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The MS6000 Bed Scale user manual provides essential safety instructions, installation guidelines, and operational procedures for the device intended to measure the weight of individuals with limited mobility. It emphasizes the importance of reading the manual thoroughly, adhering to safety precautions, and ensuring proper setup to achieve accurate measurements. The document also includes information on electromagnetic compatibility, maintenance, warranty, and disposal of the device.

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0% found this document useful (0 votes)
6 views

ms6000-en

The MS6000 Bed Scale user manual provides essential safety instructions, installation guidelines, and operational procedures for the device intended to measure the weight of individuals with limited mobility. It emphasizes the importance of reading the manual thoroughly, adhering to safety precautions, and ensuring proper setup to achieve accurate measurements. The document also includes information on electromagnetic compatibility, maintenance, warranty, and disposal of the device.

Uploaded by

elbjorne.mb
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
You are on page 1/ 40

USER MANUAL

MS6000
Bed Scale

Please keep the instruction manual at hand all the time for future reference.

1
Explanation of Graphic Symbols on Label/Packaging

Caution, consult Separate collection for


accompanying documents waste of electrical and
before use electronic equipment,
in accordance with
Directive 2002/96/EC

Manufacturer of medical Manufacturing year of


device medical device

Carefully read user manual Medical electrical


before installation and equipment with Type B
usage, and follow applied part
instructions for use.

Device catalogue number Authorized


representative in the
European Community

Manufacturer's batch or lot Device is a medical


number device

Serial number Unique Device Identifier

Device conforms to 93/42/EEC as amended


by 2007/47/EC Medical Device Directive. Four
digit number refers to Notified Body.

Device complies with International


Organization of Legal Metrology (Class III)
requirements (verified models only)

Device complies with EC directives (verified


models only)

M: Conformity label in compliance with


Directive 2014/31/EU for non-automatic
weighing instruments

16: Year in which conformity verification was


performed and the CE label was applied. (ex:
16=2016)

0122: Refers to Notified Body for metrology

2
Copyright Notice
Charder Electronic Co., Ltd.
No.103, Guozhong Rd., Dali Dist., Taichung City 41262 Taiwan
Tel: +886-4-2406 3766
Fax: +886-4-2406 5612
Website: www.chardermedical.com E-mail: info_cec@charder.com.tw

Copyright© Charder Electronic Co., Ltd. All rights reserved.


This user manual is protected by international copyright law. All content
is licensed, and usage is subject to written authorization from Charder
Electronic Co., Ltd. (hereinafter Charder) Charder is not liable for any
damage caused by a failure to adhere to requirements stated in this
manual. Charder reserves the right to correct misprints in the manual
without prior notice, and modify the exterior of the device for quality
purposes without customer consent.

Charder Electronic Co., Ltd.


No. 103, Guozhong Rd., Dali Dist.,
Taichung City, 41262 Taiwan

3
CONTENTS
I. Safety Notes .......................................................................... 5
A. General Information ............................................................ 5
B. EMC Guidance and Manufacturer's Declaration ........................ 8
II. Installation ..........................................................................12
A. Setting up weight bridges ...................................................12
B. Inserting Batteries .............................................................14
D. Using Adapter ...................................................................17
III. Indicator ............................................................................18
A. Indicator and Key Functions ................................................18
B. Display layout....................................................................19
IV. Using Device .......................................................................20
A. Performing measurement ....................................................20
B. Hold .................................................................................21
C. BMI ..................................................................................22
V. Advanced Operation .............................................................23
A. Pre-Tare ............................................................................23
B. Weight Tracking & Alarm .....................................................25
VI. Device Setup .......................................................................28
A. Setting Time & Date ...........................................................28
B. Device Setup .....................................................................29
VII. Setup USB Connection to PC ..............................................31
VIII. Wireless Connection ........................................................34
IX. Troubleshooting ..................................................................35
X. Product Specifications ..........................................................37
XI. Declaration of Conformity ...................................................40

4
I. Safety Notes

A. General Information
Thank you for choosing this Charder Medical device. It is designed to be
easy and straightforward to operate, but if you encounter any problems
not addressed in this manual, please contact your local Charder service
partner.

