V Series Infusion Pump User Manual
Contents
1. y A amp AL O SS f Ss 49 4 Ten Bi The name of all parts for infusion pump behind 1 USB interface is used for the connection of other device Reserved Interface 2 Drip sensor is used to detect the status of liquid drip inside the Murphy s dropper of IV set and count the liquid drips splashed into the Murphy s dropper 3 The fixation clamp is used for fixing infusion pump onto the infusion stand or bedstead 4 Fixation handle Rotating and adjusting the fixation which it is lock or release 5 Power supply interface is used for the connection of AC power supply 6 DC 15V power output interface is used for output DV15V power supply 7 RS232 interface is used for external communications 8 DC12V Power input interface is used for the connection of 12v external DC power supply 9 Calling nurse interface is used for the connection of nurse calling system 2 6 Standard RS232 Interface The pump has a standard RS232 interface and it is communicated each other RS232 connected line is asked to use shielded wire an it should be accord with the standard request of information technique and safe standard for GB4943 2001 For more detailed information Please ask our company to the RS232 interface agreement The device must be connected with the specified equipment 13 2 7 Multi Channel Injection It is recommended that the infusion device use a one way valve under using mu2. The pipeline of infusion apparatus is Recheck the pipeline of infusion The Occlusion tied or the roller clamp is not opened apparatus alarm frequently l The pressure level is set too low Increase the pressure level occurs in the The pressure testing system has a Contact the manufacturer for infusion process failure warranty service Usually the product should be sent back to the company for maintenance if malfunction occurs within the one year defect warranty period and the company will take care of the entire maintenance cost and 37 delivery fee Serious Damage caused by carelessness of operator service cost can not depend on the manufacturer completely Battery is not in the range of the warranty spare part list If there is PO the condition 1s subject to the PO The company will provide designated and qualified technical persons with files listed in GB9706 1 6 8 3C Plus it is advised that the service time not exceeds 8 years over service life may increase the potential danger in the usage since the apparatus gets old 6 Maintenance O The pump should be regularly cleansed with clean wet cloth and appropriate amount of detergent then cleansed with clean wet cloth upon the external surface and finally with clean cloth to dry the surface and put on the dry shelf When battery is low the pump will give off intermittent alarm please charge the pump timely or connect the pump with AC power sup
3. physical and metering shall acquire verification and certification by relative supervision departments Warning Suggest use the IV set specially for the infusion pump other wise can not assure the injection accuracy Warning tube line of IV set will act poor rebounding performance or even have leakages after a while of usage thus after 6 hours continuous work the infusion pump shall be turned off and have the tube lines in slight motions in order to assure no extrusion unto the tube lines between the pump tablet and the pressing plate Warning when reinstalling the infusion tube infusion tubes that have been extruded shall not be located at the position of air bubble sensor otherwise it can cause error alert about air bubbles in the tubes Warning the roller clamp of infusion apparatus should be located onto the tube lines between the infusion pump and the patient when installing the infusion IV set Warning air bubbles in tube lines between the pump and the patient cannot be detected 1t has to be excluded manually Warning do not press hard the stress point of pressure sensor otherwise the press sensor will get damaged Warning the pump should not be operated by patient s family members in case incorrect operation brings about dangers to patients 36 Warning the rechargeable battery inside the pump should be examined upon its time length of charging and discharging every three months to prevent work fai
4. 3 3 Expected Suitable Object Used for the drugs injection for adult pediatric neonatal etc used in Infusion therapy 2 3 4 Expected User The doctor nurse or trained qualified medical staff in the hospital 2 3 5 Taboo 1 Taboo drugs insulin is not suitable for infusion pump injection 2 This product is strictly prohibited for blood transfusion 2 4 Technical Characteristics and Parameters 2 4 1 Rate Range of Adjustment 1ml h 1500m1 h When the speed is at 1 99 9 ml h the flow rate of infusion increases by 0 1 mL When the speed is above 100 mL h the flow rate of infusion increases by 1 mL h Measuring equipment calibration unit ml h 2 4 2 Accuracy Flow rate accuracy less than 5 after calibration accuracy can reach within 3 2 4 3 Purge Rate 200ml h 1000ml h Adjustable 2 4 4 Delivery Search 0 1ml 9999 ml Below 100ml the accuracy is 0 1ml Above 100ml the accuracy is 1ml 2 4 5 Delivery Limit 0 1m1 9999ml Adjust step 0 1ml Above 100ml the step is 1 ml 2 4 6 Occlusion Alarm Level Infusion pump obstruction pressure s setting range is 100mmHg 900mmHg 13 3kPa 120kPa Adjustable ten level error is 5OmmHg or 25 6 6kpa the bigger should be taken 2 4 7 Bubble Detector Ultrasonic detection method bubble above 25ul can detected 2 4 8 KVO Rate 1 5ml h Adjustable the default value is 2m1 h 2 4 9 History Record This series products can store more than 1500 historical r
5. nozzle and liquid level and try to keep the Murphy s dropper in the vertical position so that the drip sensor can accurately detect the status ofthe liquid drip inside the Murphy s dropper see Figure Figure Schematic Diagram for Installation of Drip Sensor Under using as the step above clean up the air which the infusion set is full and install it onto the infusion pump Warning Before the infusion install the user must clean up the air in the infusion to avoid the air admission Warning the infusion bottle or bag should be placed 20cm 80cm higher than the patient s heart Causion The infusion tube must near Pump Fingers eo After close pump door Press Bolus Button to clean up the air in the infusion tube Release the hands upon the medical liquid flow out e When all the parameter is setting completely inserted the needle into the patient s vein Press Start Button again to enable start the infusion AN Warning Before using the device The user must clean up the air in the infusion tube to avoid the air admission which may do harm to the patients 3 5 Selection of Infusion Mode There are totally five optional modes for infusion with the pump which are Speed Mode 17 Drip Mode Body Weight Mode Time Mode and Infusion Plan Menu In the state of pause press sum to enter the setup interface as shown in Figure 1 Speed Mode 2 Drip Mode 3 T
