the cup, or there is any cut, break, or
opening in the bandage or seals.
• DO NOT apply directly over a bone that is near the skin surface.
sam Ultrasound Coupling Bandages are not sterile. DO NOT
sam
3.3. PRECAUTIONS
Precaution should be taken when using the device:
• Over an area of the spinal cord following a laminectomy, i.e. when major covering
tissues have been removed
• On patients with hemorrhagic diatheses
• Over areas where metal prosthesis or other metallic implants are embedded
in tissue which may form a refl ective surface to the ultrasound energy causing
unintended irradiation of tissue and excessive heating
• Over an acute infection or sepsis
• On patients with peripheral artery disease
• Over a deep vein thrombosis
• Over an anesthetized area or in conjunction with a condition that causes
impairment of sensation, such as caused by chemotherapy
• When using the
seals have been completely removed before attaching the applicator to the skin
sam Ultrasound Coupling Bandage, ensure the top and bottom
3.4. INFLAMMABLE GASES AND ANESTHETICS
• Warning: Explosion hazard if used in the presence of fl ammable anesthetics,
open fl ame, or oxygen-rich environment
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3.5. ELECTRONICS AND BATTERY
WARNINGS
• This device is rated IPX0; therefore, it is Not Waterproof. DO NOT apply a direct
stream of any liquid onto the device, submerge the device, or allow any liquid to
pool on the surface of the device. DO NOT use if device has been submerged
in water.
• This device contains a rechargeable lithium-ion battery. DO NOT disassemble,
DO NOT heat above 100°C, DO NOT incinerate or expose to water and
DO NOT ingest.
• The use of accessories, transducers and/or cables other than those specifi ed,
with the exception of those sold by the manufacturer as replacement parts for
internal components, may result in increased emissions or decreased electrical
immunity of the equipment or system.
• DO NOT open or modify any component of the
as shock, burn or inappropriate functionality can result from unauthorized
modifi cation of the sam Device.
• Use of the
aff ect the output performance and safety of the device. Do not use the device if
any abnormal functionality occurs.
PRECAUTIONS
• Only recharge the
other recharging device may result in damage to the system and void
all warranties.
• When not in use, power ‘OFF’ the device to protect the functionality of
the components.
• Avoid dropping the applicator or power controller and avoid scratching the
lens of the applicator. Rough handling may reduce the device’s acoustic output
power, thereby reducing the eff ectiveness of therapy.
• The power controller and applicators should be routinely checked for cracks and
other damage before each use to determine that the device functions normally.
• DO NOT place the device in a location where the power charging cord could be
a trip hazard.
• DO NOT use sharp objects such as a pencil point or ball point pen to operate the
buttons on the control panel as damage may result.
sam Device around electromagnetic interference may negatively
sam Device using the sam Electrical Charger. Use with any
sam Device. Hazards such
• Prevent potential electromagnetic or other interference. DO NOT open the
Device or connect the device or components of the device to any non-sam
part. Keep the device clean and make sure no exposed non-insulated wires are
visible. If damage is present, do not administer treatment.
7ZetrOZ, Inc. Product Support 203-349-2798
sam
Page 7
4. Features of the sam Device
4.1. PRESET TREATMENT
The sam Device is preconfi gured to provide continuous ultrasonic output at a preset
frequency and intensity which cannot be modifi ed by the user. The user can set the
treatment duration to be 1, 2, 3, or 4 hours.
4.2. sam ULTRASOUND APPLICATORS
The sam Ultrasound Applicators serve as the ultrasound transducers of the
sam Device. The applicators off er low-profi le design with light emitting diode (LED) on/
off notifi cation. The ergonomic plastic housing and smooth contours provide
enhanced comfort.
4.3. sam SENSING
sam is designed to work with the human body and maximize the safe and eff ective
delivery of long-duration therapeutic ultrasound. Each sam Applicator is equipped
with closed-loop continuous temperature monitoring which maintains treatment site
temperatures below 44°C during normal operation. See section 13.4 on page 24 for
more information.
4.4. sam ULTRASOUND COUPLING BANDAGES
The sam Device utilizes ultrasound coupling bandages which are manufactured with
ultrasound coupling media sealed inside. The ultrasound coupling bandages ARE
REQUIRED to secure the sam Applicators to the body.
4.5. BATTERY OPERATION
Powered by a rechargeable lithium-ion battery, the sam Device can provide
4 hours of therapy on a single battery charge.
