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dinamap pro 200 service manualSign in Forgot Password. My Bench Close Sign In Not A Member. Sign Up Join MedWrench OK name type Receive Summary Emails. With a properly-sized BP cuff in place, just press a button to take a BP reading. It’s that easy. All DINAMAP ProCare Monitors are fully upgradeable so they can grow with your changing needs. With GE Healthcare you get more than a monitor. You get a strategic partner and a total solution. FORUMS View All (10) Ask a New Question 8 Replies -NHC Detention Facility 3 years ago 3 years ago DINAMAP GE PROCARE 200 WHERE CAN I PURCHASE PART NUMBER 107366. Reply 1 Reply -William123 3 years ago 3 years ago ProCare 200 vs Procare 200V2 What is the difference between the two units. I have a procare 200 that I am going to change the main board in but all I have is a 200v2 to replace it. I was wondering if this would cause any problems? Reply 1 Reply -Richard Shoenhair 5 years ago 5 years ago calibration blood pressure monitors By continuing to browse the site you are agreeing to our use of cookies. Please review our Privacy Policy for more details. All Rights Reserved. Trademarks Dinamap Pro 100 400 Service Manual information returns opens. Refine by: Manufacturer. Download and Read Dinamap Pro 400 V2 Service Manual manual lpw4 lister petter service manual isotemp plus refrigerator cooler fisher scientific manual tecumseh. Dinamap Pro 100 400 Service Manual from cloud storage. Bobcat T740 Compact Track. The service manual provides. GE Healthcare (9) Service Documents; Repair Center Locator; Service. Report item - opens. Besides, on our website you may read guides and another artistic eBooks online. Dinamap Pro 100 400 Service Manual. Dinamap Pro 100 400 Service Manual download. Dinamap Pro 400v2 Service Manual FREE DINAMAP PRO 400V2 SERVICE MANUAL DOWNLOAD The best ebooks about Dinamap Pro 400v2 Service Manual that you. Dinamap Pro 100 400 Service. Dinamap Pro 100 400 Service Manual PDF. General Engine Specifications.http://pls.com.ng/fckeditor/editor/filemanager/connectors/php/userfiles/brutale-1090rr-workshop-manual.xml
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Page 7 Table of Contents: Table of Contents Section 1 - Introduction 1.1 Introduction. 1-5 1.2 Addenda. 1-6 1.3 Trademarks and Trade Names. 1-6 1.4 Service Policy. 1-6 1.5 Extended Warranties. Page 8 Table of Contents: 2.6.4 BP. 2-13 2.6.5 Temperature. 2-13 2.6.6 SpO2. 2-14 Section 3- Theory of Operation 3.1 Introduction. 3-5 3.2 Overall Theory Of Operation. Page 9 Table of Contents: 4.4.1 Accessing the Clinician Mode. 4-8 4.4.2 Clinician Mode Main Menu. 4-9 4.4.3 Clinician More.Menu. 4-10 4.5 Service Mode. 4-11 4.5.1 Accessing the Service Mode. 4-11 4.5.2 Service Mode Main Menu. The model number identifies the vital signs monitoring capabilities built into the unit. Page 16 1.2. ADDENDA When this manual was published it included the most up-to-date information and procedures available. However, the specifications, design, assembly, or software controls may change. These changes are incorporated into this manual by addenda. 1.3. TRADEMARKS AND TRADE NAMES This document references terms that are proprietary, and may be registered and protected by copyrights and other applicable laws and agreements. Page 17 Introduction: Section 1. INTRODUCTION ? ? ?https://duluthtaxiservice.com/images/briggs-stratton-650-series-repair-manual.pdf A purchase order number if the product is to be sent for repairs or you order spare parts The facility's GE Medical Systems Information Technologies account number, if possible The part number for replacement assemblies or parts 1.7. SERVICE If your product requires repair service, call Customer Support and a representative will assist you. Prior to returning any product for repair, you must request a Return Authorization number. Page 18 All orders must include the following information: Facility's complete name, address, and phone number. FAX number ? Your purchase order number. Your GE Medical Systems Information Technologies account number Please allow one working day for confirmation of your order. ? 