6. 50 60Hz Safety Class Class I Ipx4 Rated Power 28VA pe E a Sino Medical Device Technology Co Ltd Add 6th Floor Building 15 No 1008 Songbai Road En Nanshan District Shenzhen P R China ec ner Shanghai International Holding Corp GmbH Europe Add Eiffestrasse 80 20537 Hamburg Germany Product Name Infusion Pump Voltage 100V 240V 12V Product Model SN 1600V Power Frequency 50 60 Hz Safety Class Class I W IPx4 Rated Power 28VA pe E Sino Medical Device Technology Co Ltd Add 6th Floor Building 15 No 1008 Songbai Road Shanghai International Holding Corp GmbH Europe een NE ny C Enz Nanshan District Shenzhen P R China Add Eiffestrasse 80 20537 Hamburg An A Figure 1 4 3 3 SN 1600VR Label 2 Product Introduction 2 1 Overview Microprocessor based accuracy control Figure 1 4 3 4 SN 1600V Label motor as well as the pump tablet of drive finger press type peristaltic pump shall be applied in V series infusion pump to enable the medicine to be injected into the patient body with uniform speed accurate and safe dosage During the clinical treatment Vseries infusion pump is applicable to internal medicine surgery pediatrics obstetrics and gynecology ICU CCU ward and other clinical infusion therapies Note This product is strictly prohibited to be used in blood transfusion Main features are l
7. After the IV set brand indicates the calibrating status of IV set if there s 1t means the IV set haven t been calibrated otherwise it s calibrated 3 7 Advanced Parameter Setup Menu ax Return e On the pause condition press and enter into the setting page then press the System Enter setting and press SEES to enter such as the following picture In this page you can set the parameters ofthe KVO Bolus Rate Drip Sensor Switch and also the pressure level 1 Speed Mode 2 Drip Mode 3 Time Mode u Weight Mode 5 Infusion Plan 6 System Setting System Setting Page 21 1 Keypad Sound l 8 History Query ME 2 Sound Volume mM 9 IV Set Parameter 3 Pressure 6 10 TimeSetting 4 BedNumber 85 11 Drip Sensor off 9 Bolus Rate 600ml n 6 KVO 2mil h State Indicator on Parameter Setting Page 3 7 1 Keypad Tone Setup Once on the page of parameter setting when the Cursor stop at the keypad s sound and press A Vv or Gee to switch on or off the keypad sound 3 7 2 Alarm Tone Volume Setup Enter A Pros and put the cursor onto the alarm sound volume and press tum or UA to adjust the alarm sound volume level there are total three levels which can be adjustable 3 7 3 Pressure Alarm Limit Setup Enter A 6 Press Ca and put the cursor onto the Occlusion Level then press or to adjust the Occlusion level there are total ten levels which can be adju
8. G PRON 22 6 2 POVON O AS 6 2 2 Designations Represented Dy Models iia A cai 7 2 3 Operating Principle and Range of Application oooccccccnnncncnnncnnnnnnnncnnncnnncnnannnannnanann corro nnnnn nooo 7 23 1 Operating Prneple A A as E E ETO 7 23 2 IN E Sssreene 8 2 33 Fxpected SUA DLS ODE il 8 AI O 8 2232 LADO ao 8 2 4 Technical Characteristics and Parameters ococcnooococncnnnnnonononnnnnnnonnonnnnnnnonnnnnnnnnnnnnn noo nn ernennen 8 Ae ie o e 9 2 A Denver Searches RE 9 e En 9 24 6 Occlusion Alarm Level ee et 9 2437 DUDO Deister nannten a 9 ZA TR NORA ee ee ee 9 229 WALSTON INS COM er nee 9 DIN OPM At sists A 9 RO 9 2412 Environmental 10 24 13 Dimension cade 10 ZA o A 0 a ee 10 De Supported A A 10 2 3 External ND eA TANCE LS UCI ne Re 10 AS RS2 2 ls A A A ses 13 221 Mult Channel Injectich au een 14 OPERATING METHODS ui a aa 14 3 1 Pump lis tala thon ses 14 32 POWT ON ee east 15 3 3 Power On Off and System Self testenn ii 16 3 4 Installation of Infusion Components aa ae 16 3 3 8elec110m501 In fusion Mode nun Beenden En 33 1 Speed Modes elle ae 18 33 7 Da Mode nee ee Nee 19 O DPO Weiche Mode re ee 20 3 34 Time Moderna nern een ee ti 21 I HU 10 A ae 22 3 6 In1us1on Parameter Se ya eisen ss 23 SA elle 23 3 6 2 Preset Volume gt Diaria 24 e VOme EIT A ne 25 3 6 4 Pressure Alarm Limit Quick Setting ocoonccnccnonooooooooonnnnononnnnnononnnnnnnnncnnccnonncnnnonccnnccnannn 25 0 IV SetParameter Sel
9. GURATION 2 0uess ee 41 9 RELEVANT INFORMA TION aisscescassesnasonsenssesgesaaisoctswesnnssesvasscowsseseesesetasassbeekaeheesdseossessoseeosoabennce 41 1 Safety Information 1 1 Stipulations in the Manual The following information is applied in this manual to emphasize the hints on the messages relating to patients or devices or the potential risks Caution Be used to remind the situation in which the device or environmental damage may be caused Warning Be used to remind the situation in which injury or death may be caused Attention Be used to highlight the important guiding information which may have impact on how to use this manual and the product or used to provide some additional information such as detailed explanations hints or reminders 1 2 Safety Overview In accordance with the electrical safety classification V Series Infusion Pump falls into Category I CF type application part continuous operation equipment portable and IPX4 devices with internal power supply The following is an overview of safety precautions Operating personnel shall not be allowed to open the outer housing of device under any circumstances It is not allowed to let the security function components of built in device in a failure or short circuit condition If the device fails to operate normally it is not allowed to carry out repairs on your own Instead you should immediately contact with Sinomdt s qualifie
10. LED If the current rate is above KVO rate the infusion rate will be as preset KVO rate otherwise will be as the preset infusion rate 4 7 Alarm of KVO Completion In the KVO mode pump stops working with audible and visible alarm when the output dosage reaches 6ml the panel shows KVO FINISHED the alarm sound is not removable Note Infusion dosage of KVO will be counted into the accumulative dosage 4 8 Alarm of Drip Sensor Abnormality This alarm is only available when the drip sensor is used in rate mode or the drip mode is selected If any abnormality is detected by the system there will be an alarm with sound and light and t the led will display Drop Error You can press the silence button to remove the alarm sound Note Check if the installation drip folder is abnormal or not or whether bottle is empty or not 4 9 Alarm of Power Supply Breakdown Power supply switches on 1f without outside power supply connection or with electrical cord disconnecting in the course of service pump will give off intermittent alarm sound There will be note on the LCD to indicate the net electricity 1s off Pressing the silence button and the alarm sound can be removed 4 10 Alarm of Under Voltage Battery 1 When the battery is low light flickers one grid flickers pump will give off intermittent alarm sound this sound can be removed by pressing the silence button 2 minutes later it alarms again Meanwhile the pump can susta
11. Songbai Road Nanshan District Shenzhen P R China Zip 518055 Tel 86 755 86142985 Fax 86 755 86142985 Website www Sinomdt com Email information Sinomdt com Production License Number YSYJXSCX No 20061349 EC Representative Shanghai International Holding Corp GmbH Europe 41 Add Eiffestrasse 80 20537 Hamburg Germany Tel 49 40 2513175 Fax 49 40 255726 E mail shholding hotmail com 42