4.6. LOCK SWITCH
The sam Power Controller Module includes a slide lock switch that allows the locking
of treatment settings so that they cannot be inadvertently modifi ed during a 1 – 4 hour
treatment session. Locking the
treatment time toggle button and the power ONOFF button. To disable the device or
modify treatment time once in locked mode, the lock switch must be moved to the
unlocked position. Similarly, the device cannot be turned on while in locked mode and
must be unlocked fi rst. The use of the locking feature is OPTIONAL.
sam Power Controller Module will disable both the
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5. sam Components
100
80
60
40
20
AT12
AT-12
PMC12
%
DONE
UB12
HRS
4
3.5
3
2.5
2
1.5
1
YB12
YB-12
CT12
if included
AT12
AT-12
fi gure 1: sam Model-12 Components
sam MODEL 12 COMPONENTS
AT-12 : Ultrasound Applicators
UB-12: Ultrasound Coupling Bandages
OM-12: User Manual
PMC-12: Power Controller Module
CT-12: Electrical Charger
YB-12: Y-branch Adapter
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6. Operator Interface
Battery
Indicator LED
Power Button
%
100
80
60
40
20
Front
Treatment
Timer LED
HRS
DONE
Charge Port
4
3.5
3.5
3
3
2.5
2.5
2
1.5
1
Indicator LED
fi gure 2: sam Interface Components
Side
Bottom
Toggle
Button
Lock Switch
Applicator
Connection
Indicator LED
7. Accessories
The sam Device may be used with any of the following accessories:
sam Belt Clip
sam Armband
sam Carrying Case
* Additional sam Ultrasound Coupling Bandages may be obtained by contacting
the manufacturer
10 Product Support 203-349-2798
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8. LED Display
The sam Device contains Light Emitting Diode (LED) displays that indicate the
functions of the device (see Figure 2).
8.1. POWER CONTROLLER INDICATOR LED
The Indicator LED provides power, charging and error checking information.
Color of Indicator LED Meaning
Opaque (absence of light) Power Controller is OFF.
No power is being generated
Blue Power Controller is ON. Note – Ultrasonic
energy is generated only when the Power
Controller is connected to the sam
Applicator(s)
Green Power Controller battery is fully charged
Amber Power Controller battery is charging
Red Too many applicators are attached. A
maximum of two applicators may be
attached to a single power controller at
any time
Table 1. Power Controller LED Color Defi nitions
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8.2. CONTROL PANEL
The front face of the sam Power Controller Module contains a control panel. The
LEDs on the control panel are divided into a fi eld for Battery Indicator and a fi eld for
Treatment Timer. The operator is able to make selections by pressing the Power Button
and the Toggle Button.
Color of Battery Indicator LED* Meaning
Red Only Low Battery, Re-Charge required
Blinking Red Re-Charge required
Amber Power Controller is partially charged
Green Power Controller fully charged
*These lights remain on for 4 seconds and subsequently turn off
Table 2. Battery Indicator LED Color Defi nitions
Treatment Time Indicator LED Meaning
Blue Treatment time remaining. Treatment
timer is set in one hour increments and
will count down in 30 minute increments
Amber Treatment complete. This single “done”
light will activate only when a treatment
cycle has completed and will remain
illuminated for 8 hours, then turn off
Table 3. Treatment Time Indicator LED Color Defi nitions
8.3. APPLICATOR INDICATOR LED
LED Color Meaning
Opaque (absence of light) Applicator is not receiving power
Blue Applicator is receiving power from the
Power Controller. Ultrasonic energy is
being generated at all times this light
is illuminated
Red (accompanied by vibration) sam Sensing Mode. No Ultrasonic energy
is being generated from this applicator
while this light is illuminated
Table 4. Applicator LED Color Defi nitions
12 Product Support 203-349-2798
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Bottom of sam Power Controller
Micro USB
Wall Charger
Outlet
9. Initial Setup Instructions
Remove the sam Device components (Figure
1) from the packaging and inspect for any damage
that may have occurred during shipment. Charge
the device for up to 6 hours or until the Power
Controller Indicator LED is Green. The
arrives only partially charged due to generally
accepted shipping practices.
9.1. CHARGING THE POWER
CONTROLLER MODULE
A. Plug the micro USB end of the sam
Electrical Charger into the charging port on
the bottom of the sam Power Controller.
B. Plug the electrical charger into a 120/230
VAC wall outlet. The
Module indicator LED will be amber. When
the device is fully charged the top right
indicator LED will change from amber
to green.
sam Power Controller
sam Device
fi gure 3A
10. Treatment Options
10.1. TREATMENT DURATION
The sam Ultrasonic Diathermy Device provides
ultrasound therapy at a preset frequency and
intensity. The user can program the treatment
duration to be 1, 2, 3, or 4 hours. The maximum
treatment duration setting on the
is 4 hours. Treatment duration should be set to
the minimum increment required for eff ective
therapy. Due to individual diff erences in skin type
and tolerance, it is recommended to begin with a
1 hour treatment. Increase treatment duration in
subsequent applications only as tolerated. Maximum
usage time is 4 hours per day per treatment area.