Before beginning operation of the device, please read this user manual
carefully, and keep it in a safe place for reference. It contains important
instructions regarding installation, proper usage, and maintenance.

Intended Use
This device is intended to measure the weight of subjects with limited
mobility, for diagnosis of weight-related issues by professionals.

General Handling
 Device should be placed on stable, flat, solid, non-slippery surface.
 Usage on soft surfaces (ex: carpet) may result in inaccurate results.
 Ensure all parts are properly locked and tightened before operating
the device.
 Device is intended to measure one subject at a time.

Safety Instructions
 Batteries should be kept away from children. If swallowed, promptly
seek medical assistance.
 Expected service life: 5 years.
 Always comply with appropriate regulations when using electrical
components under increased safety requirements.
 Ensure voltage marked on power supply matches mains power
supply.
 The device is intended for indoor use only.
 Observe permissible ambient temperatures for use

Environmental
 All batteries contain toxic compounds; batteries should be disposed
of via designated competent organizations. Batteries should not be
incinerated.

Cleaning
 Device surface should be cleaned using alcohol-based wipes.

5
Corrosive cleansing liquids should not be used. Pressure-washers
should not be used.
 Do not use large amounts of water when cleaning the device, as it
may cause damage to the internal electronics.
 Always disconnect device from mains power before cleaning.

Maintenance
 Device does not require routine maintenance. However, regular
checking of accuracy is recommended; frequency to be determined
by level of use and state of device. If results are inaccurate, please
contact local distributor.

Warranty/Liability
 The period of warranty shall be eighteen (18) months, beginning on
the date of purchase. Please retain your receipt as proof of purchase.
 No responsibility shall be accepted for damage caused through any
of the following reasons: unsuitable or improper storage or use,
incorrect installation or commissioning by the owner or third parties,
natural wear and tear, changes or modifications, incorrect or
negligent handling, chemical, electrochemical, or electrical
interference.
 All maintenance, technical inspections, and repairs should be
conducted by an authorized Charder service partner, using original
Charder accessories and spare parts. Charder is not liable for any
damages arising from improper maintenance or usage.

Disposal
 This product is not to be treated as regular household waste, but
should be taken to a designated collection points for electronics.
Further information should be provided by local waste disposal
authorities.

Warning
 Only the original adapter should be used with the device. Using an
adapter other than the one provided by Charder may cause
malfunction.
 Do not touch the power supply with wet hands.
 Do not crimp the power cable, and avoid sharp edges.
 Do not overload extension cables connected to the device.
 Route cables carefully, to avoid tripping.
 Keep device away from liquids.
 Do not remove the plug by yanking on the cable.
6
 Use only a correctly wired (100-240VAC) outlet, and do not use a
multiple outlet extension cable.
 Do not under any circumstances dismantle or alter the device, as this
could result in electric shock or injury as well as adversely affect the
precision of measurements.
 Do not place the device in direct sunlight, or in close proximity to an
intense heat source. Excessively high temperatures may damage the
internal electronics.

Incident Reporting
Any serious incident that has occurred in relation to the device should be
reported to the manufacturer, EU representative (if device is used in EU
member state), and competent authority of user/subject's member state.

7
B. EMC Guidance and Manufacturer's Declaration

Guidance and manufacturer’s declaration-electromagnetic emissions


The MS6000 Bed Scale is intended for use in the electromagnetic environment specified
below. The customer or the user of the device should assure that it is used in such an
environment.

Electromagnetic
Emission test Compliance
environment-guidance
RF emissions CISPR 11 Group 1 The device uses RF energy only for
its internal function. Therefore, its
RF emissions are very low and are
not likely to cause any interference
in nearby electronic equipment.