12. V Series Infusion Pump User Manual Version 0 2 Sino Medical Device Technology Co Ltd Declarations The information contained in this manual is based on the experiences and knowledge acquired by Sino Medical Device Technology Co Ltd Hereinafter referred to as Sinomdt from the product field Sinomdt is convinced that the information provided in this manual is accurate and reliable But we could not make any guarantees for the contents of this manual As this manual is only used to provide the guidance for the use operation and maintenance of infusion pump Sinomdt shall not assume liability for the property damages or personal injuries caused by the citations of the contents of this manual for other purposes This manual copyright is owned by Sinomdt and no reproduction or dissemination of its content and information is allowed without the prior written permission of Sinomdt The contents of this manual are subject to change without notice due to product upgrades or design improvements Before the installation and application of V series infusion pump please read this manual carefully Contents SAFETY INFORMATION 5 A A A 1 1 1 Stipulat ons n the Man AA Bat eweus l E Were ee ee ee reale l La Electrical Mechanical Safely una ee 2 BL EEC Sally onne era ee 2 oe A N 2 LA Symbols nd Labels aa 4 k ISa Symbol Se A A A eee 4 142 Transporte symbol taria 5 LE Product Labels ee 6 2 PRODUCT INT ROD U
13. am and return J 10 Confirm Button Select Button Select the program and enter it Shift the parameters on the some interface to select the parameters 11 Purge Button Press the key and press it again for 5 seconds Start the purge function Release the 11 key to enable to stop it 12 Silence Button Clean Button To be used for buzzer on silencea after alarm Enter the parameters Reset the infusion amount 13 Start Button Pause Button To be used for start or pause the infusion 14 Tubing clamp Clamp the pipeline after the pump gate is opened to avoid the excessive output of liquid medicine 15 Jacklight To be used for nighttime illumination 16 Occlusion Sensor Detect the pressure in infusion tube line 17 Pump Fingers Extrude the pipeline enabling the liquid to be drained from the infusion components 18 Pump Door Fix the infusion tube line components to be mounted 19 Door Handle To be used for the opening and closing of pump gate 20 Pressure Plate Use constant pressure to hold down the pipeline of infusion components 21 Bubble Sensor Detect the air bubble in infusion tube line 22 Drip Sensor Detect the drip 23 Infusion State Indicator Alarm Indicator The difference status For examples the infusion status alarm status and so on the indicator light can show different status and the indicator color 12 Wi w it A MAN VVVNVY VVVY VANS BE A AI
14. appear Re calibrate To ensure the accuracy of the calibration please return to the main page set the rate at 200ml h and Preset volume at 10ml for the testing to check whether you get your required mount of the liquid 10 ml in the testing cup 30 Brand lv2 Specification 20 Test Rate 200 ml h Test Vol 10ml Precision 80 otop when VOL reached IV Set calibration page Attention If there appear on the back of IV set brand that means the current used IV Set has not been calibrated and if there appear U01 that means the current used IV set has already been calibrated Attention If one hospital used the same brand of IV set it is more convenient for the IV Set calibration That is when you calibrate the IV set in one unit of the infusion pump and record the calibration number and when you calibrate the same IV set to another unit of infusion pump you just input the calibration number to the infusion pump after that the calibration is ok 3 7 10 Time Setup Move the Cursor to the time setting and set your required time details is as the following YEAR 2012 11 20 TIME 14 40 Time setup Interface Once enter into this page you can set the local time and the date as you require with the numeric 31 keypad and the button Enter and press Menu to confirm your set pareameter Select Return ef nf 3 7 11 Drip Sensor Switch Setup A Vv Move the Cursor to the Drip sensor sw
15. c pump control system and operation display system The finger press type peristaltic pump comprises motor tape handler peristaltic cam wiggle cam extrusion pump tablet and press plate At the time of operation the micro processing chip controls the rotation of motor and drive the peristaltic shaft to rotate after the deceleration of tape handler The peristaltic shaft drives the peristaltic cam to rotate enabling extrusion pump tablets to conduct regular up and down movement under the extrusion of cam The extrusion pump tablets alternatively extrude the infusion tube mounted between the press plate and extrusion tablet and subsequently push the liquid medicine to move forward The control system consisting of dual CPU chip motor control module and so on is applied to accurately control the flow rate of infusion and monitor the infusion status so that the safe and reliable infusion process can be guaranteed in the entire process The operation display system consisting of LCM control panel etc is applied to realize the man machine interaction and facilitate the operation of medical staffs 2 3 2 Expected Purpose V series infusion pump is adapted to the hospital department of internal medicine surgery pediatrics obstetrics and Gynecology ICU CCU room and other clinical infusion therapy Note This product is strictly prohibited for blood transfusion This product should operated by qualified workers in hospital 2
16. d Warning The application of inappropriate or misaligned IV set may cause inaccurate speed or dosage and subsequently do harm to patients Warning We recommend to use the special IV set for pumps for injection and We can not guarantee the accurates for other IV sets Warning In order to ensure the injection processing suggest to use the drip clamp Warning this pump use the principle of extrusion to creep do not use for blood transfusion Warning Keep attention to avoid the air into the patient when use this product Warning This product is not suitable for hyperbaric oxygen chamber and MRI inspection room Warning When using this device attention should be paid to avoid the air admission which may do harm to the patients Warning In order to prevent the producing of the overspeed in the infusion the users are suggested to connect the drip sensor with the host well before using of this product Caution Keep the environment clean and avoid shocks Keep away from the aggressive chemicals dusts high temperature and humidity environment Caution Electromagnetic interference Make ensure that the installation and service environment of this instrument are not subject to strong electromagnetic interference such as wireless transmitters or mobile phone interference Attention The protective cover should be arranged in place provided that RS232 interface of device is not in use Attention Tab
