ChoiceMMed MDTS100 User manual

Electronic Pulse Stimulator
INSTRUCTION MANUAL
MDTS100
Version 3.0

CONTENT
1 Box Contents....................................................................................................................................................1
2 Introduction.......................................................................................................................................................1
3 Intended use.....................................................................................................................................................1
4 Indications for use ............................................................................................................................................1
5 Contraindication................................................................................................................................................1
6 Features of MDTS100 ......................................................................................................................................1
7 Safety Warnings ...............................................................................................................................................2
8 Specication .....................................................................................................................................................3
9 Procedures include the following parameters:..................................................................................................4
10 How the Device Works ...................................................................................................................................9
11 Understanding Your Unit...............................................................................................................................10
12 Operating Instructions ..................................................................................................................................10
13 Accessories ..................................................................................................................................................12
14 Electrode Pads User Guide..........................................................................................................................13
15 Quality Assurance Tests ...............................................................................................................................13
16 Cleaning and Measurement .........................................................................................................................13
17 Position for Use ............................................................................................................................................14
18 Troubleshooting............................................................................................................................................14
19 Symbols........................................................................................................................................................15
20 Compliance Information for EMC Test..........................................................................................................16

1
1 Box Contents
ChoiceMMed Electronic Pulse Stimulator MDTS100 *1
Lead Wires with Pin Connection *2
AAA Batteries *2
Electrode Pads *4
User Guide *1
2 Introduction
The MDTS100 Electronic Pulse Stimulator device has seven stimulation modes: Mode1, Mode2,
Mode 3, Mode 4, Mode 5, Mode 6, Mode 7. These stimulation modes can be selected by
pressing the MODE button on the front of the unit.
The MDTS100 comes with 2 independent output channels (A&B). Each channel comes with
an electrode wire & two electrode pads. Users can choose between the two output channels
by pressing the CHA button. Channel A&B are selected by default. Pressing the buttons
will decrease & increase the intensity of stimulation. LCD screen display the left remaining
stimulation time in the lower left corner. The default time is 20 minutes.
3 Intended use
The MDTS100 Electronic Pulse Stimulator is intended for at home use in delivering electric
pulses to tired and sore muscles. These pulses to tired and generated by the device & delivered
through electrode pads placed on the targeted muscles.
4 Indications for use
The Electronic Pulse Stimulator MDTS100 is to be used for temporary relief of pain associated
with sore and aching muscles in the shoulder, waist, back, upper extremities (arm), and lower
extremities (leg) due to strain from exercise or normal household and work activities.
5 Contraindication
Consult your physician before purchasing or using this device if you have one of the following
conditions:
• Acute disease
• Malignant tumor
• Infective disease (i.e. HIV/AIDS, Pneumonia)
• Pregnant
• Heart disease
• High fever
• Abnormal blood pressure
• Lack of skin sensation
• Abnormal skin condition
• Any condition requiring the active supervision of a physician
6 Features of MDTS100
• Liquid Crystal Display (LCD) Screen
• 2 Independent Output Channels
• 7 Stimulation Modes (Mode 1, Mode 2, Mode 3, Mode 4, Mode 5, Mode 6 and Mode 7)

