CONTENTS I. Explanation of Graphic Symbols on Label/Packaging..... 4 II. Copyright Notice ..............6 III. Safety Notes ............... 7 A. General Information ............7 B. EMC Guidance and Manufacturer's Declaration .......11 IV. Installation .................15 A. Unfolding device ..............15 B. Using adapter and charging battery ........18 C.
I. Explanation of Graphic Symbols on Label/Packaging Meaning Text/Symbol Caution, consult accompanying documents before use Separate collection for waste of electrical and electronic equipment, in accordance with Directive 2002/96/EC. Do not dispose of device with everyday waste Name and address of device manufacturer, and year/country of manufacture Carefully read user manual before installation and usage, and follow instructions for use.
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Device complies with EC directives (verified models only) M: Conformity label in compliance with Directive 2014/31/EU for non-automatic weighing instruments 20: Year in which conformity verification was performed and the CE label was applied. (ex: 16=2016) 0122: Identifier for metrology Notified Body Device is a Class III scale in compliance with Directive 2014/31/EU (verified models only) Name and address of entity importing device (if applicable)
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.
III. 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.
(c) Language - Able to read the language of instruction manual and on-screen instructions (d) Qualifications - No special certifications or qualifications required Residual risk evaluation (a) All foreseeable risks have been evaluated and considered acceptable. Generally speaking, the most likely risk caused by incorrect usage of the device is less accurate measurement (or inability to use device to acquire measurement), which does not pose imminent physical risk to patient or user.
Charder service partner, using original Charder accessories and spare parts. Charder is not liable for any damages arising from improper maintenance or usage. Dismantlement of the device will void the warranty.
Warning ◼ The collapsible frame should be handled with caution. Keep fingers, hands, or other parts of the body clear when folding or unfolding frame, to avoid injury. Incident Reporting Any serious incident that has occurred in relation to the device ◼...
B. EMC Guidance and Manufacturer's Declaration Guidance and manufacturer’s declaration-electromagnetic emissions The product is intended for use in the electromagnetic environment specified below. The customer or the user of the product should assure that it is used in such an environment. Electromagnetic Emission test Compliance...
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Guidance and manufacturer’s declaration-electromagnetic immunity The product is intended for use in the electromagnetic environment specified below. The customer or the user of the product should assure that it is used in such an environment. Immunity IEC 60601 Electromagnetic Compliance level test test level environment-guidance...
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Guidance and manufacturer’s declaration-electromagnetic immunity The product is intended for use in the electromagnetic environment specified below. The customer or the user of the product should assure that is used in such and environment. IEC 60601 Compliance Electromagnetic Immunity test test level level environment-guidance...
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The product is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the product can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the product as recommended below, according to the maximum output power of the communications equipment.
IV. Installation A. Unfolding device Device should arrive in folded form. Rotate footrests into position. Raise seat back until joint locks Pull frame lock to Lift handles until raise seat back they automatically lock in place...
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To lower handles, press locks down Raise armrests into position...
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Engaging wheel brakes Wheel brakes must be engaged prior to measurement. Press down on brakes to engage. Brakes engaged...
B. Using adapter and charging battery 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.
2. Accessing batteries 3. Place new battery pack into housing, and insert into indicator 4. Close battery housing compartment cover. Turn on power to confirm that battery is correctly installed. D. Optional Accessories This device is compatible with a variety of accessories. Please consult their respective user manuals for assembly instructions: a.
V. Indicator A. Indicator and Key Functions Key Function POWER Power on or power off. Reset display to 0.0 kg display. Press and TARE/ZERO hold for 6 seconds to enter device settings. Determine stable weighing value - used HOLD when weight is unstable. Save pre-tare values (up to 10 sets can be MEMORY stored in device memory).
