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User’s Manual for UP-6000 multi-parameter patient monitor Instructions to User Dear Users, Thank you very much for purchasing our product. Please read the following very carefully before using this equipment. These instructions describe the operating procedures to be followed strictly. Failure to follow these instructions can cause monitoring abnormality, equipment damage and personal injury. The manufacturer is NOT responsible for the safety, reliability and performance issues and any monitoring abnormality, personal injury and equipment damage due to user’s negligence of the operation instructions. The manufacturer’s warranty service does not cover such faults. WARNING-PACEMAKER PATIENTS. Rate meters may continue to count the pacemaker rate during occurrences of cardiac arrest or some arrhythmias. Do not rely entirely upon rate meter ALARMS. Keep pacemaker patients under close surveillance. See this manual for disclosure of the pacemaker pulse rejection capability of this instrument. Monitoring a single person at a time. The monitor is defibrillator proof. Verify that the accessories can function safely and normally and the monitor is grounded properly before conducting defibrillation. Disconnect the monitor and sensors before MRI scanning. Use during MRI could cause burns or adversely affect the MRI image or the monitor’s accuracy. If you have any doubt to the grounding layout and its performance, you must use the built-in battery to power the monitor. All combinations of equipment must be in compliance with standard of IEC 60601-1-1 for medical and electric system requirements. Check SpO 2 probe application site periodically (every 30 minutes) to determine circulation, positioning and skin sensitivity. The SpO 2 measurement of this monitor may not work for all testees. If stable readings cannot be obtained at any time, discontinue using. Do not immerse the monitor or its accessories in liquid to clean. Do not use accessories manufacturer. other than those provided/recommended by the Each time the monitor is used, check the alarm limits to ensure that they are appropriate for the patient being monitored. The monitor is intended only as an adjunct in patient assessment. It must be used in conjunction with clinical signs and symptoms. When taking the measure of a pediatric or neonate’s (less than 10 years old) blood pressure, do NOT operate in the adult mode. The high inflation pressure may cause lesion or even body putrescence. II