SurgivetÂ® V1030 Hand-Held Pulse Oximeter

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Chapter 1: Introduction WARNING! Measurements made at sites with low perfusion are potentially inaccurate. Always use measurements in conjunction with other clinical signs and symptoms. WARNING! SpO 2 measurements may be adversely affected in the presence of high ambient light. Shield the sensor area (with a surgical towel, for example) if necessary. WARNING! Dyes introduced into the bloodstream, such as methylene blue, indocyanine green, indigo carmine, fluorescein, and patent blue V (PBV) may adversely affect the accuracy of the SpO 2 reading. WARNING! Any condition that restricts blood flow, such as use of a blood pressure cuff or extremes in systemic vascular resistance, may cause an inability to determine accurate pulse rate and SpO 2 readings. WARNING! Optical cross-talk can occur when two or more sensors are placed in close proximity. It can be eliminated by covering each site with an opaque material. WARNING! Significant levels of dysfunctional hemoglobins, such as carboxyhemoglobin (with CO-poisoning) or methemoglobin (with sulfonamide therapy), will affect the accuracy of the SpO 2 measurement. WARNING! Tissue damage may result from overexposure to sensor light during photodynamic therapy with agents such as verteporphin, porfimer sodium, and metatetrahydroxyphenylchlorin (mTHPC). Change the sensor site at least every hour and observe for signs of tissue damage. More frequent sensor site changes/inspections may be indicated depending upon the photodynamic agent used, agent dose, skin condition, total exposure time or other factors. Use multiple sensor sites. WARNING! When connecting this monitor to any instrument, verify proper operation before clinical use. Refer to the instrument’s user manual for full instructions. Accessory equipment connected to the monitor’s data interface must be certified according to the respective IEC standards, i.e., IEC 60950 for data processing equipment or IEC 60601-1 for electromedical equipment. All combinations of equipment must be in compliance with IEC 60601-1-1 systems requirements. Anyone connecting additional equipment to the signal input port or the signal output port configures a medical system, and therefore is responsible that the system complies with the requirements of the system standard IEC 60601-1-1. WARNING! This monitor is suitable for use within the patient environment. IEC 60950 approved equipment must be placed outside of the patient environment. The patient environment is defined as any volume in which intentional or unintentional contact can occur between the patient and parts of the system or between the patient and other persons touching parts of the system. 1-4 Veterinary V1030 Hand-Held Pulse Oximeter Operation Manual
Chapter 1: Introduction Figure 1.1: Patient Environment (side). The dimensions are not prescriptive. Figure 1.2: Patient Environment (top). The dimensions are not prescriptive. WARNING! The oximeter will not operate without batteries installed. Properly charged batteries provide a reserve source of power in case of external power failure. Never use an oximeter with discharged batteries to monitor a patient. WARNING! Inspect battery terminals for corrosion or contamination. The monitor may not operate properly or could fail to alarm if battery terminals are corroded or contaminated. Do not use until battery terminals have been properly cleaned and repaired. WARNING! Check expiration date of batteries. The monitor may not operate properly or could fail to alarm if expired batteries are used. Do not use until proper batteries can be obtained. WARNING! Remove device batteries prior to long term storage. WARNING! Disconnect the external power supply from the monitor or Docking Station before disinfecting or cleaning the monitor. WARNING! Do not plug the monitor or Docking Station into an outlet controlled by a wall switch. WARNING! Disconnect the AC power supply from the outlet before disconnecting it from the monitor. Leaving the AC power supply connected to an AC power outlet without being connected to the monitor may result in a safety hazard. Veterinary V1030 Hand-Held Pulse Oximeter Operation Manual 1-5
Page 1: Surgivet® V1030 Hand-Held Pulse Ox
Page 4 and 5: Table of Contents Pulse Oximeter Se
Page 6 and 7: Table of Contents Pulse Rate.......
Page 8 and 9: Warranty and Service Information Li
Page 10 and 11: Chapter 1: Introduction SYMBOL DEFI
Page 14 and 15: Chapter 1: Introduction WARNING! Do
Page 16 and 17: Chapter 1: Introduction Notes NOTE:
Page 18 and 19: Chapter 2: Intended Use and Monitor
Page 20 and 21: Chapter 3: Controls and Features Ch
Page 22 and 23: Monitor Operating Keys Chapter 3: C
Page 24 and 25: Chapter 4: Operating Instructions C
Page 26 and 27: Installing the Batteries Chapter 4:
Page 28 and 29: AC Power Plug the AC power supply i
Page 30 and 31: Chapter 4: Operating Instructions A
Page 32 and 33: Chapter 4: Operating Instructions F
Page 34 and 35: Chapter 4: Operating Instructions W
Page 36 and 37: Chapter 5: Changing the Monitor’s
Page 42 and 43: Factory Defaults Chapter 5: Changin
Page 44 and 45: Chapter 6: Alarms High Priority Ala
Page 46 and 47: Chapter 6: Alarms TYPE DISPLAY INDI
Page 48 and 49: Chapter 6: Alarms saving changes, w
Page 50 and 51: Chapter 8: Optional Docking Station
Page 52 and 53: WW1090 Lithium-Ion (Li+) Rechargeab
Page 54 and 55: Attaching the Printer Chapter 8: Op
Page 56 and 57: Choosing the Print Mode Chapter 8:
Page 58 and 59: Chapter 9: PC Communication Setup C
Page 60 and 61: Output Format Chapter 9: PC Communi
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Chapter 10: Maintenance CAUTION! Di
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Chapter 11: Troubleshooting Power P
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Chapter 11: Troubleshooting PROBLEM
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Chapter 11: Troubleshooting This pa
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Chapter 12: Optional Supplies and A
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Chapter 13: Specifications SpO 2 Sp
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Chapter 13: Specifications Power Re
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Chapter 13: Specifications This pag
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Appendix A: Guidance and Manufactur
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Appendix B: SpO 2 and Pulse Rate -
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SurgivetÂ® V1030 Hand-Held Pulse Oximeter

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