Mindray BeneFusion SP3 Vet Operator's Manual
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Mindray BeneFusion SP3 Vet Operator's Manual

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BeneFusion SP3 Vet
Syringe Pump
Operator's Manual

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Summary of Contents for Mindray BeneFusion SP3 Vet

  • Page 1 BeneFusion SP3 Vet Syringe Pump Operator’s Manual...
  • Page 3 © Copyright 2018-2019 Shenzhen Mindray Scientific Co., Ltd. All rights reserved. Release date: March 2019 Revision: 4.0...
  • Page 4 Scientific) owns the intellectual property rights to this product and this manual. This manual may refer to information protected by copyrights or patents and does not convey any license under the patent rights of Mindray Scientific, nor the rights of others.
  • Page 5 Mindray Scientific or repairs by people other than Mindray Scientific authorized personnel.
  • Page 6 Preface Manual Purpose This manual contains the instructions necessary to operate the product safely and in accordance with its function and intended use. Observance of this manual is a prerequisite for proper product performance and correct operation and ensures animal and operator safety. This manual is based on the maximum configuration and therefore some contents may not apply to your product.

  • Page 7: Table Of Contents

    Contents 1 Safety ........................1-1 1.1 Safety Information ....................1-1 1.1.1 Warnings ....................1-2 1.1.2 Cautions ....................1-3 1.1.3 Notes .......................1-4 1.2 Equipment Symbols ....................1-4 2 Overview ........................2-1 2.1 Description ......................2-1 2.1.1 Intended Use ...................2-1 2.1.2 Contraindications ..................2-1 2.1.3 Appearance, Parts and Features ............2-1 2.2 Host ........................2-2 2.2.1 Front View ....................2-2 2.2.2 Rear View ....................2-4...
  • Page 8 4.2.3 Change the Syringe.................4-3 4.2.4 Select Syringe Brands ................4-4 4.2.5 Parameter Memory Function..............4-4 4.2.6 Select Infusion Mode ................4-4 4.2.7 Purge Air ....................4-5 4.2.8 Set Infusion Parameters ................4-5 4.2.9 Infusion ....................4-5 4.2.10 Infusion Pause ..................4-6 4.2.11 BOLUS ....................4-6 4.2.12 Change the Rate during Operation ............4-6 4.2.13 Complete ....................4-7 4.2.14 Standby ....................4-7 4.2.15 Turn off the Pump ..................4-7...
  • Page 9 8.3 Alarm Handling Rules ..................8-2 8.4 Alarm Countermeasures ..................8-3 9 Battery ........................9-1 9.1 Battery Performance Optimization ..............9-2 9.2 Check the Battery ....................9-2 9.3 Battery Recycling....................9-3 10 Preservation and Sanitation ................10-1 10.1 Description ...................... 10-1 10.2 Cleaning ......................10-1 10.3 Disinfection ..................... 10-2 11 Maintenance ......................
  • Page 10 D Symbols and Terms .................... D-1 D.1 List of Units ......................D-1 D.2 List of Symbols ....................D-2 D.3 List of Terms ....................... D-2 D.4 List of Unit Conversion ..................D-3 E Toxic and Hazardous Substances or Elements ..........E-1 F Declaration of Conformity ..................

  • Page 11: Safety

    Safety 1.1 Safety Information WARNING  Indicates a potential hazard or unsafe practice that, if not avoided, could result in death, serious injury or damage to product/property. CAUTION  Indicates a potential hazard or unsafe practice that, if not avoided, could result in minor personal injury, product malfunction or damage to product/property.

  • Page 12: Warnings

    1.1.1 Warnings WARNING  Device, cables and accessories must be inspected before use to guarantee their normal and safe operation.  This equipment can only be connected to the socket with ground protection. Please adopt a rechargeable battery instead of the socket as the power supply if the socket is not provided with a ground lead.

