3The time segment of dealing with the patient's NIBP data is 48 hours. 4Connect the device by USB interface. 5Can upload patient information data collection project and download collection data. 6Can display scoop-shape trend graph, filling-type trend graph, histogram, pie chart, correlation line graph.7Can edit every piece of data, and add annotation to it. 8Can edit basic information, doctor's advice information, NIBP and SpO2 status instruction, current medicine-taken information, etc. 9Support print preview, print the report. NIBP: Measurement Method: Oscillometry Measurement Mode: The upper arm measure Measuring range: SYS 40mmHg~270mmHg MAP 20mmHg~235mmHg DIA 10mmHg~215mmHg Automatic Measurement Interval: 18.104.22.168.22.214.171.124.120 minutes Resolution: 1mmHg Accuracy: ±3mmHg Increasing pressure mode: force pump increases pressure automatically Reducing pressure mode: self-motion ladder reducing pressure mode Alarm parameter: SYS / DIA SpO2: Measuring range: 0%~100% Resolution:1% Accuracy: 70-100%, ±2%, below 70% unspecified Error in Weak Filling Condition:SpO2 and pulse rate can be shown correctly when pulse-filling ratio is 0.4%. SpO2 error is ±4%, pulse rate error is ±2 bpm or ±2% (select larger). Resistance to surrounding light:The deviation between the value measured in the condition of man-made light or indoor natural light and that of darkroom is less than ±1%. Pulse Rate: Measuring range:30bpm250bpm Resolution:1bpm Accuracy: ±2 bpm or ±2% (select larger) Display: 2.4" TFT colour LCD Safety: Power: DC 3V(Two "AA, 1.5V Alkali Battery) Product safety type:Type BF application part (Internally powered, defibrillator protected). Cuff for adult Integrative SpO2 Probe USB data line Disk (PC software) Pouch User manual. Dimension: 1286936 mm (No including Packing) Weight. Food and Drug Administration and state and local regulatory agencies. If you have questions about legal obligations regarding sales of medical devices, you should consult with the FDA's Center for Devices and Radiological Health. The Fingertip Pulse Oximeter is registered on the Australian Register of Therapeutic Goods (ARTG) with the code 197923, and certified by FDA of United States and CE, TUV of Europe. The Fingertip Pulse Oximeter that is FDA 510K Approved. Our product line covers a wide range of 13 categories. Most of the domestic hospitals are our customers. Contec hopes to cooperate with international companies to supply more innovative design and advanced technology products We sincerely welcome you to become one of our global partners. We are looking forward to establishing a successful business relationship with you. ECG / ECG holter EEG / EEG Holter B-ultrasound. Patient Monitor Fetal doppler Fetal Monitor.
Spo2 Monitor Stethoscope Medical Image... All emails will be answered within 24 hours on weekdays(but within 48hours on weekends). Communication is KEY to helping us give you the best experience. We will do our best to turn any less than satisfactory experience into a positive one.Welcome to my store please contact me and give you a 10% discount. This item is in the category "Business & Industrial\Healthcare, Lab & Dental\Medical & Lab Equipment, Devices\Patient Monitors". The seller is "qiuyu_4054" and is located in this country: CN.
This item can be shipped worldwide.