1.7.4. Replacement Accessories Replacements such as hoses, sensors, etc.Page 26 Product Description: This Page Intentionally Left Blank. Page 34 Product Description: SECTION 2. PRODUCT DESCRIPTION 2.6. SPECIFICATIONS This product conforms to the essential requirements of the Medical Device Directive. Accessories without the CE Mark are not guaranteed to meet the Essential requirements of the Medical Device Directive. IPX1 The PRO Series Monitor is protected against vertically falling drops of water and conforms to the IEC 529 standard at level of IPX1. The level of increase is approximately equal to the amount of carboxyhemoglobin present. Dyes, or any substance containing dyes, that change usual arterial pigmentation may cause erroneous readings. Page 44 Theory of Operation: This page intentionally left blank. Page 45 Theory of Operation: 3.1 INTRODUCTION 3.1 INTRODUCTION This section provides overall theory of operation and functional description of the DINAMAP PRO Monitor (hereinafter referred to as PRO Monitor). The results are then displayed on the front panel (seven segment Light Emitting Diodes (LEDs) and sent to the printer. If an over-inflation condition occurs, the OVERPRESSURE signal is routed to the PVM to release the air pressure.https://www.thelawchamber.com/wp-content/plugins/formcraft/file-upload/server/content/files/162885cff650fe---Camray-ii-boiler-manual.pdf Page 47 Theory of Operation: 3.3 FUNCTIONAL DESCRIPTION 3.3 FUNCTIONAL DESCRIPTION The following paragraphs provide the functional interface relationship. These assemblies are. Power Supply Unit (PSU) PWA. PSU Module ? Main Board ? SPO2 PWA (optional). Pneumatic control device. Liquid Crystal Display (LCD) Assembly. Page 48 Theory of Operation: 3.3 FUNCTIONAL DESCRIPTION 16 Bit ADC, Primary Processor, and Secondary Processor. The Primary Processor services and controls the Patient Parameter Interface (PPI) devices and display backlighting. The Secondary Processor controls the seven segment LED display, sound generation, real time clock, and system timing verification. The processors receive DC power from the PSU PWA. Page 49 Theory of Operation: 3.3 FUNCTIONAL DESCRIPTION communications, and isolation between SPO2 PWA and Primary Processor. Patient data received from the finger sensor is filtered, amplified, and analyzed on the SPO2 PWA. The information is sent to the Main Board via the optically coupled electrically isolated serial connection. The Primary Processor receives the data and distributes it to the appropriate display. The data is also sent to the printer via the Secondary Processor. 3.3. Page 50 Theory of Operation: 3.3 FUNCTIONAL DESCRIPTION presence. When a print command is sent to the printer from the Secondary Processor, the following will occur. CLOCK signal - transfer the data into print head. DATA IN - serial dot to be printed. LATCH signal - latch the data stream into the head. STB1-6 - cause the head to print various sections Together these signals (CONTROL DATA) cause the printer to print a graphic hardcopy of the patient vital sign values and trend data. Page 51 Theory of Operation: 3. Page 52 Theory of Operation: 3.3 FUNCTIONAL DESCRIPTION This page intentionally left blank. PRO Series 100-400 Monitor, including description of the software screens and menus used to adjust, configure and check the Monitor.BABYBASKETSONLINE.COM/userfiles/files/construction-health-safety-manual-pdf Also included are procedures to recalibrate the Monitor. Do not immerse cuffs without prior application of cuff hose caps. CAUTIONS Moisture or foreign substances introduced into the pneumatic system will cause damage to the unit. Calibration equipment should always be kept dry and clean. 