2
• 10 Levels of intensity
• 8 Positions (LEG, SOLE, FOOT, BACK, SHOULDER, HAND, JOINT and WAIST)
• 20 Minutes Timer
7 Safety Warnings
DANGER
• Do not use this device if you have an implanted debrillator or implanted metallic devices,
such as a pacemaker. Such use could cause electrical shock, burns, electrical interference
or death.
• Don't use the device if you use a high frequency surgical ME EQUIPMENT simultaneously.
Such use may result in burns and possible damage to the device.
• Operation in close proximity (e.g. 1m) to a shortwave or microwave therapy ME
EQUIPMENT may produce instability in the device output.
• The application of electrodes near the thorax may increase the risk of cardiac brillation.
WARNING
• Use of accessories and cables other than those specied or provided by the manufacturer
of this equipment could result in increased electromagnetic emissions or decreased
electromagnetic immunity of this equipment and result in improper operation.
• Portable RF communications equipment (including peripherals such as antenna cables
and external antennas) should be used no closer than 30 cm (12 inches) to any part of the
ME EQUIPMENT, including cables specied by the manufacturer. Otherwise, degradation
of the performance of this equipment could result.
• Use of this equipment adjacent to or stacked with other equipment should be avoided
because it could result in improper operation. If such use is necessary, this equipment and
the other equipment should be observed to verify that they are operating normally.
NOTICE
• Do not use this device while driving or sleeping.
• Do not use this device in high humidity areas such as a bathroom.
• Keep the device away from wet, high temperature and direct-sunlight place.
• Keep this device out of reach of children.
• Stop using this device and consult your physician immediately if you feel pain, discomfort,
dizziness or nausea.
• Do not attempt to move the electrode pads while the device is ON or operating.
• Any electrodes that have current densities exceeding 2mA/cm2 may require special
attention of the operator.
• Do not use the device around the heart, on the head, mouth, genitals or blemished skin
areas, on the front of the neck, or from electrodes placed on the chest and the upper back
or crossing over the heart.
• When the device delivers an output of more than 10mA or 10V into a load resistance of
1000Ω, the device will have an indication that the A&B channels font ashes on the display
screen.
Do not apply stimulation of this device in the following conditions:
1. Across the chest-the introduction of electrical current into the chest may cause rhythm
disturbances to the heart, which could be lethal.
2. Over painful areas. Consult your physician before using this device if you have painful
areas.
3. Over open wounds, rashes, or swollen, red, infected, or inamed areas or skin eruptions
(e.g. phlebitis, thrombophlebitis, varicose veins). Apply stimulation only to normal, intact,

3
clean and healthy skin.
4. In the presence of electronic monitoring equipment (e.g., cardiac monitors, ECG alarms).
The electronic monitoring equipment may not operate properly when the electrical pulse
stimulator is in use.
5. While operating machinery, or during any activity in which electrical stimulation can put
you at risk of injury.
6. On children.
7. Over your neck because this could cause severe muscle spasms resulting in closure of
your airway, difcultly in breathing, or adverse effects on heart rhythm or blood pressure.
8. Over, or in proximity to, cancerous lesion.
9. When the patient is in the bath or shower.
Be aware of the following:
1. Consult your physician before using this device. The stimulation with the device may: i.
cause lethal rhythm disturbances to the heart in susceptible individuals, and, ii. disrupt the
healing process after a recent surgical procedure.
2. The device is not effective for pain of central origin (i.e. appendicitis, Hepatitis), including
headache.
3. The device is not a substitute for pain medications and other pain management therapies.
4. The device has no curative value.
5. The device is a symptomatic treatment and, as such, suppresses the sensation of pain
that would otherwise serve as a protective mechanism.
6. The long-term effects of electrical stimulation are unknown.
7. The user may experience skin irritation, burns or hypersensitivity due to the electrical
stimulation or electrical conductive medium (gel).
8. If the user has suspected or diagnosed epilepsy, the user should follow precautions
recommended by his or her physician.
9. Use caution if the user had a tendency to bleed internally, such as following an injury or
fracture.
10. Use caution if stimulation is applied over the menstruating uterus.
11. Use caution if stimulation is applied over areas of skin that lack normal sensation
12. Stop using the device if the device does not provide pain relief
13. Use this device only with the wires, electrodes, and accessories that the manufacturer
recommends
14. Patient is intended operator.
15. Effectiveness is highly dependent upon patient selection by a practitioner qualied in the
management of pain patients.
16. Science the effects of stimulation of the brain are unknown, stimulation should not be
applied across the head, and electrodes should not be placed on opposite sides of the
head.
17. Do not use the stimulator near an MRI environment.
Medical Electrical Equipment needs special precautions regarding electromagnetic compatibility
(EMC) and needs to be installed and put into service according to the EMC information
provided. Portable and mobile radio frequency (RF) communication equipment can affect
Medical Electrical Equipment.
8 Specication
Dimensions (in.) [W x H x D]: 2.17x 5.12x0.87
LCD Display (in.): 1.46x1.46