The
sam Device may be used while charging.
Charging the device during treatment has no impact
on device frequency or intensity output settings. If
using
sam while charging, position the device in
such a way that the charger cable is easily removed
from the power controller module if needed.
sam Device
13ZetrOZ, Inc. Product Support 203-349-2798
fi gure 3B
Page 13
10.2. TREATMENT LOCATIONS
Knee
Shoulder
Figures 4 and 5 depict examples of device
placement on two treatment locations. Figure
4A and 4B illustrates using the
one applicator on the shoulder and knee. Figure
5A and 5B illustrates using the sam Device with
two applicators on the shoulder and knee. When
determining treatment location, consider that
the maximum diathermic eff ect will occur directly
under the applicator face; therefore, placing
the applicator near or directly over the target
area while following all warning and cautionary
instructions is advised.
Note: These fi gures are examples and are not
intended to be the suggested or only
allowable applicator confi gurations for those
body locations.
Warning: Do Not apply directly over a bone that is
near the skin surface.
sam Device with
fi gure 4A: Single Shoulder Application
10.3. ONE OR TWO APPLICATORS:
The sam Device may be used with one or two
applicators simultaneously. The decision to use
one or two applicators is dependent on the
size and anatomical area of treatment. Using
two applicators allows a larger area of tissue to
receive ultrasound treatment. For example, large
anatomical regions, such as the shoulder could
benefi t from two applicators, whereas smaller
treatment areas such as the forearm may only
require one.
10.3.1. SINGLE-APPLICATOR MODE
Connect the power controller wire to a single
applicator by inserting the power controller wire
jack into the matching cavity at the base of the
applicator. The port for the power controller wire is
described as ‘Applicator connection’ on the Power
Controller drawing shown in Figure 2, page 10.
fi gure 4B: Single knee Application
fi gure 5A: Dual Shoulder Application
fi gure 5B: Dual Knee Application
14 Product Support 203-349-2798
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10.3.2. DUAL-APPLICATOR MODE
The Y-adapter (optional) may be used to power two Applicators simultaneously. As
shown in Figure 8, connect the Y-adapter directly to the Power Controller wire and then
connect each Applicator to a wire jack at the other end of the Y-adapter.
When using two
simultaneously, the
their footprints do not overlap.
Caution: DO NOT overlap
Caution: DO NOT use the Y-adapter when using only one applicator for treatment.
Caution: Do NOT attach more than one Y-adapter to the sam Device.
Note: If two applicators will be used, two
each applicator) and the Y-adapter must be used for the treatment.
sam Applicators and two sam Ultrasound Coupling Bandages
sam Ultrasound Coupling Bandages should be positioned so that
sam Ultrasound Coupling Bandages (Figure 6).
sam Ultrasound Coupling Bandages (one for
fi gure 6: NO Bandage Overlap
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11. Application Instructions
11.1. CHECK DEVICE CHARGE
A. To prevent accidental activation during
shipping, the device will arrive to the user
in the ‘locked’ position. To unlock the
device, slide the Lock Switch on the
Power Controller ‘up’ into the ‘unlocked’
position (Figure 7A).
B. Check to make sure the Power Controller
holds enough charge to provide the
desired duration of treatment. Press
the Toggle Button on the
Controller to view the battery indicator
lights (Figure 7B). The lights will illuminate
to show how much battery life is remaining
in the device. If the device is not fully
charged it may not be able to deliver
treatment for 4 hours. The device will only
permit the user to set a treatment duration
for which the battery charge is capable
of fulfi lling.
sam Power
sam
Lock
Switch
i. To check the treatment duration for
which the battery charge is capable of
fulfi lling, simply continue to press the
Toggle Button sequentially to view all
timer settings allowed by the current
battery charge. See section 9 for
charging instructions.
16 Product Support 203-349-2798
fi gure 7A: Check Device Charge
Toggle
Button
fi gure 7B: Check Device Charge
Page 16
11.2. CONNECT APPLICATOR TO POWER CONTROLLER
HRS
DONE
%
20
100
80
60
40
3
2
1
3.5
4
2.5
1.5
Rotate Clockwise
45
* If using 2 applicators: fi rst connect the Y-adapter directly to the power controller
wire jack and then connect each applicator to a wire jack at the other end of the
Y-adapter (Figure 8*).