  • Page 13: Cautions

    which is a non-standard consumable or a consumable without calibration, please contact the company for calibration service.  Do not touch the animal when connecting the peripheral equipment via the input/output signal ports to prevent animal leakage current from exceeding the requirements specified by the standard. ...

  • Page 14: Notes

    1.1.3 Notes NOTE  Install the equipment in a position where it can be easily accessed for inspection, operation and maintenance. Keep this Operator’s Manual near to the equipment for future ease of  reference.  The software was developed in compliance with IEC62304. The possibility of hazards arising from software errors is minimized.
  • Page 15 Stop Menu Move up/Increase Move down/Decrease Move left Move right Configured wireless Non-ionizing module and connected electromagnetic radiation successfully DEFIBRILLATION-PROOF Night mode TYPE CF APPLIED PART Date of manufacture Manufacturer THIS WAY UP Keep dry Fragile, handle with STACKING LIMIT BY care NUMBER Protected against solid...

  • Page 16: Overview

    Overview 2.1 Description 2.1.1 Intended Use The syringe pump is used in conjunction with the syringe to control the dose of liquid infused into the animal’s body. The syringe pump is expected to be used in institutes or units with healthcare capabilities.

  • Page 17: Host

    2.2 Host 2.2.1 Front View 1. Alarm light The alarm light indicates different alarm levels in different colors and flash frequencies, please refer to Chapter 8 Alarms for details. 2. Display Used for displaying infusion parameters and relevant content. 3. <DIRECTION> Used for adjusting value, change lines and pages.
  • Page 18 9. <AUDIO PAUSED> Pauses alarm sound. 10. <POWER> Used for turning power on, entering in standby state and turning off operations. 11. <MENU>  Used for entering [Main Menu] interface.  Under operation status, press and hold this key to lock; in locked state, press and hold this key to unlock.

  • Page 19: Rear View

    2.2.2 Rear View 1. Product label 2. Pole clamp mounting holes (two) 3. AC power supply port Connection for the AC power cord. 4. Multifunction interface with the following functions:  DC power supply port  RS232 interface  Nurse call interface 2.2.3 Side View 1.

  • Page 20: Bottom View

    1. Clip 2. Syringe fixation clamp 3. Slot 4. Spindle clamp 5. Slider 6. Handle 2.2.4 Bottom View 1. Speaker hole...

  • Page 21: Screen Display

    2.3 Screen Display This syringe pump has a monochrome LCD screen. The display information comprises three main parts: 1. Title bar Displays current infusion mode, drug information, alarm information, battery icon, and etc. 2. Parameter area Displays every parameter and the parameter value of the current screen. 3.

  • Page 22: Installation And Setting

    Installation and Setting 3.1 Installation WARNING  Equipment assembly and refit (including correct protective grounding connection) during life period must be carried out by maintenance technicians whom are trained and licensed by the manufacturer, and evaluated according to the specified IEC60601-1. Please contact the company if you have any queries.

  • Page 23: Out Of Box Audit (Ooba)

    3.1.1 Out of Box Audit (OOBA) Please check the packing case carefully before opening the box. If there is any damage, please contact the distributor or manufacturer immediately. WARNING  The packaging materials must be kept out of the reach of children. They must be disposed of in compliance with local laws and regulations or the hospital policy on waste management.

  • Page 24: Mount The Clamp

    3.1.3 Mount the Clamp 3.1.3.1 Standard Pole Clamp 1. Align the mounting holes on the pole clamp with the mounting holes on the back side of the machine, and tighten the screws. 2. Turn counterclockwise to loosen the pole clamp until an IV stand can be inserted in.

  • Page 25: Fix Benefusion Ds3 Infusion Supervision System (Optional)

    3.1.4 Fix BeneFusion DS3 Infusion Supervision System (Optional) The device can be located in the BeneFusion DS3 Infusion Supervision System. NOTE  All components of the system are suitable for use in animal environment.  Removing power cord is to disconnect equipment from power supply. Please ensure suitable clearance around the System to facilitate connect and remove power cord.