Class B The device is suitable for use in all


RF emissions CISPR 11 establishments, including domestic
establishments and those directly
Class A connected to the public low-voltage
Harmonic emissions IEC power supply network that supplies
61000-3-2
buildings used for domestic
Voltage fluctuations /flicker Compliance purposes.
emissions IEC 61000-3-3

8
Guidance and manufacturer’s declaration-electromagnetic immunity
The MS6000 Bed Scale is intended for use in the electromagnetic environment specified
below. The customer or the user of the device should assure that it is used in such an
environment.

IEC 60601 Compliance Electromagnetic


Immunity test
test level level environment-guidance

Electrostatic ± 8 kV contact ± 8 kV contact Floors should be wood, concrete


discharge(ESD) ± 2 kV, ± 4 kV, ± 2 kV, ± 4 kV, or ceramic tile. If floors are
IEC 61000-4-2 ± 8 kV, ± 15 kV ± 8 kV, ± 15 kV covered with synthetic material,
air air
the relative humidity should be
at least 30%
Electrical fast ± 2kV for + 2kV for power Mains power quality should be
transient/burst power supply supply lines that of a typical commercial or
IEC 61000-4-4
lines + 1kV for hospital environment.
+ 1kV for input/output
input/output lines
lines
Surge IEC ± 1kV line(s) to + 1kV line(s) to Mains power quality should be
61000-4-5 line(s) line(s) that of a typical commercial or
± 2kV line(s) to + 2kV line(s) to hospital environment.
earth earth
Voltage Dips, 0% UT for 0,5 0% UT for 0,5 Mains power quality should be
short interruptions cycle cycle that of a typical commercial or
and voltage 0% UT for 1 0% UT for 1 hospital environment. If the
variations on cycle cycle user of the device requires
power supply continued operation during
input lines IEC 70% UT(30% 70% UT(30% power mains interruptions, it is
61000-4-11 dip in UT) for dip in UT) for 25 recommended that the device
25 cycles cycles be powered from an
uninterruptible power supply or
0% UT for 5 s 0% UT for 5 s a battery.

Power 30 A/m 30 A/m The device power frequency


frequency(50/60 magnetic fields should be at
Hz) magnetic field levels characteristic of a typical
IEC 61000-4-8 location in a typical commercial
or hospital environment.

NOTE UT is the a.c. mains voltage prior to application of the test level.

9
Guidance and manufacturer’s declaration-electromagnetic immunity

The MS6000 Bed Scale is intended for use in the electromagnetic environment specified
below. The customer or the user of the device should assure that is used in such an
environment.
IEC 60601 test Compliance Electromagnetic
Immunity test
level level environment-guidance
Conducted RF 3 Vrms 3 Vrms Portable and mobile RF
IEC 61000-4-6 150 KHz to 80 MHz 150 KHz to 80 communications equipment
MHz
Radiated RF IEC 6 V in ISM bands should be used no closer to any
61000-4-3 between 0,15 MHz 6 V in ISM part of the device including
and 80 MHz bands between cables, than the recommended
80 % AM at 1 kHz 0,15 MHz and separation distance calculated
80 MHz
from the equation applicable to
3 V/m 80 % AM at 1
80MHz to 2,7 GHz kHz the frequency of the
transmitter.
3 V/m
80MHz to 2,7
Recommended separation
GHz
distance:
d = 1,2 √P
d = 1,2 √P 80MHz to 800 MHz
d = 2,3 √P 800MHz to 2,5 GHz

Where P is the maximum output


power rating of the transmitter
in watts (W) according to the
transmitter manufacturer and d
is the recommended separation
distance in metres (m).

Field strengths from fixed RF


transmitters, as determined by
an electromagnetic site surveya,
should be less than the
compliance level in each
frequency rangeb.