A. Insert the power controller wire into the matching cavity at the base of the
applicator at a 45 degree angle (Figure 8A).
B. Gently twist the wire jack clockwise until the applicator edge is fl ush with the
wire jack (Figure 8B).
fi gure 8*: Connecting Y-Adapter
fi gure 8B: Gently twist to Lock
fi gure 8A: Insert power controller wire at 450 angle
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11.3. ATTACH APPLICATOR TO BANDAGE
A. Remove the circular seal from the top of
the bandage to reveal the coupling media
within the gel cup (Figure 9A).
B. Attach the applicator, face down, into the
coupling media (Figure 9B).
C. Firmly press the applicator down onto the
center of the gel cup until a clicking noise
is heard or clicking sensation is felt
(Figure 9C).
If using dual applicators, repeat these steps with
the second applicator and the second bandage.
Note: When the applicator is pressed down onto
the gel cup, do not be concerned if coupling
media fl ows out the edges of the gel cup.
Wipe any excess coupling media away with
a tissue or towel.
Note: Ensure the applicator is fully attached to
the bandage.
fi gure 9A: Removing Foil Seal
fi gure 9B: Attach Applicator
fi gure 9C: Press Applicator Down
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11.4. APPLY ULTRASOUND
Knee
COUPLING BANDAGE TO
TREATMENT LOCATION
A. Hold the applicator so the bottom of the
bandage faces up. Remove the paper liner
from the back of the bandage, revealing
the bandage adhesive (Figure 10A).
i. The circular seal should peel off the
bottom of the gel cup along with the
paper bandage liner. If it does not peel
with the paper, be sure to peel away
the circular seal so the coupling media
is completely uncovered.
ii. Add more
as needed.
B. Turn the bandage over and adhere the
bandage to the desired treatment location
(Figure 10B).
sam Coupling Media
fi gure 10A: Removing Paper Liner
i. The
If using dual applicators, repeat these steps to
adhere the second bandage and applicator to the
second treatment site.
Note: When applying bandages, both sides of
the ultrasound coupling media should be
uncovered. One side should be in contact
with the skin. The other side should be in
contact with the face of the applicator.
sam Coupling Media must be in
direct contact with the skin.
fi gure 10B: Adhere Bandage to Site
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11.5. TURN THE DEVICE ‘ON’
Power Button
1
2.5
1.5
HRS
DONE
%
20
100
80
60
40
3
2
1
3.5
4
2.5
1.5
A. Check to make sure the Lock Switch is in
the ‘unlocked’ position (Figure 11A).
B. Press and hold the Power Button on
the
sam Power Controller for at least 1
second to turn the device ‘ON’ (Figure 11B).
i. As confi rmation that the device is ‘ON’,
the LEDs on the
will illuminate blue (treatment timer and
indicator LEDs) and the indicator LED
on the applicator will illuminate blue.
ii. The battery indicator LEDs will remain
‘ON’ for about 4 seconds after turning
‘ON’ the device.
iii. The treatment timer LEDs and blue
indicator LEDs (power controller and
applicator) will remain ‘ON’ for the
duration of treatment.
C. Press the Toggle Button to select 1, 2, 3 or
4 hour treatment duration (as allowed by
current battery charge) (Figure 11C).
i. If the Toggle Button is pressed up to
the 4 hour setting and a decreased
treatment time is desired, pressing it
again will return the treatment timer to
the 1 hour setting.
sam Power Controller
Toggle
Button
Lock
Switch
fi gure 11A: Slide to Unlocked Position
fi gure 11B: Press Power Button
Toggle
Button
Lock
Switch
fi gure 11C: Select Duration
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11.6. PREVENT UNINTENTIONAL SHUTOFF
Once satisfi ed with the treatment settings, the
settings may be locked to prevent unintentional
shutoff during treatment by sliding the Lock Switch
down into the ‘locked’ position as indicated by
the symbols on the
Figure 11A). In this state the settings cannot be
changed until the Lock Switch is moved back to the
‘unlocked’ position.
Note: The system is not required to be locked in
order to operate. Always be aware of how
to disable a locked device. Always notify the
patient if their device is locked.
sam Power Controller (see
11.7. TREATMENT DELIVERY
Treatment will be delivered for the duration set by
the user. The treatment timer LEDs will count down
in 30 minute increments as treatment progresses.
Upon completion, the device will automatically shut
off and the ‘treatment complete’ LED will illuminate
for approximately 8 hours before turning off . See
section 12 for how to manually power ‘OFF’
the device.
