VPOD Handheld Manual Black / Silver Model
Contents
1. eH eld ec electromagnetic environment specified below The customer or the user of the Pulse Oximeter should assure that It is used in such an environment ADIENCE ectromagnetic environment reve guidance concrete ceramic tile floor converted with synthetic material the relative humidity should be at least 30 Guidance and Manutaeturers declaration Electromagnetic Immunity for Equipment and Systems that are not Life Supporting d 3s Jp 80MHz to 61000 4 6 Radiated 800MHz RF IEC 61000 4 3 2 5 d VP 800MHz to 2 5GHz 7 ve CAE m distance Fel ove fixe tran smitter d by an electroma neti m ATAK O wia ooi dech OUUIVIFA C HZ ana TE reaypney ase Sy no El ctromag ee situations IZ IS affecte ed by bsordtion and reflection people tructures objects ane oeop Ie transmitters Vpod Instruction Manual telephone Tal digs mateut c cy rec SSS TROT rail ai eect gmagnetic site D fielo ai ssh i an a r C In e andheld im er Re excee vel above the Handheld Pulse Recommended separation distances between portable and mobile RF communications equipment and the Handheld Pulse ximeter e eld Pulse intended for use in an electromagnetic environment in which radiate disturbance are controlled The customer or the user of the Handheld ulse Oximeter can help prevent electromagnetic interference maintaining a minimum distance between2. Equipment not suitable for use in the presence of a flammable anesthetic mixture air or with oxygen or nitrous oxide 1 6 Intended Use The purpose and function of the handheld pulse oximeter is to indicate measure and display the functional oxygen saturation of arterial hemoglobin SpO2 and pulse rate for adults and pediatric patients in hospital ambulatory home and S emergency medical service environments The ac oximeter is intended for spot checking these levels and not indicated for continuous monitoring t can assist the clinician diagnostically by quickly displaying the patients SoO2 and pulse rate and can additionally store 72 hours of data 1 7 Product features Compact lightweight design and simple operation Color OLED with adjustable backlight displays SpOz pulse rate and pulse bar Up to 10 patient ID and 72 hour record storage visual amp audio alarm low battery alarm Data transfer to PC for storage or printing Convenient 2 AA size alkaline batteries Suitable for adult and pediatric patient 1 8 Accessory Standard accessories RARE manual _ VPROBE V_SOFT Finger sensor compatible with The VPOD Two AA Size Alkaline batteries Subscription to Virtuox Optional accessories 1 Finger sensor for adult 2 SpO sensor for pediatric and infant 3 Software license 4 Data cable for transmission to Virtuox 5 2 year extended warranty Confirm that the items listed are packed with the pulse oxime
3. petting mode Na yon will find a parameter item which include its title and value on the top right corner of th display ref r to Fig 5 After entering the setting mode from the normal screen continually press Function button the current parameter item will be changed sequentially in the following order Br Qrightness gt ID patients ID gt Y year gt M month gt D date gt H hour gt m minute gt Second Br brightness gt PULSE OXIMETER Fig 5 Notice When setting date and time please dont insert finger b Save and exit from Setting mode Under the Setting mode press function key left key to select the desired parameter item 2 Then press Setting key right key to adjust the value Each time when you press the Setting key right key current parameter value will be added by 1 unit sequentially Double press the Setting key right key and the current parameter setting will be added by 10 units sequentially All use circular logic Press function key left key to select the next desired parameter item Then redo step to adjust the value You on n redo step to OS uhill no parameters setting need to be 4 To finish setup fleetly press both left and right keys together to confirm Then the modifications 6 Vpod Instruction Manual under the Setting mode will be saved at the same time the system will exit from Setting mode Notices