17. d personnel authorized to repair the equipment No repair parts meeting your needs are available inside the equipment Comply with all the warnings and attention hints whether it is clearly defined or self evident Follow the stipulations specified in all safety labels on the equipment 1 3 Electrical Mechanical Safety Only those well trained and qualified maintenance personnel authorized by the Sinomdt can open the outer housing of device and replace the electrical and mechanical components Otherwise problems of device safety may be caused The following is an overview of warning message 1 3 1 Electrical Safety Warning Risk of electric shock In order to protect patients and medical personnel it is necessary to make sure that proper grounding of equipment is arranged and protective grounding of power outlets remains intact It is prohibited to have the triaxial cable of this device connected to twin wire socket Warning Risk of electric shock It is prohibited to open the outer casing of device during the operating process or power connection Only authorized maintenance engineers are allowed to open it Caution Before use the user must check and make sure that there are no obvious damages which may have impact on the patient safety or equipment performance The recommended cycle of detection is once a week or a shorter period of time It is recommended to replace the damaged parts before use if obvious damag
18. ecords Automatic record key operations and event information after system booting including infusion start time accumulation flow rate state etc 2 4 10 Alarm In order to ensure the safety of infusion this series products with the following warning or reminding function over time not calibration occlusion bubble door open finish KVO completion drip sensor abnormality power supply breakdown under voltage battery battery running out system error Detailed information see Alarm Presentation 2 4 11 Power Power supply voltage A C 100V 240V D C 12V Power frequency 50 60 Hz Battery voltage DC 12V Battery working time under full charge condition Equipment can work more than 8 hours with a speed of 25ml h Maximum power 28VA Mode of operation continuous operation with intermittent loading Note Before first use battery charging time should reach to 12 hours 2 4 12 Environment Working environment Temperature 5 40 C Humidity 20 90 Transportation and storage condition Temperature 20 55C Humidity lt 95 2 4 13 Dimension 129mm X 130mm X 215mm 2 4 14 Net Weight 1 8kg 2 4 15 Supported Brand The infusion pump can record 12 different manufacturers IV sets 20 drops of ml 60 drops of ml included the 12 manufacturers were Ul1 U2 U3 U4 U5 U6 U 7 U 8 U 9 U 10 U 11 U 12 U XX number of IV set should pass the calibration function then the corresponding IV
19. ection iii td 26 3 7 Advanced Parameter Seupassi as ai 27 She KEDA OMe 19 a een A a ale 28 LAA one Voume AUD AAA 28 Jef 5 Ns An 28 3 74 Bed Number SCID sn 28 3 553 Bolus RAE UA ann IE eisen 28 TOR VOL AUC SOUND ee Bere en ee een 29 3 1 1 Operatine Light Switch Setup gt nass latas 29 37 8 a A sein 29 AN A 30 37 10 A E ae aS 31 3 1 11 DEP Senso Switch Sep a 32 3 8 Bolus PUM CIM ri nmesiee 32 3 9 Eishtins Function sa ek 32 3 10 Communication with Main Unit uses aa a 33 3 11 Management of the Battery RECIO are 33 O ee 33 A PO o eee Pee eed 33 ds ALARM PRESENTATION out eaceondetavueatt 34 Al A lari CENOWO PTA A A 34 42 Alam OT Not C ab ta ON ti dt 34 4 3 Alar 01 OCElu SION sacaaieeana naa ve uiuc Aclaseloawiaanl fad teaahcalecetslesaloscneceeat endsiecoeavauneavadeotnanseueaons 34 Ah A PS VANTIN Bubble ae ee O 34 AS Alarn 01 Door Open 2 2 era Sea cise desea alec ia tinea 34 ANNO A ans tices sense a E E 34 A Varin Or KR VOC Ori dd 35 4 8 Alarm of Drip Sensor Abnormality 2 ee 35 4 9 Alarm of Power Supply Breakdown a az an i esd besos 35 4 10 Alarm of Under Voltage Batter roerien e a a a 35 AELA hmot Battery Rune UE a A pag ae ene 35 4 12 Alarn of System Error a A A AA 35 5 ANALYSIS OF MALFUNCTION AND TROUBLESHOOTING s 00000ssrrr0000ssssssonoosrsenne 37 0 MAINTENANCE aaa 38 ENATURES OPTNEFUSTON 2 22 53 38 dl Namrec or Rate ACCUTANE 38 7 2 RESPONSE to OCCIUS MA A A A AS 40 SS BFANDARDEONEFI
20. es are found out Caution Periodic safety tests of the instrument should be conducted to ensure the safety of device The tests include leakage current measurement and insulation tests The recommended test period is once a year or the tests can be conducted in accordance with regulatory requirements and inspection procedures Caution Prior to the cleaning the power cord should be removed Use soft brush or soft cloth to wipe off the dust on the surface of device use brush to remove the dust on the connector or the edge of panel or use soft cloth soaked with neutral detergent cold disinfectant or 70 alcohol and isopropyl alcohol to wipe off the dust It is not allowed to let the detergent or disinfectant permeate into the internal part of device Special attention should be paid to the connectors edge of panel and other locations 1 3 2 Application Safety Warning It is prohibited to operate this device beyond the limits for operating environment Otherwise the device may be caused to operate abnormally The operating environment is defined as follows Operating temperature 5 40 C Relative Humidity Relative humidity 20 90 Atmospheric Pressure 86kPa 106kPa Supply Voltage 100 240 V 50Hz 60Hz 12V Rate of Power No more than 28VA Warning Not suitable for the operation under the environment in which oxygen and nitrogen oxide flammable anesthetic are mixed Otherwise explosion may be cause
21. etting useless because of auto discharging Promptly connect the pump with AC power supply for charging or turn off the pump when alarming the energy run out otherwise energy run out may do harm to the battery Ineffective battery should be taken to the place designated by environment protection sections or sent back to our company for unified disposal to prevent environment pollution 3 11 2 Recharging Battery recharging of Sinomdt pump is both available at both turn off and turn on conditon stop recharging once full During the process of battery recharging firstly at constant current charging and then constant voltage charging switch to trickle recharging close to saturation stop recharging once full 33 4 Alarm Presentation 4 1 Alarm of Non Operation Alarm turns on when no operation proceeds after the device starts up or service suspends for 2 minutes meanwhile the lcd will display NoOp the alarm sound can be removed by pressing the SLIENCE button 4 2 Alarm of Not Calibration If the pump doesn t run with unaligned infusion apparatus after pressing the START button the main interface will display NOT CALIBRATED The troubleshooting method replace with an aligned infusion apparatus or enter the calibration interface to align the infusion apparatus for details of aligning infusion apparatus please refer to Section 3 7 9 4 3 Alarm of Occlusion In the course of infusion when the pressu