4
Size of electrodes (in.): 1.57×1.57
Weight: 2.2oz (Battery Excluded)
Power: DC 3V, 2 AAA batteries
Life of Pads: Up to 80 Uses
Power Requirements
Two AAA Alkaline Batteries
Battery Life: Two AAA 1.5V, 800mAh alkaline batteries could be continuously operated as long
as 20h.
Environment Condition
Environmental condition for transportable & storage
Temperature Range: -13 ℉~158 ℉(-25℃~70℃)
Humidity: ≤93%
Atmosphere Pressure: 700hPa~1060hPa
Environment condition for operation
Temperature Range: 41 ℉~104 ℉(5℃~40℃)
Humidity: 15% to 93% RH
Atmosphere Pressure: 700hPa~1060hPa
Technical Specication
Power Source: 3V battery
Number of output modes: 7
Number of alternating output channels: 2
Timer Range (minutes): 20 minutes
Dimensions (in.) [W x H x D]: 2.17x 5.12x0.87
Waveform: monophasic
Shape: monophasic square wave
Maximum Output Voltage(±20%): 150V@500Ω; 60V @2kΩ; 165V@10kΩ
Maximum Output Current(±20%): 300mA @500Ω; 80mA @2kΩ; 16.5mA @10kΩ
Duration of primary (depolarizing) phase: 0µsec
Pulse Duration: 50~140µsec
Frequency: 0.9Hz~82Hz
Net charge: 42µC@500Ω
Maximum phase charge: 42µC@500Ω
Maximum current density: 3.3mA/cm2
Maximum average current: 2.8 mA
Maximum average power density: 0.02 W/cm2
Burst Mode (Pulses per burst): 197
(Burst per second): 0.185
(Burst duration): 2.4s
(Duty Cycle): 0.44
ON TIME: ≤1second
OFF TIME: ≤1second
9 procedures include the following parameters:
Procedure contains the master pulse and the sub pulse, the working time of master pulse
consists of several sub pulses while the sub pulse consists of several single pulses. Without
special instruction in procedure: single pulse width is 140µS; the therapy time is 20 minutes.
Mode 1
• Frequency : 35Hz
• Pulse Width: 50-140µS

5
• The Maximum amplitude (500Ωload):150V
Output waveforms at loads of 500Ω Output waveforms at loads of 2kΩ
Output waveforms at loads of 10kΩ Output waveforms Pulse burst (500Ω)
Mode 2
• Frequency : 6.25Hz/0.9Hz/2.25Hz
• Pulse Width: 140µS
• he Maximum amplitude (500Ωload):150V
Second procedures consist of three pulses with different frequency (6.25Hz/0.9Hz/2.25Hz)
Output waveforms at loads of 500Ω Output waveforms at loads of 2kΩ
Output waveforms at loads of 10kΩ Output waveforms Pulse burst (500Ω)

6
Mode 3
• Frequency : 35Hz
• Pulse Width: 50-140µS
• the Maximum amplitude (500Ωload):150V
Output waveforms at loads of 500Ω Output waveforms at loads of 2kΩ
Output waveforms at loads of 10kΩ Output waveforms Pulse burst (500Ω)
Mode 4
• Frequency : 35Hz
• Pulse Width: 140µS
• The Maximum amplitude (500Ωload):120V
Output waveforms at loads of 500Ω Output waveforms at loads of 2kΩ
Output waveforms at loads of 10kΩ Output waveforms Pulse burst (500Ω)

7
Mode 5
• Frequency : 35Hz
• Pulse Width: 140µS
• The Maximum amplitude (500Ωload):120V
Output waveforms at loads of 500Ω Output waveforms at loads of 2kΩ
Output waveforms at loads of 10kΩ Output waveforms Pulse burst (500Ω)
Mode 6
• Frequency : 82Hz
• Pulse Width: 140µS
• The Maximum amplitude (500Ωload):80V

8
Output waveforms at loads of 500Ω Output waveforms at loads of 2kΩ
Output waveforms at loads of 10kΩ Output waveforms Pulse burst (500Ω)
Mode 7
• Frequency : 35Hz
• Pulse Width: 140µS
• The Maximum amplitude (500Ωload):120V
Output waveforms at loads of 500Ω Output waveforms at loads of 2kΩ
Output waveforms at loads of 10kΩ Output waveforms Pulse burst (500Ω)