Warning: If the
Warning: ALWAYS instruct the patient to alert the practitioner in the event of discomfort
Warning: As an additional safety measure, ALWAYS instruct the patient how to turn off
Warning: ALWAYS keep the
sam Lock Switch is in the locked position, the sam Power Button will
not turn off the device until the sam Lock Switch is placed into the
unlocked position.
during treatment.
the
sam Device and remove the sam Applicator in the event of discomfort
or emergency.
sam Power Controller within easy reach so that power may
be ceased at any time.
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12. Device Power Down and Removal
MODEL
AT-12
Pull Tab
12.1. POWER OFF THE POWER CONTROLLER
Move the Lock Switch up to the ‘unlocked position’ (if locked) then press and hold the
Power Button on the
‘OFF’ (See Figure 11B for device diagram).
12.2. REMOVE DEVICE FROM SKIN
A. Remove the bandage(s) from the skin.
B. Remove the applicator from the sam Ultrasound Coupling Bandage by pulling
the tab on the side of the gel cup. This unlocks the cup from the applicator
(See Figure 12).
sam Power Controller for at least 1 second to turn the device
C. Throw away the
Warning: NEVER use a sam Ultrasound Coupling Bandage for more than one use.
Misuse of sam Ultrasound Coupling Bandages or use for more than the
intended treatment duration MAY RESULT IN BURN OR REPEATED SHUTOFF
of the applicator.
sam Bandages.
12.3. CLEAN THE APPLICATORS
Clean any residual ultrasound coupling media off of the applicator and off of the skin.
See section 14 for ‘Cleaning and Maintenance’ details.
12.4. RECHARGE THE DEVICE
Connect the sam Power Controller to the sam Electrical Charger for recharging. Prior
to the next use, allow up to 6 hours to recharge the battery to 100% charge. See section
9 for charging instructions.
fi gure 12: Removing Applicator
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13. Modes of Operation
13.1. ON (UNLOCKED) MODE
To turn the device ‘ON’, fi rst ensure the Lock Switch is in the unlocked position as
indicated by the unlocked symbol on the
hold the Power Button for at least 1 second. Press the Toggle Button on the right side
of the sam Power Controller Module to set the treatment duration. The treatment
duration may be set for 1, 2, 3 or 4 hours. The battery indicator LED and treatment timer
LED will be displayed on the control panel (see section 8: LED Display). The applicator
indicator LED will be displayed on each attached applicator (See Figure 2, page 10).
Each connected applicator will emit ultrasound energy immediately upon the
Power Controller Module entering the ‘ON’ mode of operation. The sam Applicator will
emit ultrasonic energy whether the device is locked or unlocked (locking is optional). A
powered sam Applicator will always emit ultrasonic energy unless it enters the sam
Sensing Mode or the treatment duration concludes.
13.2. ON (LOCKED) MODE
Once the device is powered ‘ON’, the user may lock the control panel settings by
sliding the Lock Switch on the sam Power Controller Module to the ‘locked position’ as
indicated by the lock symbol on the sam Power Controller Module. This will prevent the
device from unintentional shutoff during treatment. While locked, the Power Button and
the Toggle Button cannot be modifi ed. The sam Applicator will emit ultrasound whether
the device is locked or unlocked. To change the treatment duration or turn the power
off , simply slide the Lock Switch to the ‘unlocked position’ as indicated by the symbols
on the
sam Power Controller Module then press the desired user button.
Warning: If the Lock Switch is in the locked position, the Power Button will not turn off
the device until the Lock Switch is placed into the unlocked position. Locking
the treatment settings is not required.
sam Power Controller Module. Press and
sam
13.3. OFF MODE
When the device is ‘OFF’, the LEDs on the applicator will not be illuminated, the LEDs
on the
sam Power Controller Module will not be illuminated, and no ultrasound energy
will emanate from the device. Always turn the device ‘OFF’ when not in use or if pain or
uncomfortable heating is indicated by the patient.
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13.4. SAM SENSING MODE
In the event that the treatment site underneath the applicator reaches the temperature
threshold, the applicator will pause ultrasound output and vibrate once with a red LED
notifi cation to signify that the device has begun a cooling or rest cycle.
will automatically resume treatment with a blue LED notifi cation after the site
has cooled.
Warning: Should the patient ever report discomfort or a painful sensation from the site
under the
Caution: At no time during treatment should the applicator be covered by thick
insulating material such as a coat, blanket or sports wrap. This may cause
sam Applicator, the applicator should be removed immediately.
sam Applicator
sam to disable and remain disabled throughout the therapy session.