  • Page 26: Conventional Settings

    WARNING  The earthing wire in the three-plug connector should be grounded, if there is a doubt whether the AC power system is grounded or not, please adopt the built-in battery and contact an electrical technician at the hospital or the company. ...

  • Page 27: Set Language

    3.2.3 Set Language Select [Main Menu]→[User Maintenance]→Input User Maintenance Password→[Language]. Select from the [Language] according to actual needs. 3.2.4 Set Date and Time Select [Main Menu]→[User Maintenance]→Input User Maintenance Password→[Date and Time]. Set [Time] and [Date]. Select [Time format]: [24h] or [12h]. Select [Date format]: [yyyy-mm-dd], [mm-dd-yyyy] or [dd-mm-yyyy].

  • Page 28: Basic Operation

    Basic Operation 4.1 Infusion Flow Chart Turn pump on Press to activate and turn on the pump, the pump will run start-up checks and display the start-up screen; Load syringe Please refer to 4.2.2 Load the Syringe; Select according to the syringe brand currently being Select syringe brand used;...

  • Page 29: Operational Procedures

    4.2 Operational Procedures 4.2.1 Turn on the Pump To turn on the device, follow this procedure: Perform a safety inspection referring to 11.1 Inspection before turning on the pump. Press , the system will initiate the self-test and the screen will display the [System Self-test] interface: ...

  • Page 30: Change The Syringe

    Load syringe according to the following method: 1. Open the syringe fixation clamp, squeeze the handle to open the clip, and then move the slider to the appropriate position. 2. Align the syringe flange with the slot, then load it into the slot, and clamp the syringe.

  • Page 31: Select Syringe Brands

    4.2.4 Select Syringe Brands On the [Syringe Selection] screen, press to select the syringe brand and size of the syringe currently being used, and press for confirmation. WARNING  A new syringe brand should be calibrated when used for the first time. CAUTION ...

  • Page 32: Purge Air

    4.2.7 Purge Air During infusion, the user should prevent air bubbles from entering the blood with the liquid drug, which may form an aeroembolism and put animals in serious danger. Therefore, air bubbles in the syringe and extension cannula should be eliminated before the infusion.

  • Page 33: Infusion Pause

    NOTE  When in running status, if there is no operation in other interface over 2 minutes, it will return to the running screen automatically. 4.2.10 Infusion Pause During infusion, if changing the drug liquid or syringe is needed, press to enter the [Pause] interface to stop the infusion.

  • Page 34: Complete

    4.2.13 Complete If [VTBI] is not set during the infusion, when the time in which the remaining liquid needs to reach [Time Near End], the [Syringe Near Empty] alarm will be triggered, and this alarm can be cancelled automatically until the syringe is empty. Set [Time Near End], please refer to 6.6 Time Near End.

  • Page 35: Infusion Mode

    Infusion Mode 5.1 Rate Mode Mode Parameters Parameter Range 5ml syringe: 0.1-150ml/h 10ml syringe: 0.1-300ml/h Rate 20ml syringe: 0.1-600ml/h 30ml syringe: 0.1-900ml/h Rate Mode 50ml/60ml syringe: 0.1-2000ml/h VTBI 0.1-9999ml Time 00:00:01-99:59:59 h:m:s...

  • Page 36: Time Mode

    5.2 Time Mode Mode Parameters Parameter Range Time 00:00:01-99:59:59 h:m:s VTBI 0.1-9999ml 5ml syringe: 0.1-150ml/h Time Mode 10ml syringe: 0.1-300ml/h Rate 20ml syringe: 0.1-600ml/h 30ml syringe: 0.1-900ml/h 50ml/60ml syringe: 0.1-2000ml/h 5.3 Body Weight Mode 1. Select [Main Menu]→[User Maintenance]→Input User Maintenance Password→[BW Mode Configuration].
  • Page 37 Mode Parameters Parameter Range Weight 0.1-300.0 kg/0.2-660.8 lb Drug amt. 0.1-99999 Drug amt. unit ng, μg, mg, g, mU, U, kU, EU, mmol, mol, kcal, mEq Volume 0.1-9999ml Conc. 0.1-9999 ng/ml, μg/ml, mg/ml, g/ml, mU/ml, U/ml, kU/ml, Conc. unit EU/ml, mmol/ml, mol/ml, kcal/ml, mEq/ml Dose Rate 0.1-9999 Body...