Interference may occur in the


vicinity of equipment marked
with the following symbol:

10
NOTE1 At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE2 These guidelines may not apply in all situations. Electromagnetic propagation is
affected by absorption and reflection from structures, objects and people.
a Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless)
telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV
broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic
environment due to fixed RF transmitters, an electromagnetic site survey should be
considered. If the measured field strength in the location in which the device is used
exceeds the applicable RF compliance level above, the device should be observed to
verify normal operation. If abnormal performance is observed, additional measures may
be necessary, such as re-orienting or relocating the device.
b Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.

Recommended separation distance between portable and mobile RF


communications equipment and the MS6000 Bed Scale
The device is intended for use in an electromagnetic environment in which radiated RF
disturbances are controlled. The customer or the user of the device can help prevent
electromagnetic interference by maintaining a minimum distance between portable and
mobile RF communications equipment (transmitters) and the device as recommended
below, according to the maximum output power of the communications equipment.
Rated maximum Separation distance according to frequency of
output power of transmitter m
transmitter
150 kHz to 80 80 MHz to 800 800 MHz to 2,5
MHz MHz GHz
W
d =1,2√P d =1,2√P d =2,3√P

0,01 0,12 0,12 0,23

0,1 0,38 0,38 0,73

1 1,2 1,2 2,3

10 3,8 3,8 7,3

100 12 12 23
For transmitters rated at a maximum output power not listed above, the recommended
separation distance d in metres (m) can be estimated using the equation applicable to the
frequency of the transmitter, where p is the maximum output power rating of the
transmitter in watts (W) according to the transmitter manufacturer.

NOTE1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range
applies.
NOTE2 These guidelines may not apply in all situations. Electromagnetic propagation is
affected by absorption and reflection from structures, objects and people.

11
II. Installation
A. Setting up weight bridges

1. Place weight bridges under bed next to bed castors.

2. Device should be placed on non-slippery, flat,


hard, level surface. Make sure bubble level
indicator is centered to ensure result accuracy.

Bubble indicator: Level

Not level

3. Connect weight bridges. All pins should be connected slowly and


carefully to avoid damage.

Blue cable should be plugged into blue port; yellow cable should be
plugged into yellow port.

12
Note: connect both weight bridges to one another using weight bridge
connecting wire. Connect indicator to weight bridge 2 (blue port).

4. Turn on device.

5. After device is turned on, push bed onto weight bridges. Two people
may be needed to complete procedure.

13
Note: take care not to catch connecting cable under platform or bed.
B. Inserting Batteries

1. Open battery housing cover

2. Accessing batteries

Take out the battery


housing

3. Use either rechargeable battery pack, or AA batteries

14
4. Ensure batteries are installed into the housing correctly

Rechargeable
Battery Housing

AA-size Battery Housing

5. Install the battery housing into the compartment, and make sure the
right side of housing pin is facing towards inside of the connecting
position

15
6. Slide back the cover to close the battery housing compartment. Turn
on power to confirm that battery is correctly installed.

Using Rechargeable Battery (optional)

The rechargeable battery should be recharged at least once every 3


months, regardless of if the device has been used. Battery can be
charged by plugging device's exclusive adapter into AC Connector Port.

After a long period in storage (e.g. >3 months), the battery should run a
full cycle (charge/discharge) to allow it to restore full capacity.

Ensure rechargeable battery housing is installed and inserted properly


into the compartment.

AC Connector Port

If prompt displays on the LCD, please charge battery


promptly to avoid battery damage.

16
D. Using Adapter
1. Connect adapter to indicator before connecting to mains power supply
2. Disconnect adapter from mains power supply before unplugging
adapter pin from indicator.

AC Connector Port

17
III. Indicator
A. Indicator and Key Functions

Key Functions

1. ON/OFF: Power on or power off

2. ZERO: Reset display to 0.0 kg display. Press and hold for 3


seconds to enter device settings.