22. he Rate of 1 ml h 30 nl h r WW Tiwana i an AA Fur Ge T AA river AA AAA Ca ae A ao aU 13 10 120 min 30 B 30 39 Rising Curve at the Rate of 25 ml h 10 10 2 5 11 15 31 min Trumpet Curve at the Rate of 25 ml h Warning The above testing result is the one used by the IV set 20 drop ml So that there will be some small difference if used other brand of IV Set for the testing 7 2 Response to Occlusion The occlusion alarm time is a main indicator of the nature of response to occlusion In this test use 20 d ml apparatus the following data only present the results of the test about the infusion apparatus used in the test Note The response time of occlusion alarm is subject to the infusion rate infusion apparatus brand pressure level etc Flow rate Occlusion alarm Occlusion Response time of ml h pressure alarming OhOmin3 sec OhOmin6sec 40 500 0h31min25sec CONEA p Dose caused by the occlusion alarm the testing is used with IV Set 20drop ml brand at the rate of 25ml h if the occlusion set at the first level the dose is 0 06ml if the occlusion set at tenth level the dose is 0 2m1 8 Standard Configuration e Infusion Pump 1 PCS e Power line 1 PCS e User manual 1 PCS e Certificate of conformility 1 PCS e Warrantly card 1 PCS 9 Relevant Information Manufacturer Sino Medical Device Technology Co Ltd Add 6th Floor Building 15 No 1008
23. icator is on the pump is at the power on state Ifthe pump can t open and the current battery power is not enough the pump will automatical charge 3 3 Power On Off and System Self test After the external power supply is switched on the external power indicator AE is on the I pump is at the power on state At this moment press the K key for 1 second to enable the start up of device Under the premise that the internal battery is used the battery indicates the current battery l power after the power switch O is pressed to enable the start up of device The system starts to conduct self test after the start up of device At this moment the buzzing sound will be given out the indicator and alarm light will bright up according to priority and the pump will automatically check each of the functions Note All keys will be tested during the self test process In order to avoid an alarm for key error please do not press any key If there is no error message on the main interface of LCD screen after the self test that means the pump works normally At the moment the device is in standby state The pump will give out alarm if the system is in abnormal condition For this regard please refer to the description of alarm After the external power supply is switched on Press the key for seconds to enable switch off Start l device Under infusion status Press ause to stop infusion Press the key for seconds to enable s
24. ime Mode 4 Weight Mode o Infusion Plan 6 System Setting Figure Setup Interface A Enter 6 Select Bde ae RR Move the cursor to OF a pres to enter infusion setting interface Infusion mode can be shifted it can met different clinical application Incluing Speed Mode is fixed for all series pumps Drip Mode is fixed for all series pumps Time Mode is fixed for the pump model of SN 1800VR SN 1800V Body Weight Mode is fixed for the pump model of SN 1800VR SN 1800V Infusion Plan is fixed for the pump model of SN 1800VR SN 1800V 3 5 1 Speed Mode Select Speed Mode and the system automatically enters into the main interface of Enter speed mode shown as Figure Press Gele to enter the setup interface and shift t The Be numeric keypad can be set number parameters o can also set nonnumeric Start paramters The parameter have been set completely press Cause to start the infusion 18 Rate 00 ml h Preset 0 0 mi Flowed 0 0 mi 10 lv 2 M Speed 20 Figure Main Interface of Speed Mode 3 5 2 Drip Mode Select Drip Mode and enter its main interface If Drip sensor function is avtivated there will be an icon Ld r popped up on the right side of the interface shown as Figure Je Rate d min Preset 0 0 mi Flowed 0 0 ml 10 lv2 M Drip 20 Figure Main Interface of Drip Mode After select Drip Mode and en
25. in the service for 30 minutes longer at the rate of 25 ml h 4 11 Alarm of Battery Running out When the battery runs out of energy at the flow rate of 25 ml h only able to last for 3 minutes the pump stops working Light flickers with lasting noise of alarming which 1s not removable 4 12 Alarm of System Error Error operation or machine breakdown turns on the alarm noise and the SysErr lamp at the alarm 35 indicator with the main interface displaying the error code the reason for the error lists as follows here requires to re start the device 1f re start the device but the system remains alarming errors please contact the post sale service department Note When the above alarm happens the user can see it clearly at the distance of 4 m Occlusion Bubble Door Open Drip Sensor Abnormality System Error Power Supply Breakdown these alarms have been with first priority Infusion Finish with second priority other alarms with lower priority such as Non Operation Warning Warning the pump adopts the all extrusion peristaltic principle and it is prohibited to have the pump applied at the occasion of blood transfusion Warning IV set to be used must be precisely calibrated otherwise phenomenon as inaccuracy of the flow rate occlusion pressure error alert will happen As for designated infusion Set we only recognize its external structural size and the index as biochemical
26. isted as follows eA high degree of intelligence dual CPU chip and real time monitoring of the entire infusion process ensure a more secure and reliable infusion process e Wide range of infusion flow rate namely 1m1 h 1500m1 h e Wide range of application and suitable for 20 drops ml and 60 drops ml IV set e High bright LED lamp is applied to indicate the state of alarm so that the cal personnel can clearly observe the state of infusion from a distance of 5 meters e Lighting lamp inside the pump At night it can be automatically switched on to facilitate the operation at night of medical personnel as long as the pump gate is opened e History record The history records of more than 1500 previous infusions can be kept 2 2 Designations Represented by Models This series of products include the following Models SN 1800V Professional without wireless communication function SN 1800VR Professional with wireless communication function SN 1600V Basic type only support the speed mode and drip mode no wireless communication function SN 1600VR Basic type only support the speed mode and drip mode no wireless communication function In addition to the wireless communication function the specification of this 4 models is almost the same 2 3 Operating Principle and Range of Application 2 3 1 Operating Principle The pump falling into the category of volumetric type pump is composed of finger press type peristalti