  • Page 38: Intermittent Mode

    5.4 Intermittent Mode In Intermittent Mode, by setting the rate, Intmt. vol., Intmt. time and VTBI to control the infusion. It is suitable for the infusion of long-term analgesia drugs. Mode Parameters Parameter Range 5ml syringe: 0.1-150ml/h 10ml syringe: 0.1-300ml/h Rate 20ml syringe: 0.1-600ml/h 30ml syringe: 0.1-900ml/h...

  • Page 39: Setting Parameters

    Setting Parameters 6.1 KVO KVO (Keep Vein Open) means to keep the vein open, during which the syringe pump continues infusion at a very low rate after finishing the infusion in order to prevent blood backflow or vascular occlusion. Select [Main Menu]→[General Options]→[KVO Rate]. Select [KVO Rate]: 0.1-5.0ml/h is adjustable.

  • Page 40: Occlusion Pressure

    6.3 Occlusion Pressure Occlusion pressure is adjustable, which can meet the requirements for occlusion pressure of different animals during infusion. Pressure in the infusion tube can be measured by the built-in pressure sensor, pressure can be calculated by the internal CPU, which is compared with the preset occlusion alarm threshold.

  • Page 41: Automatic Pressure Release Function (Anti-Bolus)

    6.3.4 Automatic Pressure Release Function (Anti-Bolus) When occlusion occurs, infusion will stop and the [Occlusion] alarm will be triggered. After the alarm is triggered, the motor is reversed, and the cannula pressure is then released. This prevents an additional aggressive dose to the animal after the occlusion is eliminated.

  • Page 42: Commonly Used Syringes

    6.7 Commonly Used Syringes There are multiple built-in commonly used syringe brands in the syringe pump, making it convenient for the user to select from. Only 5ml, 10ml, 20ml, 30ml and 50ml/60ml syringes that comply with national standards should be used with this syringe pump.

  • Page 43: Other Functions

    Other Functions 7.1 History Record The syringe pump when in use will produce some key data stored in [History Record], providing foundation for the treatment review and maintenance review at a later period. The attribute of recording events includes action, time and description. A record is created once an event occurs.

  • Page 44: Wireless Networking (Optional)

     Alarm level: Three options: [High], [Medium] and [Low].The system sends nurse call signals according to the alarm at the selected alarm level or above. WARNING  Non-medical personnel are forbidden to modify the nurse call setting.  The nurse call function must be used in conjunction with a special cable. NOTE ...

  • Page 45: Data Export

    descriptions, please refer to the instructions of CIMS. Normal communication of the pump and CIMS depends on whether the network connection is successful, operators are unable to observe the operation status of the pump in real time when the communication is interrupted. After the network connection settings of the pump and CIMS are modified, operators shall reset the network connection as required in the manual to ensure the communication of the pump and CIMS are restored.

  • Page 46: Alarms

    Alarms The alarm is used in order to alert the medical staff by means of sound and light when abnormal situations occur during the infusion procedure which can lead to infusion changes or when the infusion of the animal cannot continue due to the unexpected breakdown or pause/delay of the syringe pump.

  • Page 47: Multi-Level Alarm Rules

    8.2.1 Multi-level Alarm Rules When several alarms occur simultaneously, the alarms proceed according to the following rules:  When several alarms at different levels occur, the visible alarms and audible alarms are consistent with the highest-level alarms.  When several alarms at different levels occur, only the highest-level alarm is displayed, and after it is cancelled, the lower-level alarm will then be displayed.

