IVAC’ P1000, P2000 & P3000 DIRECTIONS FoR UsE - GB PURGE/BOLUS ~ Use to complete syringe VOL INFUSED (P1000 only) - Press to dieplay the volume of fluid priming when tho unit 1s stopped prior to _ infused. Connecting the extension set to the patient and to CONFIRM SYRINGE SIZE (P2000 / P3000) - Press to confirm the deliver a bolus infusion at purge rate, size ofthe syringe flashing in the syringe size dispiay. SET ALARM LEVEL (P3000) - Press and hold down, START Bullon - Press to start the then use the down arrow to select the pumping infusion pressure alarm level jaa ‘STOP Button - Press to stop the infusion and silence any ae ‘alarms. The Amber a { er. | eeu 60.0, Geta Z j { * ] 1 AG POWER - Whan tluminatod to VOLUME GLEAR (P1000 cry - th ho unt stopped press Uni enna o AC poor an incanneten win vue nan Vue adores VOLUME ¢LEAR (P2000%2000) - Wh the unt stopped BATTERY - When Huminatd the pump ra a racine Rear Ce press for 1 second to reset the volume infused to zero. Press. in conjunction with Volume Limit to reset the value to zero. RATE - Pres the chevrons to increase and desreass the infusion VOL LMFT - Use the chavrons to set a volume iit. When pump rate when the pump is in STOP. Use in conjurt with Volume jg stopped press the Volume Clear to a displayed value to Limit sot the volume tit. zero. Press to display the sloredvolum IntOdUCtOM. oes cesvisessesnesusveee "pe Paes cr cs p16ss bunso G Pasee IVAC® “P* Series Syringe Pumps are designed for the accurate Frat Pra ata Dt ‘administration of continous infusion, Comprohensive alarms and sophisticated monitoring systems combine with simple operation fo make these instruments. suitable for general and critical infusions. [eek ceed 7 ¢ Volume Infused Display on P2000 & P3000 Sais etl lcape eames ones 7 © =~ Purge and Bolus Infusion Capability Fite ia ia lilt =tllemaeeinapacaie sige gee raed Gant Syringe Sie PE000 & P00 Only. 07-1 loternal Battery fr portable uae ‘Set Pressure Level - P3000 Only . 7 ° Unique IVAC® Pumping Pressure Monitoring System ‘General Options 7 . ei 6 ° Optional communications and nurse call interfaces ‘Self Test Routine. ¢ Volume Limit Facility oe neta 4 entre ‘Specifications i 9-10 ee : 7 Denies pea pees ‘Maintonance Procedures... ..-.+ t Main Display ae ened : Bera card i Beseter etcetera 7 7 oe ' 2 Volume Infused Display Pumping Pressure Display i “ T114Tea0rsatit? iaave 20Cea [S| Luer-Lock / This IVAC® pump has boon calibrated for use with single use disposablo syringes. To ensure correct and accurate operation, only use Luer-Lock versions of the syringe make specified on the pump or described in the directions for use. Use of non- specified administration sets or syringes may Impair the operation of the pump and the accuracy of the infusion. Uncontrotied flow or syphoning may result ifthe syringe is located on the pump without its finger grips and plunger correctly located in the slots provided, or if it fs removed from the pump before the extension line Is properly Isolated from the patient. Isolation may include closing a tap in the patient lin or activating a flow stop clamp. ‘When combining soveral apparatus andior instruments with administration sets and ‘other tubing, for example via a 2 way tap, the performance of the pump may be Impacted and should be monitored closely. Do not mount the pump in a vertical position with the AC power inlet or the syringe pointing upwards as this could affect electrical safety, in the event of a fluid spill over the unit or lead fo an infusion of air which may be in the syringe. To protect against {the Introduction of air the user should regularly monitor the progress of the Infusion, ‘syringe, extension line and patient connections and follow the priming procedure specified herein. This is a positive pressuro device designed to achiove very accurate fluid administration by automatically compensating for resistance encountered in the infusion system. The pumping pressure alarm system 1s not designed to provide protection against, Cr detection of, infitration conditions which can occur at low pressures. ‘Several alarm conditions detected by this pump will stop the infusion and generate audible alarms. Usors must porform regular checks to ensure that the infusion is progressing correctly and no alarms are operating. This instrument is protected against the offects of oxtornal interference, including high energy radio frequency omissions, magnetic fields and electrostatic