3. M1-10: Save pre-tare values (up to 10)

4. PRE-TARE: Pre-tare the known weight of an object (ex: bed)


before beginning measurement. Press and hold for 3 seconds to call
up pre-tare values

5. PRINT: When printer or PC is connected to the scale, press this


key to print results

6. MONITOR WEIGHT: Track change in patient weight. Press and


hold for 3 seconds to enter weight monitor settings.

7. ALARM: Turn weight change alarm on/off, adjust volume of


alarm. Press and hold for 3 seconds to enter time settings

8. HOLD/BMI: Activate hold. Press and hold for 3 seconds to


enter BMI mode

18
9. CLEAR: Clear incorrect data input

10. ENTER: Confirm input

11. - 0-9: For entering digits

B. Display layout

PRE-TARE HOLD NET WEIGHT


Stable
symbol

Zero
symbol
Wireless
Negative
weight

Power kg

Setting increase in
weight limit

Weight monitor Height


function active

Setting decrease in
weight limit BMI

Weight change
alarm active

Definitions
Stable symbol: Indicates that weight is stable.
Zero symbol: Weight is at zero
Negative weight: Weight under zero.
Power: Device power level.

Charge or Insufficient
100% 75% 50% 25%
replace battery power

19
IV. Using Device
A. Performing measurement
Install weight bridges under the bed and connect all wires.

Switch on the device using key. The device will automatically


perform self-calibration, displaying software version. Once "0.00 kg"
appears on indicator, device is ready for measurement.

Note: If "0.00 kg" does not display on indicator, press key to zero
the device.

User can either select pre-tare bed weight, or deduct weight of bed at
point of measurement.

Using pre-tare bed weight (used when subject is already in bed):

1. Recall previously stored Pre-Tare


value (bed weight) from device
memory by pressing and holding

key for 3 seconds. Indicator


will display pre-tare value M1 first.
The pre-tare value will flash.

2. Press numeral keys 0~9 to select

pre-tare value. Press key to


confirm selection.

(for instructions on how to set


Pre-Tare, please refer to Setting
and Recalling Pre-Tare.

Scale will deduct weight of bed, and


minus (-) sign will appear in front of
Pre-Tare value.

3. Push bed (with subject) onto


weight bridges. Conduct
measurement.

20
Deduct weight of bed at point of measurement:
1. Push bed (without subject) onto
weight bridges.

2. Press key after stable


symbol appears on indicator. Display
will indicate "0.00 kg".

3. Guide subject to lie down upon


bed. Conduct measurement.

4. To clear tare value, remove bed


from weight bridges, and press

key.

Note: If total weight exceeds scale capacity (includes tare), indicator will
display "Err" prompt due to overload.

If subject's weight has difficulty stabilizing, the Hold function can be


used.

B. Hold
The hold function determines average weight, designed to be used if
subject's weight will not stabilize (ex: an active child).

Note: if fluctuation is too severe, average weight determination will be


difficult and hold may not function correctly

1. After recalling pre-tare weight (bed weight) from memory, scale will
deduct bed weight and (-) will appear in front of weight.
2. Push bed onto weight bridges.

3. Press the key. "HOLD" will be displayed on the indicator.


4. After a few seconds, the average weight will be displayed on the
indicator.

5. To release the locked weight, press the key again to return to


the device to normal mode.

Note: Hold function can be activated before or after bed is pushed onto
weight bridges.
21
C. BMI
After weight has been measured, BMI can be calculated.

1. Without removing bed from weight

bridges, press and hold the


key for 3 seconds to enter BMI mode.

Display will show last recorded


height. Left-most digit will flash.

2. Enter height using numeral keys


(ex: 170 cm). Input will automatically
move to next digit.

Press key to re-input.

After inputting height, press


to confirm.

Device will display subject's BMI


automatically.