  • Page 48: Alarm Countermeasures

    8.4 Alarm Countermeasures WARNING  When an alarm is triggered, the animal's condition should be checked firstly and operation should only be allowed to proceed after the reason for the triggering of the alarm is ruled out. When an alarm is triggered, please follow these steps and take appropriate action: 1.

  • Page 49: Battery

    Battery WARNING  The battery can not be disassembled. The battery should be changed by maintenance staff designated by the company only. Changing the battery incorrectly or changing battery by personnel who has not received suitable training may cause such danger as overtemperature, fire or explode.

  • Page 50: Battery Performance Optimization

    The power supply by the battery can only be sustained for a limited period of time. The [No Battery] alarm will be triggered when the battery voltage is too low, and red alarm light will flash. The alarm will continue within the remaining time of the battery’s electric quantity and cannot be paused.

  • Page 51: Battery Recycling

    NOTE  The lifespan of the battery depends on how frequently it is used and on how long it has been used, battery capactiy decreases with increase in charging and discharging times. If the maintenance and storage of the battery is appropriate, the lifespan of the Lithium battery is no less than 300 times of full charging and discharging.

  • Page 52: Preservation And Sanitation

    Preservation and Sanitation The pump must be cleaned or disinfected using the materials and methods listed in this section. The manufacturer will not be responsible for any damage or accident caused by cleaning and disinfection using other materials and methods. The manufacturer shall not be held responsible for the efficacy of the following chemicals or methods for infection control.

  • Page 53: Disinfection

    To clean your equipment, follow these rules: Turn off the pump and disconnect the AC power source line. Wipe the display screen after soft cotton balls absorb an appropriate amount of detergent. Use a piece of soft cloth which absorbs a modest amount of cleaning agent to wipe the surface of the device.

  • Page 54: Maintenance

    Maintenance WARNING  To avoid electric shock, stop using the device if you find its housing has signs of broken. Contact the service personnel for help in that case.  The hospital or medical facility using this syringe pump must set up a comprehensive maintenance plan.

  • Page 55: Maintenance Plan

    11.2 Maintenance Plan The following tasks must be conducted by professional maintenance personnel approved by the company. Please contact the company if the following maintenances are needed. Must clean and disinfect the device before the test or maintenance. Inspection/Maintenance Items Frequency Once every two years.

  • Page 56: Safe Disposal And Recycling

    Press and the syringe pump starts automatic calibration. The screen prompts [Calibration successful] after the calibration is successful. Press to exit the current interface. Please align the front end of the plunger rod's sealing plug with the full scale position mark NOTE ...

  • Page 57: Accessories

    Accessories WARNING  Use the accessories specified in this chapter only. Other accessories may cause damage to this syringe pump, or cannot reach the specification in this manual.  Please do not replace an accessory if its package or itself is damaged. Materials 009-002755-00 009-002756-00...

  • Page 58: A Product Specifications

    Product Specifications A.1 Safety Specifications A.1.1 Product Classification Classifications of this syringe pump according to the IEC60601-1 standard are as follows: Safety Components Host Type of protection Class I against electrical shock Degree of protection Type CF defibrillation proof against electrical shock Ingress Protection IP34 Degree of safety of...

  • Page 59: Operating Environment

    A.1.2 Operating Environment Work environment Temperature 5-40º C Humidity 15-95%, non-condensing Atmospheric pressure 57-106 kPa Storage environment Temperature -20-60 º C Humidity 10-95%, non-condensing Atmospheric pressure 50-106 kPa Storage conditions Corrosive-free and ventilated indoors AC Power Supply Voltage 100-240 V～ Frequency 50/60 Hz Current...