discharge (for example, as gonerated by electrosurgical and cautorising equipment, large motors, portable radios, cellular telephones etc.) and is designed to fall safe if unreasonable levels of interference are encountered. In some circumstances the unit may be affected by an electrostatic discharge of +/- ‘kV (contact), +/-16KV (ain), at test levels fower than these values the unit will operate normally. In rare circumstances the unit may be affected by radiation at a level of 10V/m. If the unit is affected by this external interference the unit will fail safe or reset, (a call back alarm will occur after 2 minutes). Should false alarm conditions be encountered either, remove the source of the interference, or regulate the infusion by another appropriate moans. This unit emits a certain level of electromagnetic radiation which is within the levels specified by 1EC60601-2-24 and IEC60601-1. If however tho unit interacts with other equipment, measures should be taken to minimise the effects, for instance by repositioning or relocation. IT this instrument is dropped, subjected fo excessive moisture, humidity or high tomperature, or otherwise suspected to have been damaged, remove it from service for inspection by a qualified service engineer. An explosion hazard oxists if the instrument Is used in the presence of flammable anaesthetics. Exercise care to locate the unit away from any such hazardous sources. ‘An electrical shock hazard exists if the units casing is opened or removed. Refer all servicing to qualified service personnel. A comprehensive service manual containing circuit descriptions, servicing and testing information is available for this unit. It can be ordered from your ALARIS Medical Systoms® authorised distributor (Technical Service Manual Part Number +1000P800048) Dia Wacrsorta sue 0awa) ‘Check that the pump is complete, undamaged and that the SEE ea ae et etoea Seon tant soeasdom as nes ‘Systems® syringe pump are; IVAC® P SERIES PUMP POLE CLAMP DIRECTIONS FOR USE ‘AC POWER CABLE (AS REQUESTED) PROTECTIVE PACKAGING Connect the unit fo the AC power supply for 24 hours to ensure that the internal battary is fully charged. ‘Shouid the pump fall to perform correctly, replace it in its original protective packaging and contact a qualified service engineer for investigation. provide secure fixing to standard |.V. poles of a diameter of up to ir ‘The pole clamp can also be fitted in a choice of 4 fixing positions allowing the unit to be mounted to vertical and horizontal poles, ‘equipment rails and hospital furniture in a variety of conveniont operating orientations. ‘Tho pole clamp may be adjusted for use with horizontal fitings by Using the existing fixing screws with the alternative fixing holes in ‘the pole clamp. ‘The pole clamp may be also secured to the base of the unit in a choice of four positions. Important: Do not mount the unit with the AC power inlet or the syringe pointing upwards. This could affect the electrical safety in the event of a fluid spill or load to the infusion of air which may be in the syringe. co THE MAINS FUSE Ifthe pump continualyfluminates the battery symbol and the AC ower indicator light does not illuminate when the pump is Connected o the AC power supply and switched ON, suspect thet either, the power supply fuse in the AC power plug, or, the intamat fuse has blown, First check the power supply fuse in the AC mains plug, ifthe AC power indicator light does not illuminate remave the pump from service. Its recommended that the mains fuse is only replaced by 8 qualified service engineer. Far further information regarding the replacement ofthe Internal fuse refer to the technical servies ‘manual. Place the pump on a stable horizontal surface or secure using the ae Prepare, load and prime the single use disposable syringe and esl nepal Important: Only use a syringe of the type stated on the pump tebolting. ‘1. Squeeze the finger grips on the plunger holder and side the ‘mechanism to the left. Lift the syringe clamp and rotate to the let. 2. Insert the syringe into the slots on the plunger holder. ‘Squceze the finger grips on the plunger holder and slide the mechaniam to the right uni the syringe finger flanges locate inthe V sit Important: Advance the syringe until the finger flanges touch the front of the V slot closest to the syringe clamp. This is Important to prevent delay at the start of the infusion. 