27. itch setup press and Cue to set the switch When the injection is under Speed mode Time mode and Body Weight Mode as well as Infusion Plan the use can also be able to use this drop sensor which can check in time whether the whole process of the injection is right or not at the same time the sensor switch must be connected to the Moufi Tube When the function of drip sensor alarm is working or the infusion mode is drip mode there will Je appear on the top of the main page Jr Rate 0 d min Preset 0 0 ml Flowed 0 0ml 10 lt lv2 M Speed 20 Drip Sensor Page Note In Order to ensure the safety of the Injection suggest use this Drip Sensor alarm function 3 8 Bolus Function Purge function Bolus function can be performed both in the state of Pause and in the infusion process The purge dosage generated in the state of Pause is not accumulated to the infusion amount while the purge dosage in the infusion process is accumulated Bolus Press and then press it again within 5s and hold it to start purge 3 9 Lighting Function At night or the light is very dim in the room once you open the door the light inside of the pump SL will be on automatically which shall enhance the convenience of the operation 3 10 Communication with Main Unit By connecting to the main unit for communication the transfusion pump system can realize the data transfer with the main
28. lti channel injection If there is no one way value in the infusion tube and it happened to be able to detect the block for the patient and it can lead to the drug corner After release the block the drug corner will inject the patient with unknown speed It is very dangerous to the patient 3 Operating Methods The operating process of pump 1s listed as follows 1 Power on Bubble sensor 2 Open the door fitthe tube into the groove on bubble sensor hold the tube with tubing clamp and close the pump door TOBY dan u 3 Install the drip sensor between the nozzle of dropper and liquid level if use drip sensor alarm function or select the drip mode 4 Setup preset amount infusion rate ressure sensitivity etc Rate 0 0 mihi P y Preset 0 0 ml Flowed 0 0ml 5 Press the PURGE button to clean up the bubblesinthe tube 6 Stickthe IV set s needle into patient s blood vessel 7 Start infusion 3 1 Pump Installation e By rotating the fixation clamp at the back of device it is possible to enable the device to be fixed onto the infusion stand eWhen pump is fixed onto the vertical strut at first fixation clamp fixed onto the strut clamp the 14 strut and then rotating the fixation clamp and clamp the strut it will fixed onto the vertical strut alte a oe nee Sein ca A 3 2 Power On After the external power supply is switched on the external power ind
29. lure caused by run out of battery energy when it works relying on battery Battery s rated discharging time is 6hours yet under a damaged or incomplete charged condition the time length the battery supports the pump service is not certain Warning ineffective battery should be taken to the place designated by environment protection sections or sent back to our company for unified disposal to prevent environment pollution Properly handle the parts off the apparatus when repaired or when the apparatus s service life becomes due in order to avoid environment pollution Warning Used under the regular care of the nurse or other medical Persons Warning the IV set to be used with the pump must get the Medical Registration or CE And also the IV set have to be calibrated before first using otherwise inaccuracy will occur 5 Analysis of Malfunction and Troubleshooting No response when The battery voltage is too low and the Connect the AC power supply you press the power AC power supply is not connected and keep charging the battery button Power System has failure Send back to the factory The Drip Error l o l Reinstall the drip sensor The drip sensor is installed incorrectly message appears correctly frequently when the l Select a calibrated infusion The infusion apparatus is inappropriate drip sensor alarm l apparatus or recalibrate the o or not calibrated properly l l function is enabled infusion apparatus
30. o the actual amount of the liquid in the infusion bottle or infusion bag 3 6 3 Delivery volume clear Clear Move the cursorto Volume shown as Figure press Silence to clear the delivered volume Rate 0 0 ml h Preset 0 0 mi Flowed D mli 10 ly 2 M Speed 20 Delivered volume Setup 3 6 4 Pressure Alarm Limit Quick Setting A Vv Move the cursor to Pressure shown as Figure Press umm ummm to Set up the pressure level from 1 10 Rate 0 0 ml h Preset 0 0 mi 0 0 ml ve an AS Pressure level Setup 25 3 6 5 IV Set Parameter Selection A Move the cursor to Pressure shown as Figure Press ESES to choose the brand of IV set Move the cursor to IV set specification The number 20 60 following the brand indicates the specification of current IV set is 20 drips or 60 drips every milliliter shown as Figure Press A 3 by v v to choose the specification of IV set Rate 0 0 ml h Preset 0 0 mi Flowed 0 0 mi cones Speed Sery IV set brand setup Rate 0 0 ml h Preset 0 0 mi Flowed 00ml v2 20 10 M Speed IV set specification Setup Flow rate error may exist during the infusion process due to different thickness pipe diameter and 26 materials of the IV set from different brands and varying ambient conditions such as temperature and wetness So the IV set of a new brand or used in a new environment must be calibrated prior to its use
31. on time at beginning and lasting the whole system shall be able to store 1500 PCS of records if the records is full the old records will covered by the new ones Press gt and 6 to change the pages and the page number will Vv appear at the bottom of the screen 9 History Query 9 IV SetParameter 10 Time Setting 11 Drip Sensor off History Inquiry Interface 1 29 2012 11 28 21 00 Rate 0 0 ml h Preset 0 0 mi Flowed 0 0 ml Mode Speed State Open 2012 11 28 22 12 page History Inquiry Interface 2 3 7 9 IV Set Calibration Move the Cursor to the IV set Calibration enter into the IV Set calibration page select the brand of the IV set which needed to be calibrated if the brand of the IV Set not listed in the confirmed there are 12 brands for your selection such as U 1 U2 U3 U4 US5 U 6 And the size of the IV set should be 20 drop ml and 60drop ml use the confirmed parameter in the system for the testing please see the following Before IV Calibration please get rid of the air bubble in the tube put the out put part of the IV tube Start into the testing cup Press Ze and begin the IV set calibration When the liquid volume reach the Start desired one press cause to stop the testing if the testing is successful there will appear Testing Over at the screen After that the system shall calculate the relative calibration number And if the Error 1s too big there will
32. oo drug Insulin is not suitable for infusion pump injection since insulin should be kept at a low temperature Insulin should be injected quickly after leaving the low temperature environment Attention The IV set should fit with the National relative sanitation and quality standard for disposable goods do not crossed use after using the disposable IV set the operator should deal with it as the medical rabbish Attention Please use the power line battery from Sinomdt otherwise will possibly lead to irregular injection 1 4 Symbols and Labels 1 4 1 Safety Symbols On Off or power connection Functional grounding Protective grounding Hazardous voltage Access to random file CF Type Application Part Big Battery electric quantity Representative authorized by European Union Production date Serial number CE certification mark The marked numeric code stands for the code of certification authority Company Logo z mm 0001001014 o Anti water level 4 splash proof no bad infection when splashed by water from any direction Nonrecoverable mark Humidity Storage Condition It is not allowed to have the product exposed in the environment where the displayed humidity limit is exceeded 106KPa During transportation the atmospheric pressure shall be not more than 106KPa or less than SOKPa Temperature Condition It is not allowed to have the product exposed in the en