4. 1 To confirm the modification the act of pressing both buttons simultaneously must be fleet Do not press them for long time 2 When seiting date and time please don t insert finger Cancel and exit from Setting mode he modification under Setting mode will Under the Setting mode double press the Function button be cancelled and simultaneously the system will exit from Setting mode If there is no DORON under Setting mode for more than 30 seconds the system will exit from setting mode automatically CHAPTER 4 Take a measurement 4 1 Monitoring SpO2 measuring is a non invasive technique used to measure the amount of oxygenated aa and pulse rate by measuring the absorption of selected wavelengths of light The ight emitted by a red ALE EA light emitting diodes passes through the tissue and is converted into electrical signals by a photodiode After finishing the settings contained in chapter 3 plug your finger into the sensor shown as the following picture KA Se Z mn m re aon en Menm Fig 6 placement of the sensor Select the suitable sensor in terms of type and dimension a e Clip the sensor to the rational position of the patient finger And ensure that the patients nail surface is facing upward Plug sensor info SpO2 port on top panel of pulse oximeter Notice o maintain the highest degree of accuracy it is recommended that the finger and the oximeter sensor probe are kept as sti
5. 254 bpm Measurement Range 30 235 bpm Resolution pm Accuracy 2bpm or 2 the larger is applied arm Alarm Technical alarm and physiological alarm Modes Visual and audible spO2 The upper limit 100 The lower limit 60 PR The upper limit 100bpm The lower limit 60bpm Displa DOS J OLED double color Parameters Spee PR SpO2 plethysmogram waveform PR bar Mode display modes Record Patient ID 1 10 Data record Up to 72 hours Data transmission o Transmission method Cable Transmission Data Cable Interface DB9 Conr q to Pulse Oximeter USB Conr sted to PC Operation Environment Operating temperature 5C 40 C Relative humidity lt 80 no condensation Atmosphere pressure 86 kPa 106 kPa Power eu Two AA alkaline batteries Operation time About 50 hours of typical operation Transport and Storage Environment Storage Temperature 20 1 55 Relative humidity lt 93 no condensation Atmosphere pressure 50 kPa 106 kPa Classification according to IEC60601 1 Type of protection REMA powered equipment Degree of protection pe Applied Part in Mode of Operation Continuous Safety IEC Standard 60601 1 Dimensions 139mmX44mmX24mm LXWXH Weight 110g with alkaline batteries APPENDIX B 12 Vpod Instruction Manual Guidance and manufacturer s declaration electromagnetic immunity uidance and manufacture s declaration electromac netic immunit
6. The VirtuDx Total Solution No cost software me ost oximeters The industry s most cost prec ay to qu ality oxygen patients Call Toll Free 877 397 7111 e https www virtuox net Vpod Instruction Manual Copyright Our company owns all rights of this unpublished work and intends to maintain it as a confidential work We may also seek to maintain this work as an unpublished copyright This publication is to be used solely for the purpose of reference or operation of our software system No part of this work can be disseminated for other purposes In the event of inadvertent or deliberate publication we intend to enforce its right to this work under copyright laws as a published work Those having access to this work may not copy use or disclose the information in this work unless expressly authorized by our company All information contained in this publication is believed to be correct We shall not be liable for errors contained herein nor for incidental or consequential damages in connection with the furnishing performance or use of this material The information this publication refers to is protected by copyrights or patents and does not convey license under the patent rights of our company nor the rights of others We do not assume any liability arising out of any infringements of patents or other rights of third parties Contents of this manual are subject to c
7. Vpod Instruction Manual Vianutacturer s Information E rowpowermace Protected against drippin IPX1 water k 1 4 Electromagnetism interference This oximeter is designed and tested in compliance with the EMC standard complying with the internationa standard for the EMC of the electronic medical device IEC 60601 1 2 However because O non O radio frequency transmitting equi ment and other sources of electrical noise in the health care and home enyiro ments e g cellular phones mobile two way radios electrical appliances It IS Po be tnat nigh levels of Such interference due to close proximity or strength of a source may result in disruption of performance of this device This apparatus complies with the IEC_60601 1 2 international standard The requirements of this international standar are SPR 1 GROP1 and CLASS B q 1 5 Equipment classification Classification according to IEC 60601 fpr ion inst Internal electrical r r ipment According to the type of protection against Internal electrical power source equip Accordi to the degree of protection Type B equipment ASS ES R shock p yp sea According to the degree of protection Ordin ujpment enclosed equipment without agains NArmful ingress of water pro ection against ing ess of water p According to the methods of sterilization Non sterilizable Use of Liquid surface disinfectants or disinfection only According to the mode of operation Continuous operation
8. arnings ese onl SpO2 sensors provided by manufacturer Other SpO2 sensors may cause improper performance Do not use an SpO2 sensor with exposed optical components Excessive patient movement may cause inaccurate measurements e Tissue damage can be caused by incorrect operation or misusing sensor for example by 7 Vpod Instruction Manual W ing the sens n too tight Inspect the sensor site to ensure the skins integrity and the angio position of the sensor is correct More frequent inspection should be taken r n cessary Loss of pulse signal occur in any of the following situations a he sensor is too tight b USE excessive illumination from light sources such as a surgical lamp a bilirubin lamp or sunlight c A tached so cuff is inflated on the same extremity as the one to which an SpO2 sensor is 4 4 Dis The f held pulse ox oximeter T an o ia for a AS It can display the SpO gt and pulse her are three NA mo es sh AA ANA figure is pulse column display mode he second figure Is t e waveform mode he ski figure is line gure js p mode indicating SBO O2 trend PULSE OXIMETER PULSE OXIMETER 3 m 7 Three display modes PE n OX gen saturation a aS O displayed above is 98 Pulse rate va ue CEPI layed U ALE olumn Nis is use or 1 Bar es and fa ion and quality E aE oft ik motion ra noise situations rises an al s with the pulse agati dicating u al hen th ge O8 Seth ita e SpO vp ang p sp rate valu e
9. dio alarm didi didi fhe upper limit 190 pR e limit 100b The Upper m 60bpiR NOE ne the alarm is ge long press the functional button you can silence the alarm for 30 5 2 About the button 1 l Delinition of button here are in N This acts in the oximeter Power button Function button ano Setting button Power b u fon nis a As a Power On a when the unit is in an Off conditio Function unit is O a cts as a Function bu IA etting button osa a the rig ht hi of the oximeter it has no function when the power is off When p e unit is On It acts as a Setting Dutton et welinition of Button Press ere are three way S to press the button Short ress press th e button quickly the duration time should no more than 1 second Double press wo time continuous press the time between the two press actions should be no more 8 Vpod Instruction Manual Extended press Press the button for more than 1 5 seconds Long press Press the button for more than 2 seconds 5 3 Data replay and transmission The oximeter can record SpO gt and PR value for more than 72 hours but the oximeter itself has no data replay function You can transmit the history data to a PC using Virtuox software and a special t canle WA for detailed setup and operation please refer to the Virtuox website www virtuox Note Virtuox can be obtained at no charge with the purchase of this device Please contact Virtuox customer service to
10. e The installation steps are shown as Fig 2 3 Be sure to insert the batteries in the correct polarity as indicated by polarity marking and 5 Vpod Instruction Manual inside the battery compartment Fig 3 Cautions m lt gt Be sure to install batteries with correct polarities Only use the u batteries Do not use batteries not specified for this unit Do not dispose of batteries in fire If battery fluid gets on your skin or clothing rinse with plenty of clean water immediately lt Remove the batteries from this unit when you are not going to use it for a long period of time GOA one me Do not use batteries of a different type ee ee Do not use new and used batteries together Dispose of batteries in accordance with the local ordinances and regulations 2 3 Connect the sensor Connect the oximeter sensor to the top of the oximeter as shown in Fig 4 Ensure that the sensor is firmly plugged in lt gt Fig 4 Notice The connector is also applied to upload data to Virtuox software for managing data CHAPTER 3 Setup before Operation Sy a on the zp 4 i ma ort pre e Power button to power the oximeter on Notice kr maintain STA hig ce d gree fi accuracy it is recommended that the finger and the oximeter sensor probe should be kept as still as possible 3 2 Enter Setting mode ress iie function nom for about 4 second extended press he oximeter will enter into
11. e oximeter is installed or connected with such external device without our company permission as printer computer netline and lead to oximeter failure Our company will charge for the maintenance d Warranty Limitation Warranty is void If parts made from other manufacturers are used in the servicing of the device 5 5 3 User Guarantee 10 insurance disassembling refurbishing a User must read user manual carefully before operation b User must operate and perform daily maintenance under manual specifications c Power supply and environment must be maintained under manual specifications 9 5 4 Circumstances that may void the warranty The device does not remain in original condition The shell of the device is breached or cracked Evidence of water damage Accessories adulterated or appearance of physical abuse Evidence of crushing damage to the probe Original Packaging during transportation is not used Non authorized service is performed on oximeter Damage to a product as a result of not conforming to manual specifications 5 5 5 User s Special Request for Extended Warranty Our warranty is consistent with industry standards The device and accessories come standard with a 1 year warranty An extended warranty can be purchased from Virtuox at the user s request Return Policy Warranty and non warranty returns should be handled in the following manner Contact the Technical Support Department and obtain a RMA Retu
12. ed to the AE oximeter s data interface must be certified according to the respective IEC standards i e IEC950 for data processing equipment or IEC 601 1 for medical electrical equipment All combinations of equipment must be in compliance with IEC601 1 1 systems requirements he physiological data and alarm messages displayed on the equipment are for reference only and cannot be directly used for diagnostic interpretation Worn out data cables may also cause inaccurate data so if the data is used as a reference to treat a patient pay special attention to data cable and check it more frequently When using the equipment with electrosurgical units ESU make sure the patient is safe Do pe as into contact with the patient during defibrillation Otherwise serious injury or death could result e Single use accessories should never be reused Precautions n ethylene oxide sterilizing or immersing the sensors in liquid may cause inaccurate readings he operator must be thoroughly familiar with the information in this manual before using the device Unplug the sensor from the oximeter before cleaning or disinfecting it elf liquid is accidentally spilled on the unit clean and dry thoroughly before reuse Do not try to use the SpO gt and NIBP measurement on the same arm at the same time This could pO ARE affect measurement accuracy otices Operation of this device in an electromagnetic field may influence its accu
13. hanges without prior notice All rights reserved Version V1 0112 Issue Date 3rd of August 2009 Content CHAPTER 1 INTRODUCTION 2 1 1 BRIEF INTRODUCTION 2 1 2 SAFETY INFORMATION 2 1 3 EQUIPMENT SYMBOL 3 1 4 ELECTROMAGNETISM INTERFERENCE 4 1 5 EQUIPMENT CLASSIFICATION 4 1 6 INTENDED USE 4 1 7 PRODUCT FEATURES 4 1 8 ACCESSORY cccccccccecccescceesceeess 4 CHAPTER 2 BASIC OPERATION 5 2 1 OUTER VIEW eee 5 2 2 REAR PANEL 5 2 3 CONNECT THE SENSOR 6 CHAPTER 3 SETUP BEFORE OPERATION 6 3 1 POWER ON THE OXIMETER 6 3 2 ENTER SETTING MODE 6 CHAPTER 4 TAKE A MEASUREMENT 7 4 1 MONITORING o 7 4 2 MODE SWITCH uaeauua2222 7 4 3 FACTORS THAT MAY AFFECT THE MEASUREMENT 7 4 4 DISPLAY MODE 8 CHAPTER 5 OTHER INFORMATION 8 5 1 ALARM ooo eee onen nn 8 5 2 ABOUT THE BUTTON 8 5 3 DATA REPLAY AND TRANSMISSION 9 5 4 MAINTENANCE 2222 9 5 5 TROUBLESHOOTING 9 APPENDIX A SPECIFICATIONS 12 APPENDIX B e ooooooooooocooocoooococ 12 Vpod Instruction Manual Chapter 1 Introduction 1 1 Brief Introduction ae Thank E for gar the handheld
14. he batteries Ni M l fully prior to S orage lease charge over 14 hours at first time or will reduce the battery life 5 5 Troubleshooting a Error Definitions rr 1 program memory damaged Err 2 dat memory amaged Err 3 sensor Red mission ode damaged Err 4 sensor Infrared ray mission Diode damaged Err 5 sensor Infrared ra ipecele Diode damaded Err 6 exterior crystal oscillator damaged sensor emission diode or receipt diode damaged rr Err 9 real time clock damaged Em 10 EEPROM ch damaged b Possible problem and corresponding resolution Probl Possible Solution ems reason srt opO 1 Finger is no Retry Or PR plugged plugging the canno correctly inger be 2 Patients 2 Attempt displa Oxyhemoglo several time e bin value IS to obtain a norma too low to be reading If lly measured are sure that no problem exists obtain further clinical examination SpO 1 Finger might 1 Retry b or PR not be plugolng t e displa plugged inger IS deep enough 2 Urge the y unsta 2 Finger is patient to Vpod Instruction Manual ble trembling or remain still patient is moving continually The 1 Battery 1 Please Oxim power may replace eter pe batteries can inadequate 2 Please not be or not reinstall the power installed batteries edon 2 Batteries 3 Contact
15. ll as possible 4 2 Mode switch After turning on the oximeter each time the function button is pressed the oximeter will switch to another display mode shown as Fig 7 4 3 Factors that may affect the measurement During operation the accuracy of oximeter readings can be affected by the following factors 4 3 1 Instrument performance depends on the pulsatile character of the artery The measurement would not be considered reliable and accurate if the following conditions are present during measurement l Shock or cardi c arrest e digit e emp rature ol th z Alter the administration of a cardiovascular drug mia Evidence of ventilation perfusion mismatch 4 3 2 Instrument performance Beene on the wavelength absorption for oxyhemoglobin and deoxyhemo lobin _ f there are substances absorbing the same wavelength this would ind ce false or low Sp z values The following may affect these values car Oxy emoglobin emethe oglopin ne blue singinyle IgO carmin 4 3 3 my high illumination could affect the SpO measurement Use a semi translucent or opaque cover to shield the sensor 4 3 4 Oth r factors a o pjgntrequency electrosurgical interference from external devices including defibrillators men RCA T opan extremity that currently has installed a blood pressure cuff arterial he patient nas hypotension severe vasoconstriction severe anemia or hypothermia An arterial occlusion proximal to the sensor A W
16. local might be customer installed Technical neal Service e Oximeter might REESE KE damaged Error Receiving 1 Contact local sh SHE may be customer Error ZA Or Technical aged Service Displa alei with 2 Contact local ye broken customer on connector Technical scree 2 Mechanical Service n Misplace for 3 Contact local receive emis customer sion diode Technical 3 Amp circuit Service r malfunction Be Error 1 Emission 1 Contact local diode customer displa damaged Technical yed 2 Current Service on control circuit 2 Contact local scree malfunction customer n Technical Prop 1 The sensor 1 Connect the e off isnot sensor displa connected 2 Please yed 2 The check if the on connection probe was scree between the connected with n Probe and oximeter Oximeter is correctly loose 5 5 1 Service Method a Service hours 9 00am 5 30pm Monday Friday b Service support Telephone and e mail support Parts Replacement Virtuox will replace parts if necessary free of charge during the warranty period 5 5 2 Exemptions and limitations a Not responsible for damage caused by force majeure For example fire lightning flood cyclone hail and earthquake b Warranty expiration The corresponding cost of repackaging and shipping the oximeter or its components c Damage caused by a third party d Damage and caused by user or its representative not in compliance with the operator s manual e Th
17. nsafe practice that if not avoided will result in death or serious injury gt Precaution Reminds the user to pay close attention to device operation failure of which may cause abnormal function of the instrument gt Notice Informs the user of other important information by suggestion requirement and supplement Warnings e Please read this manual carefully before using this device The user must check that the equipment functions safely and ensure that it is in proper working condition before being used o avoid explosion hazard do not use the oximeter in the presence of flammable anesthetics vapors or liquids Do not open the equipment housings electric shock hazard may exist All servicing and future upgrades must be carried out by the personnel tralned and authorized by our company only Do not use the pulse oximeter in an MRI or CT environment he pulse oximeter is specified for use by medical professionals only e Prolonged use of the probe sensor or the patients condition may require changing the sensor site periodically Change the sensor site and check skin integrity circulatory status and correct ULA at least every 4 hours Prolonged use may cause blisters skin deterioration and iscomfort o 2 Vpod Instruction Manual eVVhen connecting this oximeter to any instrument verify proper operation before clinical use Refer to the instruments user manual for full instructions The equipment connect
18. portable and mobile RF communication equipment transmitters and the Handheld Pulse ximeter as recommended below according to the maximum output power of the communications equipment eparation distance Rated according to frequency of maxim transmitter m um output 150KHz Power to transmi MHz tter W d 3s P UT 0 3083 0 9093 U LO 40 36893 36898 77386 100 11788 11 6867 23 3334 ou ar listed E T A SR ask s ne j f Awa S ACC IN A EL A i ada sa A m HOME anc Wig M 7 ctromauneltc al ection from S led B Ores O mee Deop Te Vpod Instruction Manual 15
19. pulse oximeter The device is designed to measure SpO gt and AJ delivering visual and audio alarm sensor off alarm Please read this manual carefully before using it ee The illustrations used in this manual may differ slightly from the appearance of the actual roduct easurement principle The principle of pulse men is based on the red and infrared IR light absorption of oxygenated and deoxygenated hemoglobin present in the circulating blood Oxygenated hemoglobin absorbs more IR and allows more red light to pass through Deoxygenated hemoglobin conversely absorbs more red light and allows IR light to pass through The detector probe is placed on the finger he p contains two light emitting diodes LED s one in the visible red spectrum The beams of light rom this probe pass through the tissues and some light is absorbed by the blood and soft tissues depending on hemoglobin concentration The amount of light absorption at each light frequency is dependent on the degree of oxygenation of hemoglobin within the tissues The microprocessor can select out the absorbance of the pulsatile fraction of blood i e that due to arterial blood from constant absorbance due to non pulsatile venous or capillary blood and other tissue pigmenis YVYV i R d ay z icy Emitter Diode Re 2 Red and Infrared ray Receptor Diode 1 2 Safety Information Conception of Warning Precaution and Notice gt Warning Indicates a potential hazard or u
20. racy SpO measurements may be influenced by high ambient light especially sunlight Shield the sensor area if necessary e Dyes introduced into the bloodstream such as methylene blue indocyanine green indigo carmine and fluorescein may influence the accuracy of the SpOz reading Any condition that restricts blood flow such as use of a blood pressure cuff or extremes in systemic vascular resistance may cause a failure to determine accurate pulse rate and SpO gt readings Remove fingernail polish or artificial fingernails before applying SpO gt sensors Fingernail polish or artificial fingernails may cause inaccurate SpOs readings eOpiical cross talk can occur when two or more sensors are located in JOL areas It can be eliminated by covering each site with opaque material Optical cross talk may adversely affect the accuracy of fhe SpOz readings e Obstructions or dirt on the sensor s red light or detector may cause a sensor failure Make sure there are no obstructions and the sensor is clean For routine n maintenance please refer to the service procedures at the associated section as indicated in the manual o ani other concerns for attention please carefully look through the specific chapter in this instruction 1 3 Equipment symbol Symbols elmion A Attention Refer to e relevant the prompt Read the operators manual carefully before using the oximeter ype BF applied par Date of Manufacture
21. rn Materials Authorization number The RMA number must appear on the outside of the shipping container Return shipments will not be accepted if the RMA number is not clearly visible Please provide the model number serial number SN and a brief description of the reason for return Freight policy 1 Within Warranty The customer is responsible for freight A insurance charges when the equipment is shipped to Virtuox for service Virtuox is responsible for the freight A insurance charges from us to the customer 2 After Warranty The customer is responsible for any freight 8 insurance charges for returned product 5 5 6 Repackaging for returns e Place all accessories in a watertight Ziploc bag e Use original package and packing material if possible User will be responsible for damage caused by improper packaging during transportation Ensure the RMA number is clearly printed on the Box e Include an insert describing the reason for the return Vpod Instruction Manual APPENDIX A Specifications Notices S duej a may be Cangen without prior notice e The circuit diagrams the list of components the illustration of diagrams and the detailed rules of calibration are provided exclusively to professional personnel authorized by our company Spo Display Range 0 100 Measurement Range 70 100 Resolution Yo Accuracy 80 100 2 10 9 3 m 0 69 unspecified Heart Pulse Rate Display Range 0
22. s may e SU Seni M ia ram e ed to de uP inet 9 da S tu BEKO of sree A id he artendl blood M tc for example 98 emagiobin g molecules int e re Ge Is of T art rial blood m nes with oxygen then he blood Has as THESES saturat as of numeric on t bi Oximeter will read poe rer to Lg om Os numeric shows ine per enta BL h mog in m TE which have combined with oxygen molecules to form okyh Smoglo he SPO 2 piel nysmegram BG Sp SEO UE smogram wave During t is mode t 6 PR tone is d m tone nfo du Lt ash Beeps in sync with the patients pulse even under most challenging bala e mor conditions CHAPTER 5 Other information 5 1 Alarm Alarm Technical alarm and physiological alarm Technical alarm finger out probe off power low and error code In the situation that the finger is nop inserted gorrggti ly or tne connection state of the probe is not good results in failure of measurement Finger out or Sensor off may be displayed on the normal screen When battery power is lower than 2 7 0 1V the sign m will flicker in its display area Replace the batteries as soon as possible In the failure state the oximeter will dis error codes and will automatically power off if the error A ais jay la sts for more than 8 NE For the details and eno On Error please refer to hysiolo a aarm SpO and PR th eme sured p and qr PR value is beyond nd the Gefaylt limit alarm will be activated and the seu ing value will flash with au
23. set up an account 87 7 33 111 5 4 Maintenance lt is very important Ior uer 19 perform daily maintenance of oximeter and parts in order to maintain its Disi function and appear nfection procedures may be performed with the use of the below mentioned cleaner disinfectants F i to form thege procedures may result in invalidating the W ilur er Loca SU prot cols wil pp Please fake out battery before cleanin ing ximeter he external surface of the oximeter e cleaned by wiping with a damp cloth Do not submerge he oximeter in any solution at any time To do so will void the Warranty segne Ao owin ar solutions e lutaraldehyde A 10 Bleach solution Ma soapy the following Cleaner O Do not usgth S O Any kind scrubbing or scouring solution o Ac tone o Alcohol based cleaners Probe cleaning and disinfectin J Crean opdisintect the sense ISI r before each use Unplug the sensor from the AUDE cleaning and or disini cting 2 3 gan he external sensor surfaces and patient contact surfaces with a Soft cloth moistened wit water or a mild detergent solution a gt 4 osa m sensor wipe the surfaces with a disinfecting solution Isopropyl alcohol is 2 Do not immerse the sensor in any solution To do so will void the warranty Batfar Do not sterilize the sensor by irradiation steam autoclaving or ethylene oxide maintenance l l V tteries MAW not be using the oximeter for a long time Sarge t
24. ter If any item on this list is missing or damaged contact your distributor Contact the carrier immediately if the shipping carton is damaged Vpod Instruction Manual CHAPTER 2 BASIC OPERATION 2 1 Outer View Fig 1 Description of Fig 1 1 Double functional socket for oximeter probe and data transfer cable Oximeter probe socket Connect the probe with the oximeter before taking a measurement Data cable socket Connect the oximeter with PC by a data cable for transferring data recorded to Virtuox software 2 The function button short press the button to change the display mode on the measurement Se eet ae the normal screen extended press the button for about 4 seconds to change the setting items 3 The POWER on off button Note If no press on any button for 30 seconds the oximiter will power off automatically 4 The Setting button Press this button repeatedly to increase the parameter under adjustment by one decrement 5 Display screen displays date and time SpO2 data PR data error information etc 2 2 Rear Panel Battery wharf cover Fig 2 Install the batteries The oximeter can be powered by 2 AA Size alkaline batteries which will typically provide 50 hours of continuous operation or by the optional rechargeable battery pack When battery power is lower than 2 7 0 1V the sign H will flicker in its display area Replace the battery or rechargeable batteries as soon as possibl
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