4. Rotate the syringe clamp forward until it locks onto the syringe barrel 5. Check that the syringe plunger and finger flanges are correctly located in thelr slots, Important: Only use a syringe of the type and size indicated ‘on the pump or in this manual. Using an incorrect syringe could adversely affect the accuracy of the infusion and the performance of the pump. When initially loading the syringe, allow for the volume of fluid contained in the extension line and retained in the syringe at the end of infusion as this ‘dead-space’ wil not bo Infused. | %e 7 = %, sn) ‘Obsrvaton mine) ‘amin Flow Rate Smt rampet Cave ater) 7. = ‘raeenin) Certon nx oes) ‘ype Flow rte and Trumpet cores abovs, using BD Platina Som synge wth admnistton eet 30402. ‘Trapt curve vies shou minimis mum peronnag ral evr a2 rifle an ong Wm Mee accuracy Spee Seed z = = Rhos Cent ett caer ees iene Rae eene as ; a sh Benet ee Eo. eee E af... choatme eae cent rt Peiomarc wets: 20 8 Cwtomates wn ogee 1 NAG, Zee, Sebrarmasthaee 08 cue 8 eet Et tere eccentric ty ee eee eran (co Se eee meereatee eee Seah Usenet valton over the range -10bnwHg, agua fo wer height 4-1, wl proce trumpet curves withthe Hie shown above W214 _to00PH0TT2 sce boLe el “The following details outline the safety checks designed into IVAC® Syringe Pumps to minimise the possibilty of under/over infusions. MONITORING OF THE SYSTEM CLOCK FREQUENCY / WATCHDOG “The systam clock , which is used to control the rate of the pump is derived from the microprocessor crystal oscillator. A watchdog circuit {s implemonted in the pump to monitor the correct time period. The watchdog circuit requires tha microprocessor to sond a reset pulse ‘every 10mS to stop the counter from timing out and triggering the watchdog alarm. The reset signal has to be in a time ' window’ of botwoon 8 to 12mS. If itis ether too fast or too slow the watchdog hardware will detect this and generate an alarm and disable the ‘motor drive. Additionally, on power up the watchdog is allowed to time-out and the period is measured and tested to be within a set {olerance. This then confirms that both the microprocessor crystal and the watchdog crystal frequencies ara correct. DETECTION OF LINEAR MOVEMENT Linear grid with optical switch is incorporated in the unit to detect the movement of the pumping mechanism. This movement is ‘moritored in the electronics and software of the system. If itis detected that the mechanism Is elther moving too fast, 100 slow, or not ‘moving at al then an error code will be Gisplayed, the motor drive will be disabled and the pump will stop. CONTROL OF LINEAR SPEED / INFUSION RATE The pump mechanism Is driven using a d.c. motor; feedback for tho control system is provided by two opto switches. To enable the ‘motor dive there are three transistors which need io be turned on. The correct operation ofthese ransistors is tested on power up. The control system monitor the feedback from the opto encoders and adjusis tho motor on time to maintain the requlred speed. if there are no encoder signals feedback, indicating thet an opto has failed or the transmission has jammed, an error code willbe displayed and the pump wil fiksafe. If there are too many encoders detected an error code willbe displayed and the pump wil fai-safe. The pump calculates the eppropriate motor contol rate from the eet infusfon reto and syringo constant cata stored within the pump software. The syringe constant data converts m's to mm's of movement for each syrings type and size, SPARES AND SERVICE EQuiPMENT ‘A comprehensive list of spare parts for IVAC® Syringe pumps is These IVAC®“P" Series Syringe pumps have been designed to included within the service manual. This can be ordered from allow simple and low cost servicing. Standard components are ALARIS Medical Systems®, or authorised distributor. For part _ employed where possible so that no special test, calibration or ‘number please refer to summary parts list below: tools are requited. However, the following items may be useful for Part Number Description ence : 4000PBO1112 Directions For Use IVAC® Pioga/2000;g000 ‘Part Number Descriotion (00007600020 celusion Test Gear 1000PB00048 Technical Service Manual IVAC® “P* Serios Syringe Pumps ‘0000TG00080 Linear Accuracy Test Gear ‘0000E1.00004 intemal Battery - 6VNP2.8-6 Rechargeable T000EL00043 Ribbon Cable Extension 1O01FAOPTS1 AC Power Lead - U.K. poneecnee i oreaa appar 4001FAOPT2 AC Power Load - European 00005600010 50m) Syringe