Category BMI (kg/m2) Risk of obesity-related disease


Under < 18.5 Low
Normal 18.5-24.9 Average
Over 24.9-29.9 Slightly Increased
Obese I 30.0-34.9 Increased
Obese II 35.0-39.9 High
Obese III > 40 Very High
(World Health Organization adult BMI standards)

22
V. Advanced Operation
A. Pre-Tare
The Pre-Tare function is used to subtract the known weight of a
substance prior to weighing. The device can store 10 sets of pre-tare
values. Pre-tare values can be stored using two different methods: "Load
Weight", or "Input Manually".

After pre-tare weights have been stored, they can be recalled by holding

the key for 3 seconds.

1. Load Weight
DESCRIPTION EXAMPLE

Press key after loading


weight on the platform; the
indicator will display blinking "m"
symbol.

Press numeral key 0 ~ 9 to assign


this number with the current
pre-tare weight.

Press key to store pre-tare


weight; the indicator will make a
beep sound.

23
2. Input Manually
DESCRIPTION EXAMPLE

Press and hold key for 3


seconds. Left-most digit will begin
blinking.

If no further action is taken within


6 seconds, indicator will return to
normal mode
While digit is blinking:

Enter pre-tare weight using 0~9


keys.

Ex: to pre-tare 5.0 kg of weight,


press 0-0-5-0.

Ex: to pre-tare 13.5 kg of weight,


press 0-1-3-5.

Press key to confirm the


pre-tare weight.

Indicator will display minus sign to


the left of pre-tare weight value.

To save this pre-tare weight


value in memory:

Press key; the blinking "m"


symbol will appear on the display.

24
Press numeral key 0 ~ 9 to assign
this number with the current
pre-tare weight.

Press key to store pre-tare


weight; the indicator will make a
beep sound.

NOTE: Pre-tare weight must be under max capacity, otherwise screen

will show 0.00 after key is pressed, and the operator will have to
re-input pre-tare settings.

B. Weight Tracking & Alarm


Prepare bed; place pillows, blankets, and any other objects affecting
weight onto bed. Turn on device before pushing bed onto weight bridges.

After bed has been pushed onto


weight bridges, display will show
total bed weight on upper LCD.

Press key to tare the weight


of the bed, the scale will return to
"0.0 kg" reading.

25
Guide subject to lie upon bed.
Display now shows net weight of
subject. (*)

Press and hold key; the


subject's weight will lock, and the
middle display will display "0.0".

Arrow will point to "+ weight".


Use numeral keys 0~9 to set the
increase in weight limit and press

key.

The lower display will begin blinking,


pointing to the (-) weight limit. (**).

Use numeral keys 0~9 to set the


decrease in weight limit. The minus
(-) sign will appear in front of the
weight decrease value.

After setting the weight decrease

value, press the key. (**).

Indicator will return to "0.0".

Press key to turn on the


alarm.

The blinking arrow pointing to

sign means the Alarm


volume is at maximum. To decrease

26
volume level, press key
again, and the blinking arrow will
stop blinking.

To turn off the alarm, press the

key until the arrow


disappears.

*NOTE - If the Weight Tracking Function is activated, the original


subject's weight will be saved in memory. This function can be activated
only after the bed has been pushed onto the weight bridges, and the
subject is lying down on the bed.

**NOTE - The weight change range starts from 500g/- 500g, and can be
increased/ decreased by increments of 100g.

27
VI. Device Setup
A. Setting Time & Date

Press and hold key for 3 seconds to enter Time Setting mode.

Example: Inputting 2008, Dec 25, 8:00am

Year Setting
Enter year using numeral keys 0-9.

Press key once completed to


proceed to month & day setting.
Month & Day Setting.
Enter month, followed by day using
numeral keys 0-9.

Ex: December 25th is "12.25".


Input 1-2-2-5.

Press key once completed to


proceed to time setting.
Time Setting
Enter time (24hr format) using
numeral keys 0-9.