33. ply when the battery runs out of energy pump will stop work with audible and visible alarm please turn off the device immediately or connect with AC power supply to continue the service The charging method in the state of turn off connect the pump with AC power supply once the AC electrical indicator lamp lights up the pump are in the charging state Note recharge 12 hours continuously in the state of turn off With long time standby the pump should be charged every 3 months to prevent the inset battery from getting useless because of auto discharging With long time standby the pump should be examined upon the charging and discharging of the battery in case of black out condition when the inset battery is needed yet out of work if the battery is found malfunction with charging please contact our company to replace with new rechargeable battery unit Battery replacement should be operated by authorized personnel The replacing way 1s loosen off the behind screws open the behind lid take away the lead plug and then loosen off the battery box s screws take away the old battery and replace with the new one then plug the battery lead plug into the socket and finally fix the screws 7 Natures of Infusion 7 1 Natures of Rate Accuracy IV set type 20drops ml 38 Method Ways regulated by GB9706 27 2005 Testing result as follows Rising Curve at the Rate of 1 ml h 31 min 19 11 Trumpet Curve at t
34. re inside the infusion tube arrives at the set limit value alarm turns on with sound and light and the lcd will display Occl then pumps automatically stops working and releases the excessive dosage caused by occlusion pressing silence button can remove the alarm sound Exclusion examine ifthe infusion tube line twists or ties together 4 4 Alarm of Bubble In the course of service ultra sound air bubble sensor detects the bubble then alarm turns on with light and sound the lcd will display Bubb the pump automatically stops work pressing the Silence button can remove the alarm sound Exclusion clean up the bubble inside the infusion tube and insert the infusion tube into the bottom of the bubble sensor 4 5 Alarm of Door Open If the pump door is open when the pump is running there will be an alarm with sound and light t the led will display Open and the pump will auto stop working You can press the silence button to remove the alarm sound Exclusion check ifthe pump gate is closed properly 4 6 Alarm of Finish Infusion Upon the completion of the setting volume of infusion the system will automatically enter the 34 KVO keep vein open meanwhile with the audible and visible alarm the lcd will display Finish and KVO The alarm sound can be removed 2 minutes later the alarm works again press PAUSE to suspend the infusion process Note once in KVO mode KVO rate will appear on the
35. set can be use Warning If the IV set without calibration it may lead to inaccurate infusion User choose IV set should get CE certificate or get the allow for accessing into local medical equipment market 2 5 External Appearance Structure The main unit of infusion pump mainly consists of the outer casing pump gate operating panel peristaltic pump and drip sensor Its external appearance and structure is shown in below Figure 10 Ba N a 3 l TA RX lt 20 SSR Mo gt ie DL 6 mi L l i 8 ti MON Th 9 Se TIN EN 10 aan UE 11 12 137 14 18 16 17 18 The specific descriptions of all parts are listed as follows 1 System error Alarm Indicator used for alarm indication when system error occurred 2 AC Indicator the indicator lights up when connected to AC power 3 Power key long press to turn on off 4 5 Drip mode indicator Speed mode indicator drop mode is different with other modes in digital display unit it display lamp for displaying the current infusion data unit 6 LED Display to show the speed data 7 LCD Display to show the related data status alarm information etc 8 Numeric Keypad for inputting numerical information Number 3 and number 6 owns choosing upper or lower function When you entered 3 or 6 except in the situation for choosing upper or lower other situation only entered number 3 or number 6 9 MENU Buttom Return Button Select the menu progr
36. stable The relative occlusion parameter is as follows the range of the occlusion lever is 100mmHg 900mmHg 13 3kPa 120kPa ten levels to be adjustable and the Error is 50mmHg 6 6kpa or 25 3 7 4 Bed Number Setup Press Enter and put the cursor onto the Bed No then input the Bed number with the Numeric Select keypad the number is from 1 to 255 3 7 5 Bolus Rate Setup Enter Press ea and put the cursor onto the Bolus rate setting then input the bolus rate with the Numeric keypad 28 Attention Purge rate is from 200 1000ml h 3 7 6 KVO Rate Setup Enter Press ee and put the cursor onto the KVO rate setting then input the KVO rate with the Numeric keypad So that once the injection is finished the pump will go into KVO mode instantly Attention Range of KVO rate is from 1 Sml h 3 7 7 Operating Light Switch Setup Enter A 6 Press 22685 and put the cursor onto the Operation Switch setting and press OF ey to switch on or off the Operating Light Switch 3 7 8 Inquiry to Infusion History Enter A 6 Select l 3 Press and put the cursor onto the History Record and press or Select Enter between al and When it is on PR Press ene enter into the page of History Record such as the following picture The infusion pump will record some information during the process of injection such as Infusion rate preset volume Total volume infusion mode infusion condition infusi
37. ter the main interface of drip mode The label showed onto the Enter main interface Shown as figure Press Goes to select the parameter The numeric keypad can be set 6 number parameter cy can also be set nonnumeric parameters The parameter have been Start set completely press Pause to start the infusion Note Under Drip Mode the Murphy s tube must be clamped by the drip sensor because the drip sensor of infusion pump detects the liquid drops through Murphy s tube in real time 3 5 3 Body Weight Mode Enter Select Weight Mode and enter into its main interface Press eeu to select the a Parameters The numeric keypad can be set number parameters OF ger can also be set nonnumeric parameters DOSE Rate 000 ug kg min B WWEIGHT 0 0kg DRUG VOL 0 0mg SOL VOL 0 0ml M Veight Figure Body Weight Mode Interface Parameters after setting can be calculated into infusion rate that currently needed with following functions Dose Unit ug kgxmin DOSE ug kexmin xB WEIGHT ke xSOL VOL ml x60 Flow rate ml h DRUG VOL mg x1000 Dose Unit mg kgxh DOSE mg kgxh xB WEIGHT kg xSOL VOL ml Flow rate ml h DRUG VOL mg After the parameters are set system will automatically calculate corresponding rate and indicate it Enter on indicator Press ee to return to main interface of body weight mode At this moment Set 20 Menu the other parameters Press cam to re