Sizing Test Gear japiPApE TEST AG Baie Lead linia (0000600011 100ml Syringe Sizing Test Gear 1000SP00078 Pole Clamp Assembly 10001801009 Label Set V4 T3114 1000PBOT ave 50uncon ALARIS Medical Systems® (hereinafter referred to as “ALARIS") ‘warrants thet! (A) Each new instrument (pump, controller or peripheral Instrument) is free from dofects in material and workmanship under normal use and service for a period of one year from the dato of delivery by ALARIS to the first purchaser. (®) Eech new accessory is free from defects in material and workmanship under normal use and service for a pariod of rinety (80) days from the date of delivery by ALARIS to the fist purchaser. I any product requites service during the applicable warranty period, the purchaser should communicate directly with the local ALARIS service centre to determine appropriate repair facility. Repait or replacement will be carried out at ALARIS's expense, ‘subject to the terms ofthis warranty. The product requiring service should be retumed promptly, properly packed, and postage propaid. Loes or damage in return shipment to ALARIS shal! be at purchasers risk. In no ovent shall ALARIS be liable for any incidental, indirect or ‘consequential damages in connection with the purchase or use of ‘any ALARIS product. This warranty shall not apply to, and ALARIS shall not be responsible for, any loss arising in connection with the purchase or use of any ALARIS product which has beon repaired by anyone other than an authorised ALARIS service representative or altered in any way so as, in ALARIS's judgement, to affect its stability or reliabilty, or which has been ‘subjact to misuse or negligence or accident, or which has had the ‘serial or lot number altered, effaced or removed, or which has been used otherwise than in accordance with the instructions furnished by ALARIS. ‘This warranty isin lieu of all other warranties, express or implied, and of all other obligations of liabilities on ALARIS's pari, and ALARIS neither assumes nor authorises any representative or ‘other person fo assume for it any other liability in connection with the sale of ALARIS products. See packing inserts for international warrenty. ALARIS DISCLAIMS ALL OTHER WARRANTIES, EXPRESS OR IMPLIED, INCLUDING ANY WARRANTY OF MERCHANTABILITY OR FOR FUNCTION OF FITNESS FOR A PARTICULAR PURPOSE OR APPLICATION Peck) For service contact your local ALARIS Medical Systems® Afiate Office or Distributor, ALARIS Madical Systems® Service Centre Addresses: AE HU ALARIS Medical Systems Middle ALARIS Medical Systems Office East Office, Débrentel ter 1, PO Box 5527, H- 1013 Budapest. Dubai, United Arab Emirates. Magyerorszég. Tek: (971) 4 26 22 842 Tek: (36) 12 14.2220 Fax: (@71)4 2822014 Fax: (36) 1201 6887 au T ALARIS Madical Austraia Pty Ltd, ALARIS Medica! ttalia SPA. ‘31167 Prospect Highway, Via Ticino 4, ‘Seven Hille, NSW 2147, 50019 Sesto Florentino, Australia. Fironzo, Italia. Tet (61) 2.9888 0255 ‘To: " (20) 055 34 00 22 Fax: (61) 29674 444g Fax. (88) 086 94 00 25 NL ALARIS Medical Holland, BV. Kantorenpand "Hoefse Wing”, Printerweg 5, 3821 AP Amersfoort Tel: (82)2 263.0975 Nederiand Fax (82) 22679021 Te: (31) 33.455 51 00 CA Fax (31) 3348551 01 ALARIS Medical Canada, Ltd, NO. 8976 Whitle Read, ALAR'S Medical Norway A'S Suite #120, Hamang Terrasse 56, Mississauga, Ontario L4Z3N1, PO Box 248, Canada, N-1901 Sandvika, Norge. Tok (1) 906-507-1191 Tel: (47) 6757 68 60 Fax: (1) 805-507-6664 Fax: (47) 6757 58.60 nN NZ ALARIS Medical NZ Lid, Unit 14, 13 Highbrook Drive, Ezst Tamaki, Auction, ALARIS Modical Systems Office, ‘Suite 401 No, 88 Chang Su Road, ‘Shanghal PC 200040, oe anew or cayeecesameset tfc see saa Regus Sime te se LARS Val Dosen, ALAR Madea Nede, AB aes ana Se 2 BS eatne Beta oe eee SI as aces sozco Deter vores =e SSL a zee, | oe ALAR Nae youn Otes, es Se ea ALARIS Medical E: SL. #40-D4 OCBC Centro, verde Valdepaa 2 Singapore 080515, oS re 28108 - Alcobendas, Madrid, Fox (85) 5345516 covmran Siac ALAR Medal ene or eee 10221 Wateridge Circle fe ean foie er one Acne Medea, SA, FL (NO MEA ES 7810 St Germain on Laye Cedex, ZA Franco. 4 TE cay10 spoorm Mawel Pa Pret) ae ea ‘Oude Molen Road, Ndebeni, Cape GB - Manufacturer's Ackiress: Town 7405, South Africa, ALARIS Medical UK Lid., Tel: (27) 0860 597 572 ‘The Cresoont, ys Close, Fac (7)216107667 Basingstoke, Hampshire, G22 488, United Kingdom. Tok (44) 0800 980 6972 Fax (44) 1256388411 Tata TDOOPBDTTTD eave 30