Ex: 08:00am is input by pressing


0-8-0-0.

Press key once completed to


confirm time settings and proceed
to confirmation.
Device will display new time and
date settings, cycling between year,
month & day, and time.

YYYY→MM.DD→:HH:MM

Press key to return to


normal weighing mode.

28
B. Device Setup

When the device is switched on, press and hold the key for about 3
seconds, until the display shows the "SETUP”, followed by "A.OFF” (first
option in setting menu).

In device setup:

to toggle next menu option

to toggle previous menu option

to confirm selection

Auto Power-Off: Instruct device to shut off automatically after a certain


period of time.

Press to toggle between options (120 sec / 180 sec / 240 sec /

300 sec / off), and to confirm selection.

Buzzer/Beep:
When function is turned on, beeping noise will be made when: indicator is
turned on, keys are pressed, and weight is stable.

Press to toggle between on/off, and to confirm selection.

Hold Stop: When Hold Stop is "on", Hold will deactivate after subject
leaves measurement platform.

Press to toggle between on/off, and to confirm selection.


29
Bluetooth (optional): If device has Bluetooth module installed,
Bluetooth function can be turned on or off.

Press to toggle between on/off, and to confirm selection.

Wi-Fi (optional): If device has Wi-Fi module installed, Wi-Fi function


can be turned on or off.

Press to toggle between on/off, and to confirm selection.

Wi-Fi Setting (optional): If device has Wi-Fi module installed, this


option will appear.

Press to toggle between on/off, and to confirm selection.

30
VII. Setup USB Connection to PC

For successful connection, PC hardware connected to device must be


compatible with USB 2.0 or above. Operators should select a USB cable
length that is most suitable to the operating environment.

1. Charder Smart Data Manager can be used to connect the device to a PC.
The software program can be downloaded from the Charder website:

[LINK URL] https://www.chardermedical.com/download.htm

2. Connect USB cable to device indicator and PC. Follow installation


instructions.

Program Setup
1. After installation of Charder Smart Data Manager is complete, software
will automatically search for COM port. Press [Connect]. Once connected,
[Connect] button will change to [Disconnect].

31
Conducting Measurement
1. Input subject's first name, last name, patient ID, date of birth
(DD/MM/YYYY), gender, and height (for BMI calculation) into software if
needed. Press [Clear] to clear all input.

NOTE: information can also be input after weight measurement.

2. Conduct measurement. If [Auto] is selected, results will be


transmitted from device to software automatically and displayed on the
left of screen. If [Manual] is selected, user must press "Collect".

32
Saving & Printing Results
1. Press [Save as] to save measurement results as .csv file on PC.
Default file name is same as user ID. (ex: 20190201.csv) To track
changes and multiple measurements for the same subject, we
recommend not changing the default file name.

2. Result example:

If previous results were saved in "20190201.csv", new results also need


to be saved as "20190201.csv" (overwriting old file) in order to save
multiple results for the same subject.

Results will be saved in chronological order of measurement.

33
3. Press the printer icon to print out result using a printer connected to
the PC.

VIII. Wireless Connection


If the device has the wireless or bluetooth module installed, the indicator
can transmit measurement results wirelessly. Please see Charder
wireless or bluetooth software instructions for details.

34
IX. Troubleshooting
Before contacting your local Charder distributor for repair service, we
recommend considering the following troubleshooting procedures:

Self-inspection

1. Device will not power on


 If battery power is depleted, replace with new batteries
 If batteries are not used, check if the power adapter is plugged into
the device properly. Check if power adapter is plugged into mains
properly

2. Indicator showing "0000" ZERO SPAN out of range


 Interference due to factors such as RF disturbance or ground
vibration. Relocate device to location without interference and try
again
 Unstable platform feet - adjust level according to bubble level
indicator and try again
 External objects interfering with measurement platform. Clear
platform of objects and try again
 Device may not function properly on soft surfaces such as carpets or
lawns. Relocate device to location with solid, stable floor
 If the steps above cannot resolve the problem, re-calibration may be
required to correct weighing accuracy