  • Page 60: Hardware Specifications

    A.3 Hardware Specifications A.3.1 Display Display Type Monochrome LCD Size (diagonal) 3 inches Differentiation 128 pixels A.3.2 Battery Internal battery No. of batteries 1 (standard) or 2 (optional) Battery type Lithium battery Shutdown delay At least 30 mins (new battery, after the first low battery alarm) Battery voltage 7.2V Battery capacity...

  • Page 61: Auditory Indicator

    A.3.4 Auditory Indicator Produce an alarm, the sound pressure is dB(A) and key 56-80 Speaker beep; Support multi-level volume functions; The alarm sound meets the requirements of the IEC60601-1-8. A.3.5 External Ports Ports AC power supply One AC power supply port port Multifunction One multifunction interface with the following functions:...

  • Page 62: Specifications

    A.4 Specifications Parameters Specifications Factory Default Syringe used in conjunction with syringe pump should meet the requirements of Syringe standard ISO 7886-1: Sterile hypodermic syringes for single use. Compatible syringe 5ml, 10ml, 20ml, 30ml, 50ml/60ml sizes  5ml syringe: 0.1-150ml/h ...
  • Page 63 5 Levels are adjustable, respectively are: 75± 50mmHg (10.0± 6.7kPa), 150± 125mmHg (20.0± 16.7kPa), 300± 125mmHg (40.0± 16.7kPa), 525± 125mmHg (70.0± 16.7kPa), 900± 180mmHg (120.0± 24.0kPa). Maximum occlusion pressure is about 1080mmHg. Note 1: The detected pressure of the infusion system (syringe pump and Pressure 525mmHg syringe) is affected by inner diameter,...
  • Page 64 BW Mode Conc., Drug Amount and Volume Conc. Configuration Drug Library On, Off Para. Memory On, Off Time:_ _:_ _ 00:00 Date:_ _ _ _-_ _-_ _ 01-01-2018 Date and Time Time format: 12h, 24h Date format: yyyy-mm-dd, mm-dd-yyyy Domestic: yyyy-mm-dd or dd-mm-yyyy International: dd-mm-yyyy You can select language according to...

  • Page 65: A Reference Table Showing Occlusion Alarm Delay And Possible Dose

    A.5 A Reference Table Showing Occlusion Alarm Delay and Possible Dose Occlusion Pressure Rate Time of Occlusion Alarm (mmHg) (ml/h) (hh:mm:ss) 01:16:01 00:08:35 00:06:00 09:11:42 00:53:13 00:15:00 Rate Pressure Setting Bolus Volume (ml) (ml/h) <0.2 <0.332 NOTE  Test conditions: ...

  • Page 66: Infusion Accuracy Curve

    A.6 Infusion Accuracy Curve The following typical infusion accuracy table expresses performance after infusion has started and infusion fluctuations occurring within a certain period of time after normal infusion flow volumes have been reached. The infusion accuracy table is for reference only;...

  • Page 67: Trumpet Curve

    A.7 Trumpet Curve Flow rate deviation over time (p△t) Syringe brand: B.Braun Original Perfusor Syringe Syringe specification: 20ml Sampling quantity of pump: 3 Sampling quantity of syringe: 3 Sampling rate: 1ml/h Sampling interval: △t =0.5 min Observation windows: p△t = 2, 5, 11, 19, 31 mins Maximum deviation over the course of a full observation window: EPmax (%) Minimum deviation over the course of a full observation window: EPmin (%) Average deviation: A (%)