4.3.2. Power Up Checks When the PRO Monitor is powered up, it conducts a series of selftests to ensure the displays and other functions are operating normally. The external power indicator LED continuously glows green to show the battery is charging. The indicator flashes every four seconds to show an external power source is connected, but is not charging the battery. Change the alarms to “Permanent Silence” mode. Set target inflation pressure This section provides an overview of the Clinician menus. The individual buttons on this menu are described briefly below. Press Button Selecting the Press button displays the target pressure dialog box, pictured above, which sets the default target inflation pressure for a BP cycle. Choosing either Yes or No will exit the menu. If silence is confirmed, the Alarm Silence button lights. More. Menu Button The More.The illustration above shows the default settings. The user can adjust the alarm limits within the ranges specified in the table below. The high limit must be at least one step higher than the low limit. Note: Predictive temperature has no alarm limit alarm. Turn the rotor to highlight a number, and push to make a selection. Enter access code 2 2 1 3. 4.5.2 Service Mode Main Menu The options accessed through the Main Service menu, pictured above, allow the technician to check basic functions of the PRO Monitor, calibrate the NIBP system, and set the language of operation. Use this menu to calibrate and check the NIBP transducers and the overpressure circuitry (Section 4.5.3). Info Button This button displays the date of the most recent NIBP calibration. Select OK to return the display to the Service menu.https://www.siscard.com/wp-content/plugins/formcraft/file-upload/server/content/files/162885e786bcca---Camry-1992-manual.pdf System Button This button accesses the System menu. In this mode, the Monitor functions as a digital manometer. The systolic LED displays the output of PT1, and the diastolic LED displays the output of PT2. With no hose attached, the systolic and diastolic displays will indicate “000.” See Section 4.7 for a more detailed description of this mode and the calibration procedure. Comms Button This button accesses the Communications menu. The settings on this menu configure communications with a host computer when PRO Monitors are connected to a network. The Remote Op check box toggles remote operation. When on, a check mark (v) appears in the box. The Monitor is tested by applying various stimuli to the sensor interfaces or by measuring of specific parameters. The test procedures employ features of the operational software and test modes of the service menus. The system will maintain the pressure for 36 seconds and will continue to display the pressure in the pneumatic system on the LCD screen. Confirm that the pressure has fallen no more than 10 mmHg while the system is pressurized. 4.6.3. NIBP Calibration Check This procedure verifies the linearity and calibration for both pressure transducers (PT1 and PT2) over the range 0-250 mmHg. If the PRO Monitor temperature system does not pass these tests, the Main PWA needs to be replaced. 4.6.7. Printer Test This test generates a sample printout from the printer. Press Accept to continue or Cancel to quit this procedure. 14. If Accept is chosen, the Monitor will vent the system to atmosphere. To ensure the integrity of these safeguards, use a safety analyzer to perform the following leakage current tests. These tests should be performed on every unit whenever the case is opened before it is returned to clinical service. If any reading exceeds the limit specified, do not return the unit to clinical service. Red Glyptol Gasket, Battery Support, Adhesive FT, RND, 12.7 DIA X 3.https://artmetinc.com/wp-content/plugins/formcraft/file-upload/server/content/files/162885d160f7e6---camry-2001-maintenance-manual.pdf5H Self-Adhesive Tape, Foam, Single Sided Adhesive, 25X. Why Use Simulators? Summary C Electromagnetic Compatibility (EMC) Electromagnetic Compatibility (EMC): ProCare Monitor Guidance and Manufacturer’s Declaration - Electromagnetic Emissions Guidance and Manufacturer’s Declaration - Electromagnetic Immunity Recommended Separation Distances Compliant Cables and Accessories All right s reserved. No part of this manual may be re produced withou t the permission of GE Medical Syste ms Information T echnologies. GUARANTEE All equi pment sold by GE Medica l Systems Inform ation Tech nologie s, is ful ly guar ant eed as to mate rials a nd workman ship for a specif ied perio d. Refer t o your warranty fo r more inform ation. GE M edic al S yste ms Informatio n T echnol ogies rese rves the right to pe rform guara ntee ser vice op eration s in its own f actor y, at a n auth orized repair st ation, or in t he custo mer ’s i nstalla