9
Description of each mode:
Mode Frequency
(Hz)
Pulse
Width
(µs)
Max
amplitude (V)
@500Ωload
Output
Mode Type of Pain Therapy deliver
Mode 1 35 50-140 150 Cycle&
Modulated
Acute&
Chronic Pain
Massage-Like
feeling
Mode 2
6.25
/0.9
/2.25
140 150 Cycle&
Modulated Acute Pain
Variable tingling and
pulsing sensation
(sensation should
appear to come in
waves)
Mode 3 35 50-140 150 Cycle&
Modulated Chronic Pain
Variable
comfortable pulsing
sensation(sensation
should appear to
come in waves)
Mode 4 35 140 120 Constant&
Modulated Chronic Pain
Constant
comfortable pulsing
sensation(sensation
should appear to
come in waves)
Mode 5 35 140 120 Cycle&
Modulated
Acute&
Chronic Pain
Variable stimulation
sensation(sensation
should appear to
come in waves)
Mode 6 82 140 80 Constant&
Modulated
Acute&
Chronic Pain
Constant
comfortable rubbing
sensation
Mode 7 35 140 120 Cycle&
Modulated Chronic Pain
Variable pulsing
and pumping
action(sensation
should appear to
come in waves)
10 How the Device Works
The MDTS100 device generates small pulses of electrical current. It delivers these pulses to the
user’s skin through adhesive electrode pads such that the underlying nerves are activated and
the pain associated with sore and aching muscles is temporarily relieved.

10
11 Understanding Your Unit
12 Operating Instructions
The following steps are used to guide the device operation. The details about each step are
listed in the following chart.
Step 1 Insert 2 AAA batteries into the device
Step 2 Connect the electrode pads to the wires and then connect the wires to the device
Step 3 Put the electrode pads on the stimulation-needed body area
Clean your skin before each use. Make sure your skin is clean, dry and free from lotion before
placing the electrode pads on your skin. Refer to the Pads User Guide.
Step 4 Press the ON/OFF button once to turn the power on
Step 5 Choose the output channel(s) to be used. You can use one channel at a time or both
simultaneously
Step 6 Select one of the seven mode
Step 7 Select the stimulation times
Step 8 Adjust the stimulation intensity
Step 9 Press the ON/OFF button once to turn the power off
DESCRIPTION OF OPERATION DIAGRAM
Step 1- Insert the 2 AAA batteries into the
device.
Make sure the unit is OFF. Slide the compartment
cover on the back of device downward until the
cover pops off. Insert 2 AAA batteries according to
the diagram inside the battery compartment. Close
the cover.

11
Step 2- Connect the electrode pads to the wires
and then connect the wires to the device.
Plug the connecting wires into the electrode pads.
Then connect the wires to the device’s output
channels. The A and B output channels can be
used simultaneously or one at a time. Select
channel by pressing CHA Button.
NOTE: If you connect wires to both A and B
outputs, you must turn on both A and B and have
pads connected. These pads MUST be placed on
the body for stimulation to occur.
Step 3- Put the electrode pads on the
stimulation –needed body area.
In order to achieve the best relief results. Place the
electrode pads around or on the top of your painful
areas. If possible, always use all the 4 electrode
pads at the same time. (If all 4 pads are being
used, both outputs must be turned on). Electrode
pads should be placed between 0.5″to 1.5″apart
from each other based on the relief area. Make
sure the pads stick rmly on the skin. Do not move
or remove the pads when the device is on.
Clean your skin before each use. Make sure your
skin is clean, dry and free from lotion before placing
the electrode pads on your skin.
Step 4- Press the ON/OFF button once to turn
the unit on
The LCD display will show 7 stimulation modes.
Step 5- Choose the output channel(s) to be
used for stimulation
Pressing the CHA button on the front of the unit
turn on and off the corresponding output channels.
(Both A&B are ON by default)
IMPORTANT: You must have wires inserted
into the output and pads placed on skin if the
output channel is turned on for stimulation to
occur. You can use one channel at a time or both
simultaneously as long as the output channel
is turned on, wires are connected and pads are
attached to skin.

12
Step 6- Select one of the seven stimulation
modes
Press the MODE button to toggle between
stimulation modes:
Mode1, Mode 2, Mode 3, Mode 4, Mode 5, Mode
6 and Mode7. LCD Screen indicates the current
mode.
Step 7- Select the stimulation times
Press the TIME button the stimulation The
stimulation time is 20 minutes each power on.
Timer range is 5 to 20 min.
Step 8- Adjust the stimulation intensity
Press the button will Decrease & Increase the
intensity of stimulation.
Note: With the increase of intensity, you may
experience sensations like tingling, vibration, pain,
etc. Therefore, gradually increase the intensity,
and stop increasing when a comfortable level is
reached.
Step 9- Press the ON/OFF button once to turn
the power off
After the device is turned off. Disconnect the wires
and electrode pads. Take the batteries out of the
unit if the device will not be in use for a long period
of time.
13 Accessories
The following accessories are included:
Connecting Wires
The lead wires consist of PVC material in the outside and thin copper wire on the inside. The
total length of the lead wire is 59.05 inches and there are 3 connectors on each wire. The one
connector on the left end is used to connect to the device and the 2 connectors on the other
end are used to connect to the electrode pads. The pulse generated by the device to the pads
through these connecting wires.
Electrode Pads (Up to 80 uses)
The electrode pads applied to MDTS100 is adopted the electrode pad manufactured by Wuxi
Jiajian Medical Instrument Co., Ltd and has been cleared by FDA in June 23, 2009 as K090198.