13.5. END OF TREATMENT MODE
At the end of treatment, an amber-colored “Treatment Complete” LED will illuminate on
the sam Power Controller Module and all other displays (battery indicator, treatment
timer, indicator LED, and applicator LEDs) will be inactive. All ultrasound emissions from
the applicator will cease. The “Treatment Complete” LED will remain illuminated for
approximately 8 hours after completion of therapy, at which point it will time out and
turn off . To set the
to the unlocked position and assess whether the
sam Device for a new treatment, remember to move the lock switch
sam Device requires recharging.
14. Cleaning and Maintenance
The exterior of the sam Power Controller and the applicator surfaces may be cleaned
with a soft cloth, tissue, or towel and one of the following cleaning agents: mild
detergent and water or disinfecting medical wipes.
Caution: Properly clean the applicator between treatments.
Caution: The device is not waterproof. Do not apply a direct stream of liquid onto the
device, submerge the device, or allow any liquid to pool on the surface of
the device.
Caution: DO NOT USE: Phenolic-based disinfectants, quaternary ammonium, chlorine-
based disinfectants, solvent-based cleaners, or abrasive materials. Doing so
may damage the plastic housing and void the warranty.
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15. Storage & Operating Conditions
15.1. STORAGE
Store the sam Device in the following conditions:
Temperature: 557 °C;
Humidity: 1080%;
Atmospheric pressure range: 7001060 hPa
Store the sam Ultrasound Coupling Bandages in the following conditions:
Temperature: 530 °C;
Humidity: 1080%;
Atmospheric pressure range: 7001060 hPa
15.2. OPERATION
Only operate the sam Device in the following conditions:
Temperature: 144 °C;
Humidity: 1080%;
Atmospheric pressure range: 7001060 hPa
Caution: Do not keep the device in extreme hot or cold temperatures (above 50°C or
below 0°C). Do not leave the
the device in direct sunlight for extended periods. UV light may damage or
discolor the device.
sam Device in a hot or freezing car. Do not leave
16. Disposal of Waste Products
sam Ultrasound Coupling Bandages are one time use and may be disposed of in
regular sanitation trash. No special disposal procedures are necessary.
Old, damaged or expired sam Power Controller Modules and applicators should be
recycled or returned to the manufacturer for proper disposal.
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17. Appendix
A. SYMBOLS
Consult User Manual/Instructions for Use
Manufacturer/Date of Manufacture
Lithium-ion battery inside
Li-ion
Class BF Applied Part
Do not use if package is damaged
Do not reuse
Non-ionizing radiation
Separate collection for electrical and electronic equipment.
be disposed of in unsorted municipal waste.
Caution, consult accompanying documents
Diverging beam
Continuous wave (CW)
Watts, ultrasonic power
W
Frequency in megahertz
MHz
Eff ective radiating area
ERA
Beam non uniformity ratio
BNR
Use by date
Temperature limits
Humidity limitation
SN
Serial number
Catalogue/Reorder Number
LOT
Lot number
Must not
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B. SPECIFICATIONS
The sam Device does not contain microprocessor or software
Maximum Acoustic 0.65 W +20% per transducer
Power Output 1.3 W +20% for 2 transducers
Maximum Intensity 0.132 W/cm
Frequency 3 MHz
Duty Cycle 100% - continuous wave
Beam Form Wide Beam – 5 degree diverging lens
Individual Transducer Dimension 5 cm
BNR <5:1
ERA 6 cm
Maximum Treatment Duration 4 hours
2
+20%
+
20%
2
emitting surface area (circular)
2
+
20 %
Other Electrical Ratings for the
Electrical Charger (Model GS2U-006-050-A)
sam Device Components
Input Voltage 100240 V, 5060 Hz
Input Current 0.2 A
Output Voltage 5 V DC
Output Current 1.2 A
Max Output Power 6 W
Power Controller
Output Voltage 3.7 V DC +10%
Max Output Amperes 700 mA
Battery Protection Max Current: 2 Amps
Max Voltage: 4.2 V
Min Voltage: 3.1 V
Cable Voltage Rating 300 V
Cable 20°C Resistance: 94/km
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Applicator
Input Voltage: 3.7 V DC +10%
Ultrasound Frequency: 3 MHz +20%
Ultrasonic Output Power: 1 Transducer: 0.65 W +20%
2 Transducers Together: 1.3 W +20%
Max Input Current: 400 mA
Y-Adapter
Voltage Rating 300 V
20°C Resistance 94/km
C. NOTICE OF COMPLIANCE, CALIBRATION AND
OPERATIONAL PERIOD
The sam Device meets performance standards under 21 C.F.R. § 1050.10 PERFORMANCE STANDARDS FOR SONIC, INFRASONIC, AND ULTRASONIC RADIATIONEMITTING PRODUCTS. The sam Device meets IEC 606011, 3 ed. (2012); IEC 60601-
12, 3 ed. (2007); Medical Electrical Equipment, General Requirements for Safety;
Electromagnetic Compatibility. The sam Device is calibrated to provide 3 MHz +20%
ultrasound diathermy at 0.65 W +20% per ultrasound applicator.