tion. Our obl iga tion und er th is guara ntee is l imit ed to repairi ng, or, at o ur op tion, rep lacin g any defe ctive par ts of our equ ipment, exce pt fuses o r batt eries, witho ut charge, if such defects occur in norm al ser vice. Claims for da mage i n shipme nt sh ould be f i led promp tly wit h the tr anspor tatio n compa ny. All correspon dence cov ering th e instr ument should spec ify th e model a nd ser ial num bers. Du e t o continui ng product inn ovation, spec if ication s in thi s manual are subje ct to change wi thout n otice. Poss ession or p urchase of this de vice does no t convey a ny express or imp lied lice nse t o use t he devic e with repl acement part s which woul d, al one, or in comb inati on wi th this devi ce, fa ll with in the s cope of on e or mor e of th e pate nts relati ng to the dev ice.For the initial rel ease, al l pages ha ve the r evision le tter A. F or the se cond upda te, all pag es re ceive th e revisi on letter B.BABETRAVELLING.COM/ckfinder/userfiles2/files/compaq-presario-cq56-instruction-manual.pdf The late st lette r of t he alpha bet add ed to the tabl e belo w corres ponds to the most curren t revisio n. Manual P urpose This manual supplie s tech nical inform ation for se rvice re prese ntative s and techni cal pers onnel s o they can m aintain the equi pment t o the as sembly level. Use it as a guide for mainte nance and elect rical r epairs con sider ed fiel d repaira ble. Wh ere n ecessary the man ual iden tifies addit ional so urces of relev ant inform ation and techn ical ass istan ce. See the ope rator's m anual for th e instru ctions ne cessary to ope rate the equipm ent safe ly in a ccordance with it s func tion an d int ended use. Ordering Manuals A pap er copy of t his m anual wil l be prov ided upon requ est. Cont act y our local GE represe ntative an d reques t the part numbe r on the first page o f the manual. Safety Information The in format ion pre sented i n this s ection i s impo rtant fo r the sa fety of both the patient and ope rator. T his chapt er descr ibes ho w the te rms Dang er, War ning, Cautio n, Impo rtant, a nd Note are use d throug hout th e manual. In add ition, standar d equipm ent sym bols a re defined. R e v i s i o n Comment A Init ial Rele ase B Add E MC Complia nce T esting T ables C Upda te specif icatio ns, tests, FRU dra wings, FRU lists, forma t, and a dd erro r log feature infor mati on. D Update CE Mark Notifie d Body and equi pment s ymbols. This de vice is not int ended f or home use. Fe deral law restrict s this d evice to be sold b y or o n the or der of a physi cian. Contact GE for info rmation be fore conne cting any devices to th e equipm ent that are not recomm ended i n this man ual. Periodi cally, and whene ver the integ rity of the devi ce is in doubt, test al l functions. The u se of AC CESSORY e quipmen t not com plying with the equival ent saf ety require ments of this equip ment ma y lead to a re duced lev el of safety of the resu lting syst em. Co nside ratio n rela ting t o the c hoice shall i nclud e:.If the ins tallation of th e equipmen t, in th e USA, wi ll use 240V rather t han 120V, the sou rce must be a cen ter-tappe d, 240V, single-phas e circuit. References to Persons, Places, and Institutions Refe rences to persons, places, and inst ituti ons used within th is manual are sol ely inten ded to fa cilitate u ser com prehensi on of th e ProCare M onitor M onitor’s use and fun ction s. Extreme care h as been taken to use fict itious names a nd relat ed inform ation in th e exampl es an d illus tration s provi ded h erein. Any s imilar ity of this data to p erson s either living o r dead and to e ither cu rrent or previo usly existin g medic al ins titutions shou ld be re garde d as co incidenta l. H azard i s defin ed as a source of poten tia l injur y to a per son. DANGER in dicates a n immin ent haza rd whi ch, if not avoide d, will r esult in death or ser ious inj ury. WARNING indic ates a potent ial hazar d or unsafe prac tice which, if not avoided, could result in deat h or se rious i njury. NOTE pr ovides ap plica tion tips or other usef ul i nfor mation to assur e th at y ou ge t the most fr om your eq uipment. Product Specific Hazards