38. this moment Set the other Menu parameters shown as Figure Press geum to return to the parameter setting of infusion plan under Start the main interface of infusion plan After setting up Press Ease to start infusion When the first plan is finished the system will automatically shift to the second plan to continue infusion When the second plan is finished the entire infusion process is completed Rate 0 0 ml h Preset 0 0 mi Flowed 0 0 mi 10 q 2 M Plan 1 Main Interface of Infusion Plan 3 6 Infusion Parameters Setup 3 6 1 Infusion Rate Setup Default position of cursor is on rate setup after turning on shown as Figure Use numeric keypad to set up the value 23 Rate 00 mi h Preset 0 0 ml Flowed 0 0 mi 10 lv 2 M Speed 20 Infusion Rate Setup Note the rate unit of d min can be only used under Drip Mode See Clause 3 5 2 for detailed introduction to Drip Mode 3 6 2 Preset Volume Setup Move the cursor to Preset shown as Figure Use numeric keypad to set up the value Below 100mL is accurate to 0 1mL over 100mL is accurate to 1mL Rate 0 0 ml h Preset 0O mi Flowed 0 0 mi 10 lv 2 M Speed 20 Preset Volume Setup The default value of Preset is 0 after turning on The infusion process will last until no liquid is left if the preset volume keeps unaltered preset volume is 0 Note Ensure the value of Preset Volume is smaller than equal t
39. turn to the parameter setting of body weight mode After Start Pause the parameter have been set completely press JE to start the infusion Rate 0 0 ml h Preset Om Flowed 0 0 mi 10 Iv 2 M We ght 20 Figure Main Interface of Body Weight Mode 3 5 4 Time Mode Enter Select and enter into the main interface of Time Mode shown as Figure Press ee to a shift the paramenters The numeric keypad can be set number parameters ig er can Start also set nonnumeric paramters After the parameter have been set completely press Cause to start the infusion 21 Set Time Oho m Preset Flowed 10 IM Time Figure Main Interface of Time Mode Different with other modes it is unnecessary to set the rate in calculated after setting the values of Preset indicator will automatically display rate value 3 5 5 Infusion Plan Enter the main interface of Infusion Plan Enter Select and 0 0 ml 0 0 mi Ivy 2 20 Set Time Time Mode Rate can be Note The infusion velocity to set two groups of rate and preset volume parameters shown as Figure Press to shift the parameters the numeric keypad can be set the number parameters Plant Rate Preset Plan2 Rate Preset M Plan 0 ml h 0 0 ml 0 0 ml h 0 0 ml Figure the main interface of infusion plan Enter Select After setting press mmm to return to the main interface At
40. unit As for that SN 1600V and SN 1800V can utilize standard RS232 interface to communicate with the main unit SN 1800VR and SN 1600VR support wireless mode and can also use RS232 interface to communicate with the main unit Notes standard RS232 interface can be used for two way communication where shielding cable is required and the device being connected shall comply with the requirements of GB4943 2001 Safety of Information Technology Equipment For more information please ask salesman from Sinomdt for RS232 Interface Protocol Device being connected must be the one specified by Sinmdt 3 11 Management of the Battery Recharging 3 11 1 Battery Type of the battery 12v 2300mAh 72 51 29mm With Thermistor Apearance of the battery There should be no deformation leakage and other defects Discharging voltage limited 10V Normal working voltage above 12V The rechargeable battery inside the pump should be examined upon its time length of charging and discharging every three months to prevent work failure caused by run out of battery energy when it works relying on battery Battery s rated discharging time is 6hours yet under a damaged or incomplete charged condition the time length the battery supports the pump service 1s not certain It should have 12 continuous hours for charging in turn off condition prior to its first use If long time standing by the pump should be charged every 3 months to prevent inset battery from g
41. vironment where the displayed temperature limit is exceeded Location This side up 1 4 3 Product Labels w 3 SINO MEDICAL DEVICE TECHNOLOGY CO LTD SINO MEDICAL DEVICE TECHNOLOGY CO LTD T www sinomdt com Product Name Infusion Pump Voltage 100V 240V 12V Product Model SN 1800VR Power Frequency 50 60Hz Safety Class Class I Y Ipx4 Rated Power 28VA m E Sino Medical Device Technology Co Ltd Add 6th Floor Building 15 No 1008 Songbai Road Nanshan District Shenzhen P R China ec ner Shanghai International Holding Corp GmbH Europe Add Eiffestrasse 80 20537 Hamburg Germany 0123 www sinomdt com Product Name Infusion Pump Voltage 100V 240V 12V Product Model SN 1800V Power Frequency 50 60Hz Safety Class Class I W Ipx4 Rated Power 28VA iia E Add 6th Floor Building 15 No 1008 Songbai Road Nanshan District Shenzhen P R China Shanghai International Holding Corp GmbH Europe Ec ner CE Sino Medical Device Technology Co Ltd Add Eiffestrasse 80 20537 Hamburg Germany 7 Figure 1 4 3 1 SN 1800VR Label 5 SINO MEDICAL DEVICE TECHNOLOGY CO LTD Figure 1 4 3 2 SN 1800V Label SINO MEDICAL DEVICE TECHNOLOGY CO LTD SINO MDT www sinomdt com www sinomdt com Product Name Infusion Pump Voltage 100V 240V 12V Product Model SN 1600VR Power Frequency
42. witched off device After power off the data stored in the memory chip is not lost due to power off 3 4 Installation of Infusion Components Make the infusion components ready Hang the IV bottle or bag onto the IV stand Note the infusion bottle or bag should be placed 20cm 80cm higher than the patient s heart open the package of IV set components and close the roller clamp of IV set After the infusion components are properly connected use your hands to extrude the Murphy s dropper of IV set and enable it to be filled with liquid An appropriate filling amount is one third of the Murphy s dropper Open the roller clamp fill the infusion tube with infusion liquid to exhaust the air bubble and then close the roller clamp Properly install the infusion tube Lift up the pump handle open the door start the installation from up to down smoothly insert the tube into the pipe clamp bubble sensor and tubing clamp according to priority After the pipeline installation is finalized it 1s possible to lift up the door handle ensure that the pulling hook of door handle has fastened the door locking pin successively press down the latch handle and close the pump door At this moment the surface of door handle should be in parallel with the pump If you select the drip mode or enable the drip sensor alarm function the drip sensor 16 should be installed Have the drip sensor installed between the top of Murphy s dropper
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