3. Connection failure for data transmission to PC or printer


 Ensure cables are connected correctly between indicator and PC or
printer
 Ensure printer is supplied with power. Ensure PC software is set up
properly as indicated in this manual

Distributor support required

If the following errors occur, we recommend contacting your local


Charder distributor for repair or replacement services:

1. Device will not power on


 Faulty on/off key
 Broken or damaged wires causing short circuit or faulty connection
 Safety fuse burnout
 Faulty Adapter

35
2. Indicator damage
 Possible hardware defects include: uneven brightness in LCD screen,
blurred text, smeared rainbow screen, incorrect decimal display
 Unable to save or read data
 Indicator shows "ERRL" after device is switched on
 Keys not responding
 Buzzer malfunction

Error Messages
Error Message Reason Action
Low battery warning Replace batteries, or
Voltage of battery is too plug in AC adapter
low to operate device

Overload Reduce weight on


Total load exceeds measurement
device's maximum platform and try again
capacity
Counting Error (too Error normally caused
high) by faulty loadcell or
Signal from loadcells too wiring. Please contact
high distributor
Counting Error (too Error normally caused
low) by faulty loadcell or
Signal from loadcells too wiring. Please contact
low distributor
Zero count over Re-calibration
calibration zero range required. Please
+10% while power on contact distributor
Zero count under Re-calibration
calibration zero range required. Please
-10% while power on contact distributor

Program Error Error normally caused


Fault with device software by faulty loadcell or
wiring. Please contact
distributor

36
X. Product Specifications
Model MS6000
Display DP3710
300 kg x 0.1 kg,
Capacity
300-600 kg x 0.2 kg
Weight Accuracy ± 1.5e
Measurement
OIML Class III

LCD Screen 1.0-inch LCD screen (5 1/2 digits)

Overall 1256(W) x 230(D) x 61(H) mm


Dimensions
Weighing
1000(W) x 160(D)
Area
Device Weight 11.4 kg (each weighing bridge)
On/Off, Zero, Hold/BMI, Print,
Key Functions Pre-Tare, Clear, Enter, M1-10, Monitor
Weight, Alarm, 0~9
USB, Wireless Module (optional)
Data Transmission NOTE: Device should be connected to
network by qualified distributors only
Rechargeable battery pack (optional)
Power Supply or 6 AA batteries /
Power adapter
Operation Temperature &
0℃~40℃ 15% / 85% RH
Humidity
User manual*1, Weighing bridge*2,
Connecting cable*1, USB transfer
Standard Accessories
cable*1, Bracket set for wall
mount*1, Power adapter*1
Optional Accessories Thermal Printer

37
Warning
The device is only compatible with the power adapters specified below.

AMP DRAWING NO. CE APPROVED TYPE TYP Adapter


VOLTAG NO. / MODEL NO. E plug
E
12V 2A AD-8058(AD-0521) UE24WU-120200SPA US
AD-8057(AD-0520) UE24WV-120200SPA EU
AD-8056(AD-0519) UE24WB-120200SPA UK
AD-8074(AD-0534) UE24W4-120200SPAS AU

38
Notes

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39
XI. Declaration of Conformity
This product has been manufactured in accordance with the harmonized
European standards, following the provisions of the below stated
directives:

93/42/EEC as amended by 2007/47/EC


Medical Device Directive

2014/31/EU
Non-automatic Weighing Instruments
Directive

Please see separate document showing on sticker of device for above CE


marking.

Authorized EU Representative:

Manufactured by:
Charder Electronic Co., Ltd.
No.103, Guozhong Rd., Dali Dist.,
Taichung City, 41262 Taiwan (R.O.C.)

CD-IN-00014 REV 007 04/2021

40

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