13
14 Electrode Pads User Guide
Clean skin thoroughly prior to each application of electrode pads. Pads will not stick well if any
lotion, make-up, or dirt is left on your skin.
Make sure the Electronic Pulse Stimulator is off before applying the electrodes to the skin.
1. Insert the pins of connecting wire into the wire connectors of each electrode pad (as
shown in image A)
2. Remove the electrode pads from the protective liner. Lift at the edge of the electrode pad
and peel from the liner. Do not pull on the lead wires when removing the electrode pads
from the protective liner or skin. The electrodes may become damaged (show in image B).
3. Apply rmly to the skin.
4. When not in use, return the pads to the protective liner (as show in image C). Store the
electrode pads in the re-sealable bag in a cool place, out of direct sunlight.
15 Quality Assurance Tests
The test result of each step should meet the following pass criteria. Otherwise, it is considered
failed.
KEY FUNCTION TEST
When the functional keys are pressed step by step, the outputs of the device should be identical
to the following description:
1. When the ON/OFF button at the off condition is pressed. The device is turned on, LCD
screen will show 7 modes. Minutes left, and A&B output channels.
2. When the MODE key is pressed, the corresponding mode is selected on the LCD screen.
3. Press the button to decrease or increase the stimulation intensity. The default level is
0.
4. The number in the top left corner display the remaining stimulation time.
LCD CHECK
The information displayed on the LCD screen should be identical to the following description:
Output Channels
Stimulation Timer
Level of Intensity
Battery indicator
current Stimulation Mode
16 Cleaning and Measurement
Use water or neutral detergent to clean the device rst, and then use a dry cloth to wipe it
again. The electrode pads included with the device are reusable up to 80 uses. They should

14
be replaced when their adhesiveness becomes weak. To insure proper use, The applied Self
Adhesive Replacement Gel Pads should be used. Do not let the sticky side of the electrode
pads touch anything, including your ngertips. Do not use damaged or broken wires.
Dispose of battery properly; following any applicable local battery disposal laws.
The use life of the device is ve years when it is used for 15 measurements every day and 20
minutes per one measurement.
Warning
• Water is prohibited in the host device, in order to avoid damaging the device or reducing
the safety and performance of the device.
• Please do not open the battery cover when the device is operated.
• Please do not clean and maintain the device when the device is operated.
• Please do not open the device enclosure, the device can only be maintained by personnel
authorized by the manufacturer.
• When the accessory of the device is damaged or failure, it must be the personnel
authorized by the manufacturers to replace the correct attachment.
• The host device should be cleaned at least once a month and can be cleaned by using
soft cloth dipped in small amount of water.
• The electrode pads can only be used by the single patient and the electrode pads is
required to be replaced periodically.
• Check the insulation of the output cable regularly, if there is any damage the cable should
be replaced immediately.
• When the battery is exhausted, the new battery should be replaced according to the
specication immediately.
17 Position for Use
Note:
1. The electrode pads should be applied rmly on the either side of the area where you feel the
pain.
2. Never apply electrodes on the throat or both sides of the neck,where the carotid sinus nerves
are located.
18 Troubleshooting
If your device is not operating properly, please check it for the following problems or conditions.
If the recommended action does not solve the problem, please return it to the Beijing Choice
Electronic Technology Co., Ltd for a replacement or repair of the device.
MALFUNCTION CAUSE SOLUTION