Warnings. Do not use the ProCare Monit or in the presenc e of magn etic resonanc e ima ging (MR I) dev ice s. Ther e have be en re ports of sens ors cau sing pa tie nt burns when op erating in an M RI environ ment. ? Do not use the Monito r in th e presenc e of fla mmable an esthe tics. ? To help prevent unint ended current return paths with the use of high frequency (HF) su rgical equi pment, ensure tha t the H F surgical neutral electrode is proper ly conne cted. ? T o avoid pe rsonal injur y, do not perform any servicing unless qua lif ied to do so. ? W ARNIN G: These Monit ors s hould n ot be used on pat ients who are connect ed to cardiopulmon ary bypas s machines. ? If powe ring the Monito r from a n ext ernal po wer adap ter or conve rt er, use only G E Med ica l Sys te ms Informati on T echnol ogies - appr ov ed pow er adapt ers an d con vert ers. ? The Mon itor do es not includ e any user -r epl aceab le fus es. Refer servicing to qual if ied ser vice perso nnel. ? To reduce the r isk of electr ic shock, do not remove th e cover o r the b ack. Refer se rvi cing to a qual if ied ser vice perso n. ? If the accurac y of any dete rminati on read ing is questio nable, f ir st check the patient ’ s vital signs by alt ernat e means and then check the ProCa re Monitor for prop er fun ctioning. ? The u se of acce ssorie s, trans ducers and cabl es othe r than t hose sp ecified may res ult in increa sed emissi ons or decreas ed imm unity pe rformance of the e quipmen t or syste m. Caut ions ? Do not use replac ement ba tter ies oth er than the type suppl ied with th e Monit or. Replace ment batt eries are available from GE Medi cal Syst ems - Accesso rie s and Supplies. Ensure t hat the d ispl ay is func tioning proper ly before o perating the ProC are Monit or. ? Do no t immers e the Monitor in water. If th e Monito r is spla shed w ith w ater or become s wet, wi pe it i mmedia tely with a dry clo th. ? Do not gas st eril ize or aut oclave. ? Use of por table phones o r other r ad io frequency (RF) em itting equipme nt near the syst em may cause un expect ed or adverse operati on. ? The e quipmen t or sy stem should not be used ad jacen t to, o r stacke d with, other e quipmen t. If ad jac ent or s tacked us e is nec essary, the eq uipmen t or syst em sh ould be tes ted t o ver ify norm al operat ion in the conf ig uration in which it is b eing use d. ? The Pr oCar e Mon itor, when used wi th GE Me dical Syst ems In formati on Techn ologies-a pproved applie d parts and acces sories, is prote cted a gainst defi brilla tor dam age. NOTE: Th e electrom agnetic compati bil ity prof ile of the ProCare Mo nitor may change if access ories o ther th an those spec if ied for u se with the ProCare Monito r are used. Equipment Symbols The fo llowin g symbo ls are associa ted with the P roCare Monito r. Some o f the symbol s may n ot a ppear o n all eq uipment. NOTE: Th e mode l of the Monit or det ermi nes w hich sym bols ap pear on it.Europea n auth orized represe ntative. Packagin g label depi cting the tr anspor tation an d stora ge atmosph eric pressure range of 500 to 1060 hPa. WASTE OF ELECTRICAL AND ELECTRONIC EQUIPMENT (WEEE): This symbo l ind icat es tha t the wa ste of elec trical a nd electronic equip ment mu st not be disposed as un sorted muni cipal w aste an d must b e collec ted s eparat ely. Please co ntact an authorize d representa tive of t he ma nufacturer for inf ormati on concern ing the decommi ssioni ng of your equipment. Service Requirements Foll ow the se rvi ce req uire ments list ed belo w. ? Refer eq uipment ser vicin g to G E Med ical S yste ms Informat ion T ech nologie s auth orized service pers onnel only. ? Any una uthorized atte mpt to repair equ ipme nt under warranty voids that warrant y. ? It is th e use r ’ s resp onsibil it y to report the n eed for s er vice t o GE M edic al Systems Informat ion Technol ogies or to one of GE’ s autho rized agents. ? Failure o n the pa rt o f the resp onsible ind ividu al, hospi tal or institu tion us ing this equi pment to imple ment a sa tis factory ma intenan ce sch edul e may cause und ue eq uipment failure and possib le healt h hazards. ? Regu lar m ainte nan ce, irr esp ectiv e of us age, is