Operational Period:
The
sam Power Controller Module is intended to maintain calibration for up to 300
charging cycles and each ultrasound applicator is intended to withstand 1500 hours
of run time, after which the system should be recycled or returned to ZetrOZ, Inc. for
proper disposal.
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D. TECHNICAL INFORMATION
fi gure A. Ultrasound Field Scan Across Applicator Face
fi gure B. Ultrasound Field Scan Away From the Applicator Face
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E. ELECTRICAL IMMUNITY AND EMISSIONS
The following components of the sam Ultrasonic Diathermy Device are
compliant with the requirements of IEC 6060112 ed 3.0 (200703):
sam Model 12
Cable Length
AT-12 : Ultrasound Applicators
UB-12: Ultrasound Coupling Bandages
PMC-12: Power Controller Module 48 inches +1.2
CT-12: Electrical Charger 60 inches +2.0
YB-12: Y-branch Adapter 8 inches +.6 x 2
Guidance and Manufacturer’s Declaration – Emissions
Emissions Test Compliance Electromagnetic Environment – Guidance
RF Emissions Group 1 The
CISPR 11 function. Therefore, its RF emissions are very low
and are not likely to cause any interference in
nearby electronic equipment.
RF Emissions Class B The
CISPR 11 including domestic, and those directly connected
Harmonics Class A
IEC 6100032
Flicker
IEC 6100033
sam uses RF energy only for its internal
sam is suitable for use in all establishments,
to the public low-voltage power supply network
that supplies buildings used for domestic
purposes.
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Guidance and Manufacturer’s Declaration – Immunity All
ME Equipment and ME Systems
The sam is intended for use in the electromagnetic environment
specifi ed below. The customer or user of the sam should ensure
that it is used in such an environment.
Immunity Test IEC 60601 Compliance Electromagnetic
Test Level Level Environment - Guidance
ESD
IEC 6100042 +8kV Air
EFT 2kV Mains
IEC 61000044 +1kV IOs
or hospital environment.
Surge
IEC 6100045 +2kV Common Common NA that of a typical commercial or
(no ground) hospital environment.
Voltage >95% Dip for >95% Dip for Mains power quality should be
Dips/Dropout 0.5 Cycle 0.5 Cycle that of a typical commercial or
IEC 61000411 60% Dip for 60% Dip hospital environment. If the user
5 Cycles 5 Cycles of the
30% Dip for 30% Dip for operation during power mains
25 Cycles 25 Cycles interruptions, it is recommended
>95% Dip for >95% Dip for that the
5 Seconds 5 Seconds an uninterruptible power supply
or battery.
Power 3A/m 3A/m Power frequency magnetic fi elds
Frequency should be that of a typical
5060Hz commercial or hospital
Magnetic Field environment.
IEC 6100048
+
6kV Contact +6kV Contact Floors should be wood, concrete
+
8kV Air or ceramic tile. If fl oors are
synthetic, the r/h should be at
least 30%.
+
2kV Mains Mains power quality should be
+
1kV IOs that of a typical commercial
+
1kV Diff erential +1kV Diff erential Mains power quality should be
sam requires continued
sam be powered from
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Guidance and Manufacturer’s Declaration – Immunity
The sam is intended for use in the electromagnetic environment
specifi ed below. The customer or user of the sam should ensure
that it is used in such an environment.
Immunity Test IEC 60601 Compliance Electromagnetic
Test Level Level Environment - Guidance
Portable and mobile communications
equipment should be separated from
the
sam by no less than the distances
calculated/listed below:
Conducted RF 3 Vrms (V1) = 3 Vrms D = (3.5V1)(Sqrt P)
IEC 6100046 150 kHz to 150 kHz to 80 MHz
80 MHz
Radiated RF 3V/m D = (3.5Eq)(Sqrt P)
IEC 6100043 80 MHz to (E1) = 3 V/m 80 to 800 MHz
2.5 GHz
D=7E1)(Sqet P)
800 MHz to 2.5 GHz
Where P is the max power in watts and D
is the recommended separation distance
in meters.