15
Stimulation is
weak or not
existent
Are the electrode pads in close
contact with the skin?
Remove, clean and place back on
the skin.
Are the electrode pads touching
each other? If so, separate the pads.
Are the wires connected to the
electrode pads and the main
device properly?
Disconnect, clean and reconnect
all the parts.
Are the batteries dead? Replace the batteries.
Skin turns red Did you stay with stimulation too
long?
Stop treatment or move to another
area.
Skin feels numb
Are electrode pads dirty? Clean with damp cloth or replace.
Do the electrode pads touch the
skin closely?
Remove and place again on the
skin.
Device does not
turn on
Are the batteries installed
correctly? Remove and install batteries.
Pads are not
sticky
Pads will deteriorate after multiple
uses.
Replace them with ChoiceMMed
Self-Adhesive Replacement Gel
Pads MDPS100
19 Symbols
Type BF applied part Attention, consult
accompanying document
Serial number Caution
Storage temperature and
humidity
“+”/“-” on the battery means
Positive/Negative Pole.
Please match the plus (+)
and minus signs in the
compartment
Date of manufacture Manufacturer information
Enclosure protection
degree Mode 1
Mode 2 Mode 3
Mode 4 Mode 5
Mode 6 Mode 7

16
Authorized representative in
the European community European union approval
No throwing into the trash
cans
20 Compliance Information for EMC Test
Electromagnetic emission
Emission test Compliance Electromagnetic Environment – guidance
Conducted and radiated
RF emissions
Group 11, Group 1,
Class B Home Healthcare environment
Electromagnetic immunity
Immunity test IEC 60601 test level Compliance Level Electromagnetic Environment –
guidance
Electrostatic discharge
(ESD) IEC 61000-4-2 ± 8kV contact
±15kV air ± 8kV contact
±15kV air
Special healthcare environment
The relative humidity should be
at least 50%.
Radiated RF
IEC 61000-4-3 10 V/m
80 MHz to 2.7 GHz 10 V/m
80 MHz to 2.7 GHz Home healthcare environment
Power
frequency (50/60Hz)
magnetic eld
IEC61000-4-8
30A/m 30A/m Home healthcare environment
Electromagnetic immunity to RF wireless communications equipment
Test frequency
(MHz) Banda) (MHz) Service a) Modulation b)
Maximum
power
(W)
Distance
(m)
Immunity test
level
(V/m)
385 380-390 TETRA 400
Pulse
modulation b)
18Hz
1.8 0.3 27
450 430-470 GMRS 460,
FRS 460
FMc)
±5kHz
deviation
1kHz sine
2 0.3 28
710
704-787 LTE Band 13,17
Pulse
modulationb)
217Hz
0.2 0.3 9745
780

17
810
800-960
GSM 800/900,
TETRA 800,
iDEN 820,
CDMA 850,
LTE Band 5
Pulse
modulation b)
18Hz
2 0.3 28
870
930
1720
1700-1990
GSM 1800;
CDMA 1900;
GSM 1900;
DECT;
LTE Band
1,3,4,25; UMTS
Pulse
modulation b)
217Hz
2 0.3 281845
1970
2450 2400-2570
Bluetooth,
WALN, 802.11
b/g/n, RFID
2450, LTE Band
7
Pulse
modulation b)
217Hz
2 0.3 28
5240
5100-5800 WLAN 802.11
a/n
Pulse
modulation b)
217Hz
2 0.3 95500
5785

18
INHALTSVERZEICHNIS
1 Lieferumfang...................................................................................................................................................19
2 Vorstellung......................................................................................................................................................19
3 Bestimmungsgemäße Verwendung................................................................................................................19
4 Verwendungszweck........................................................................................................................................19
5 Gegenanzeige ................................................................................................................................................19
6 Eigenschaften des MDTS100.........................................................................................................................19
7 Sicherheitswarnungen....................................................................................................................................20
8 Spezikationen ...............................................................................................................................................22
9 Vorgang einschließlich der folgenden Parameter:..........................................................................................23
10 So funktioniert das Gerät .............................................................................................................................28
11 Ihr Gerät verstehen.......................................................................................................................................28
12 Betriebsanweisungen ..................................................................................................................................28
13 Zubehör ........................................................................................................................................................31
14 Bedienungsanweisungen für die Elektrodenpads ........................................................................................32
15 Qualitätskontrolle..........................................................................................................................................32
16 Reinigung und Abmessung...........................................................................................................................33
17 Position für die Verwendung ........................................................................................................................33
18 Problembehebung ........................................................................................................................................33
19 Symbole........................................................................................................................................................34
20 Konformitätsinformationen für den EMV-Test...............................................................................................34
Other manuals for MDTS100
1
Table of contents
Languages: