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Vpod Instruction Manual 

 

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When connecting this oximeter to any instrument, verify proper operation before clinical use. Refer 

to  the  instrument’s  user  manual  for  full  instructions.  The  equipment  connected  to  the  pulse 

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.   

The 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  not  come  into  contact  with  the  patient  during  defibrillation.  Otherwise  serious  injury  or  death 

could result. 

Single-use accessories should never be reused. 

Precautions   

Autoclaving,  ethylene  oxide  sterilizing,  or  immersing  the  sensors  in  liquid  may  cause  inaccurate 

readings. 

The 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.     

If liquid is accidentally spilled on the unit, clean and dry thoroughly before reuse. 

Do not try to use the SpO

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 and NIBP measurement on the same arm at the same time. This could 

potentially affect measurement accuracy. 

Notices 

Operation of this device in an electromagnetic field may influence its accuracy.   

SpO

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 measurements may be influenced by high ambient light, especially sunlight. Shield the sensor 

area if necessary. 

Dyes introduced into the bloodstream, such as methylene blue, indocyanine green, indigo carmine, 

and fluorescein, may influence the accuracy of the SpO

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 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

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 readings. 

Remove fingernail polish or artificial fingernails before applying SpO

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 sensors. Fingernail polish or 

artificial fingernails may cause inaccurate SpO

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 readings. 

Optical  cross-talk  can  occur  when  two  or  more  sensors  are  located  in  adjoining  areas.  It  can  be 

eliminated by covering each site with opaque material. Optical cross-talk may adversely affect the 

accuracy of the SpO

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 readings. 

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 equipment maintenance, please refer to the service procedures at the associated section 

as indicated in the manual. 

  As  to  the  other  concerns  for  attention,  please  carefully  look  through  the  specific  chapter  in  this 

instruction. 

 
 
 
 
 
 
 
 

1.3 Equipment symbol   

  Symbols 

Definition 

       

 

Attention

Refer  to  the 

relevant  the  prompt.  Read 

the 

operator’s 

manual 

carefully  before  using  the 

oximeter.   

 

Type BF applied part   

 

Date of Manufacture   

Содержание VPOD

Страница 1: ...s of data storage High Resolution Pulse Oximetry Records at 1 second intervals Three display modes Special design for sleep monitoring LCD Displays SpO2 SpO2 waveform Pulse Rate Low power consumption...

Страница 2: ...ights or patents and does not convey any 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 rig...

Страница 3: ...nts Basis of Operation 1 Red and Infrared ray Emitter Diode 2 Red and Infrared ray Receptor Diode 1 2 Safety Information Conception of Warning Precaution and Notice Warning Indicates a potential hazar...

Страница 4: ...ry to use the SpO2 and NIBP measurement on the same arm at the same time This could potentially affect measurement accuracy Notices Operation of this device in an electromagnetic field may influence i...

Страница 5: ...of operation Continuous operation 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...

Страница 6: ...utton 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 decrem...

Страница 7: ...as still as possible 3 2 Enter Setting mode Press the function button for about 4 second extended press the oximeter will enter into Setting mode and you will find a parameter item which include its t...

Страница 8: ...h 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 th...

Страница 9: ...gram measurement can also provide a plethysmogram wave During this mode the PR tone is dumb Fig 7 3 SpO2 plethysmogram wave PR tone modulation Beeps in sync with the patient s pulse even under most ch...

Страница 10: ...disinfecting 1 Clean or disinfect the sensor before each use 2 Unplug the sensor from the oximeter before cleaning and or disinfecting 3 Clean the external sensor surfaces and patient contact surface...

Страница 11: ...ted 2 The connection between the Probe and Oximeter is loose 1 Connect the sensor 2 Please check if the probe was connected with oximeter correctly 5 5 1 Service Method a Service hours 9 00am 5 30pm M...

Страница 12: ...he 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 Return Materials Authorization num...

Страница 13: ...Display Type OLED double color Parameters SpO2 PR SpO2 plethysmogram waveform PR bar Mode 3 display modes Record Patient ID 1 10 Data record Up to 72 hours Data transmission Transmission method Cable...

Страница 14: ...eclaration Electromagnetic Immunity for Equipment and Systems that are not Life Supporting 61000 4 6 Radiated RF IEC 61000 4 3 3V m 80Hz to 2 5 GHz d P V1 5 3 80MHz to 800MHz d P E1 5 3 800MHz to 2 5G...

Страница 15: ...minimum distance between portable and mobile RF communication equipment transmitters and the Handheld Pulse Oximeter as recommended below according to the maximum output power of the communications eq...

Страница 16: ...Vpod Instruction Manual 15...

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