B. Display layout Quantity of Patient ID data Information PRE-TARE awaiting Nurse ID Wi-Fi transfer Battery status Transfer HOLD Scanner Stable Weight Zero Unit Height Capacity Graduation Definitions Quantity of data awaiting transfer: If device is not connected wirelessly, measurement results will be temporarily stored in device. Once device is connected, operator can press Transfer to send results wirelessly.
VI. Basic Operation 1. Switch on the device using key. The device will automatically perform self-calibration 2. Once "0.0" appears on indicator, device is ready for use NOTE: If "0.0" does not display on indicator, press [TARE/ZERO] key to zero the device. A.
device model. 3. After the phone/tablet/PC is connected to the device, the wireless symbol will change from 4. Device is now ready to send results wirelessly to phone/tablet/PC. 5. Before or after measurement, press the [HOLD] key. "HOLD" will be displayed on the indicator.
2. Enter height using numeral keys (ex: to input 170 cm, press 1-7-0-0). Press [CLEAR] key to re-input. 3. After inputting height, press [Enter] to confirm. 4. Proceed to weigh subject as usual. Indicator will display weight, height, and BMI. 5.
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Input Pre-Tare Value DESCRIPTION EXAMPLE Press [PRE-TARE] key. Input pre-tare weight value, starting from the left 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 [Enter] key to confirm the pre-tare weight.
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Save a Pre-Tare value DESCRIPTION EXAMPLE Press and hold [MEMORY] key for 3 seconds. Input the number for this pre-tare setting (between 01-10). Ex: To save memory set 3, press 0-3. Press the weight value box on the screen (marked in the red box to the right) Enter pre-tare weight using 0~9 keys.
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Recall Pre-Tare Value DESCRIPTION EXAMPLE Press [MEMORY] key to toggle between Pre-Tare settings saved in device (between 01-10). NOTE: to add new Pre-Tare value, please press and hold [MEMORY] key for 3 seconds to enter settings (see "Save a Pre-Tare value" above)
VII. Device Setup Press and hold [TARE/ZERO] key for 6 seconds to enter General Setting mode. Press menu options on the touchscreen to adjust settings. Auto Off Time: Instruct device to shut off automatically after a certain period of time. Auto off options: 120 sec / 180 sec / 240 sec / 300 sec / off Backlight: adjust backlight brightness.
Data Transfer: If enabled, all data fields (patient ID, weight, height) need to be completed to transfer data. If fields are incomplete (ex: only weight, no height or ID), data will not be transferred. Options: Enable / Disable Date/Time: Set device time. (Format: YYYY/MM/DD HH:M) WiFi Settings: Send results via direct transfer or via network (set Access Point if selected) G-Compensation: Authorized distributor can adjust gravity...
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 ◼...
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Error Messages Error Message Action Please charge battery using adapter, or replace battery Maximum weight exceeded. Reduce weight on platform before attempting measurement If problem persists, please contact distributor Re-calibration may be required. If problem persists, please contact distributor Re-calibration may be required. If problem persists, please contact distributor If problem persists, please contact...
X. Product Specifications A. Device Information Model MS5480 Display DP4800 250kgx 0.1kg Capacity 550 lb x 0.2 lb Accuracy ± 1.5e Weight Measurement Unit kg / lb LCD Screen Color LCD touchscreen Overall 590(W) x 1020(D) x 960(H) mm Height: 470mm...
B. Power Adapter Standards Warning Only the original adapter should be used with the device. Using an adapter other than the one provided by Charder may cause malfunction. Amp Voltage: 5V/2A Drawing No: CD-AD-00023 DRAWING CE APPROVED TYPE NO. /...
XI. Declaration of Conformity This product has been manufactured in accordance with the harmonized European standards, following the provisions of the below stated directives: (EU) 2017/745 Regulation on Medical Devices 2014/31/EU Non-automatic Weighing Instruments Directive (OIML models only) RoHS Directive 2011/65/EU and Delegated Directive (EU) 2015/863 Radio Equipment Directive 2014/53/EU (applicable if wireless module is used)
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