Field strength from fi xed transmitters,
as determined by an electromagnetic
site survey, should be less than the
compliance levels (V1 and E1).
Interference may occur in the vicinity of
equipment containing a transmitter.
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Recommended Separation Distances between portable and
mobile RF Communications equipment and the sam ME Equipment and
ME Systems that are NOT Life-supporting
The sam is intended for use in the electromagnetic environment in which radiated
disturbances are controlled. The customer or user of the
electromagnetic interference by maintaining a minimum distance between portable
and mobile RF Communications Equipment and the
according to the maximum output power of the communications equipment.
Max Output Separation (m) Separation (m) Separation (m)
Power (Watts) 150kHz to 80MHz 80 to 800MHz 800MHz to 2.5GHz
D=3.5V1)(Sqrt P) D=3.5E1)(Sqrt P) D=3.5E1)(Sqrt P)
0.01 0.11667 0.11667 0.23333
0.1 0.36894 0.36894 0.73785
1.0 1.1667 1.1667 2.3333
10.0 3.6894 3.6894 7.3785
100.0 11.667 11.667 23.333
sam can help prevent
sam as recommended below,
F. WARRANTY
ZetrOZ, Inc. off ers a 1-year manufacturer’s warranty for the sam Device. If the sam
Device fails due to defects in material or workmanship, ZetrOZ, Inc., at its discretion, will:
1. REPAIR the
2. REPLACE the sam Device with another sam Device
THIS LIMITED WARRANTY AND ANY IMPLIED WARRANTIES THAT MAY EXIST UNDER
STATE LAW APPLY ONLY TO THE ORIGINAL PURCHASER OF THE
NONTRANSFERABLE.
Extent of Limited Warranty
This limited warranty does not cover damages due to external causes, including,
without limitation, accident, usage not in accordance with product instructions, misuse,
neglect, alteration or repair.
sam Device OR
sam DEVICE AND ARE
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G. TROUBLESHOOTING
Question or Problem Solution
1. How to determine if As confi rmation that the device is delivering ultrasound,
the device is delivering the LEDs on the Power Controller will illuminate blue
treatment (treatment timer and indicator LEDs) and the indicator LED
on the applicator will illuminate blue. See section 8 on
LED Display.
2. The device isn’t Ensure the power controller lock switch is in the UNLOCKED
turning ON and the position. If the device still fails to power ONOFF or toggle
buttons aren’t working treatment duration, contact the manufacturer with serial
and model number details.
3. The indicator LED on Ensure that the applicator is fully connected to the power
the Applicator does not controller wire jack and/or the Y-adapter wire jack. If
illuminate when the recently in
device is turned ON has had time to reach normal operating temperature and
the indicator LED on the applicator has turned from red
back to blue. If the applicator LED still fails to illuminate
blue, contact the manufacturer with serial and model
number details.
sam Sensing Mode, ensure that the applicator
4. How to observe the The Battery Indicator display can only be viewed when
Battery level during the device is powered ON or OFF by pressing the Power
treatment Button, or when the Toggle Button is pressed. (See section
11.1) The lights remain illuminated for approximately 4
seconds after the device is turned ON or OFF. The Battery
Indicator LEDs do not remain illuminated during treatment.
The treatment duration is indicated by the blue treatment
timer LEDs (See section 8 on LED display).
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G. TROUBLESHOOTING
Question or Problem Solution
5. The Applicator is Turn off the device. Remove the sam Ultrasound Coupling
not staying secured Bandage from the applicator. Replace with new
during treatment Ultrasound Coupling Bandage. See section 11.3 for gel cup
application instructions.
sam
6. The Applicators are The device has entered ‘
vibrating and red 13.4) Each sam Applicator is equipped with closed-loop
continuous temperature monitoring which maintains
treatment site temperatures below 44°C during normal
operation. In the event that the treatment site underneath
the applicator reaches the temperature threshold, the
applicator will pause ultrasound output and vibrate once
with a red LED notifi cation that the device has begun
a cooling or rest cycle.
treatment with a blue LED notifi cation after the site has
cooled. Caution: At no time during treatment should the
applicator be covered by thick insulating material such as
a coat, blanket or sports wrap. This may cause
disable and remain disabled throughout the
therapy session.
sam Sensing Mode’ (See section
sam will automatically resume
sam to
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sam
Manufactured by ZetrOZ, Inc.
56 Quarry Road
Trumbull, CT 06611
USA
Toll Free Tel 18882029831
USA User Manual (OM12) — LL253501 Rev.B
Published 06042014
0086
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