  • Page 68: B Emc And Radio Regulatory Compliance

    EMC and Radio Regulatory Compliance B.1 EMC The device meets the requirements of IEC 60601-1-2:2014. NOTE  Use of accessories, transducers and cables other than those specified or provided by the manufacturer of this device could result in increased electromagnetic emissions or decreased electromagnetic immunity of this device and result in improper operation.
  • Page 69 Guidance and Declaration - Electromagnetic Emissions The device 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. Emission test Compliance Electromagnetic environment - guidance Conducted and radiated Group 1 The device uses RF energy only for its...
  • Page 70 If the device is operated within the electromagnetic environment listed in Table Guidance and Declaration —Electromagnetic Immunity, the system will remain safe and provide the following essential performance:  Operating mode  Accuracy  Function  Protection against UNINTENDED BOLUS volumes ...
  • Page 71 power supply or a battery. RATED power 30 A/m 30 A/m Power frequency frequency 50 Hz / 60 Hz 50 Hz / 60 Hz magnetic fields should magnetic fields be at levels IEC 61000-4-8 characteristic of a typical location in a typical commercial or hospital environment.
  • Page 72 9 V/m 9 V/m electromagnetic site survey , should 704–787 MHz, be less than the compliance level in 5100–5800 each frequency range Interference may occur in the vicinity of equipment marked with the following symbol: Note 1: At 80 MHz and 800 MHz, the higher frequency range applies. Note 2: These guidelines may not apply in all situations.

  • Page 73: Radio Regulatory Compliance

    Recommended Separation Distances between Portable and Mobile RF, Communications Equipment and This Equipment The equipment is intended for use in an electromagnetic environment in which radiated RF disturbance 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 communication equipment.

  • Page 74: C Alarm Information

    Alarm Information This chapter presents the alarm information of the syringe pump. Prompt information for operation guidance will not be presented in this chapter. The table shows the appropriate countermeasures for each piece of information related to alarm triggering. If the problem still exists after operating according to the countermeasures, please contact the company.
  • Page 75 Check and eliminate the Syringe is disengaged source of the alarm, [Syringe during infusion. Infusion is High Disengaged] stopped after the alarm is press to cancel triggered. alarm. Power supply voltage Alarm cannot be abnormal (overhigh), AD cancelled. Please stop [System Error] High value of sensor abnormal,...
  • Page 76 1. The alarm will not be cancelled automatically until the infusion is completed, and then switch to [VTBI Complete] or [Syringe Infusion remaining time Empty] alarm. [Time Near End] reaches the setting value of [Time Near End]. 2. Or press cancel alarm.
  • Page 77 Syringe pump and BeneFusion CS5 Infusion Supervision System are communicated Press or restore successfully over Wi-Fi, the communication the network [Communication between syringe communication is interrupted] pump(s) and abnormally interrupted for BeneFusion CS5 3 minutes. After the alarm Infusion Supervision is triggered, infusion of the System.

  • Page 78: D Symbols And Terms

    Symbols and Terms D.1 List of Units Abbreviation Meaning ampere ℃ centigrade centimeter decibel gram hour hertz inch inch kilo kilogram kilopascal litre pound meter milligrams minute milliliter millimeters mmHg millimeters of mercury second μg Microgram volt volt ampere watt...

  • Page 79: List Of Symbols

    D.2 List of Symbols Symbols Meaning minus percent Per; divide; or ～ power plus ＋ ＝ equal to < less than > greater than ≤ less than or equal to ≥ greater than or equal to plus or minus ± ×...

  • Page 80: List Of Unit Conversion

    Abbreviation Meaning European Economic Community Electromagnetic compatibility Electromagnetic interference C2H4O Intensive Care Unit Identification International Electrotechnical Commission IEEE Institute of Electrical and Electronic Engineers International organization for Standardization Keep vein open Light emitting diode Maximum Medical Device Directive Minimum Magnetic resonance imaging Not applied NICU Newborn Intensive Care Unit...

  • Page 81: E Toxic And Hazardous Substances Or Elements

    Toxic and Hazardous Substances or Elements Cr(VI) PBDE Name of the Parts Cr(VI) PBDE ○ ○ ○ ○ ○ ○ Front housing ○ ○ ○ ○ ○ ○ Back housing Device ○ ○ ○ ○ ○ ○ Keys housing ○ ○...

  • Page 82: F Declaration Of Conformity

    Declaration of Conformity P/N: 046-013104-00 (4.0)

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