esse nti al to en sure that the equipme nt will always be funct ional whe n requir ed. Equipment ID The fol lowing gr aphic ill ustrates the compo nents of th e monitor’s serial nu mber.The ProC are Monito r is int en ded to monit or one p atient a t a time in a cl ini cal setting. ? Federa l law ( U.S. A.) restrict s this d evice t o sal e by or on the order of a phys ician. ? To ensure pati ent saf ety, use o nly pa rts a nd access ories m anufact ured or recommend ed by G E Med ical S yste ms Informat ion T echnolog ies. Parts and accessor ies used s hall meet the requ ir ement s of IEC 60601-1-1. ? Dispos able dev ices are in te nded for single use onl y. They shou ld not be reu se d. ? Peri odica lly, and whe never the int egr ity of the moni tor is in doub t, te st all functions. Related Manuals Service Policy The wa rranty fo r this pro duct is en closed w ith the pr oduct in the shi pper carto n. All re pairs o n produ cts und er warra nty mus t be per forme d or ap proved by Product Service personn el. Una uthoriz ed re pairs wi ll void the warr anty. Onl y qualif ied ele ctron ics serv ice perso nnel sh ould re pair product s not cove red b y warranty. Service Contracts Extended warra nties can be purch ased on most p roducts. Conta ct your Sales Repre sentati ve for details and pri cing. Assistance If the produ ct fails to function pr operly, or if assistanc e, servic e or spare par ts are re quire d, con tact Custome r Suppo rt. Be fore con tact ing Cus tome r Suppor t, it is he lpful t o atte mpt to duplicat e the proble m and to check all acces sories to Manual Title 2009360-001 DINAMAP ProC are Operati on Manual Prio r to c alling, please be prepa red t o prov ide:.T o faci lita te prompt service in case s wher e the pr oduct ha s exte rnal cha ssis or case damag e, pl eas e advis e the Cu stom er Sup port repres ent ative when yo u cal l. The Cu stom er Sup port repres ent ative will r eco rd all ne ces sary i nform atio n and will p rovi de you with a Ret urn Me rchan dise A uthori zat ion Num ber (R MA). Pr ior t o return ing any product f or rep air, yo u must have a RM A numb er. Con tact GE Medical System s I nformation Te chnologie s at 1-800-558-7044. Monday th rough Friday, 8:00 a.m. to 6: 00 p.m. EST, excluding holi days. Packing In structions Follow these re commen ded pack ing instruc tions. ? Remove al l hoses, c ables, se nsors, and power cords from th e monit or before packin g. ? Pack onl y the acce ssorie s you are reque sted to retur n; place t hem in a separat e bag and in sert the bag and the product ins ide the shipping cart on. ? Use the ori ginal ship ping carto n and packi ng materia ls, if avai lable. If the orig inal shipp ing carton is not availab le. Place the product i n a plas tic bag a nd ti e or ta pe the b ag to prevent lo ose part icles o r mat erials f rom enter ing ope nings su ch as ho se por ts. ? Use a sturdy co rrugat ed cont ainer to shi p the product; tape secu rely to seal the cont ainer fo r shippi ng. ? Pack wit h 4 to 6 in.Insurance Insu ranc e is at th e cust omer 's dis creti on. The shippe r mus t initi ate claims for damage to the product. Repair Parts Repair parts can be o rdered from G E Medica l Syste ms Informat ion Technol ogie s: Via phone: 1-8 00-558-7044, or Via FAX: 1-800-421-6 841 Exchang e replac ement as sembli es such a s Circui t Board Assemb lies al so are availab le; ask the Cus tomer Support represe ntative for d etails. Please allo w one worki ng day fo r con firmat ion of yo ur order. All or ders mu st inclu de the f ollow ing in formati on. ? Faci lit y's comple te name, address, a nd phone number. F AX num ber ? Y our pu rchase order n umber. Your GE Medi cal System s Infor mation Te chnolog ies account nu mber Disposal of Product Waste As yo u use th e Pr oCar e M onito r, you w ill acc umula te so lid was tes that re qui re proper disp osal or r ecycling. These inclu de batte ries, p atient a pplied parts, a nd packa ging mate rial. Batteries CAUTION Do not incin erate batteries. The seal ed, recha rgeable b ackup bat tery cont ains lead an d can be recy cled. Th e recharge able memory b atter y is of t he Se aled Lead Acid form. D ischarge this battery prior to disp osal.