Compact and portable, easy to use. Double working modes, monitoring function and 24 hours ambulatory NIBP measurement function can be flexibly set. NIBP and SPO2 can be monitored for a long time. NIBP and SPO2 data Record for large capacity. With friendly user interface, the user can see list menu and review measurement results.The device can display low power information, alarm information, error information and time information richly. Parameter alarms function is optional. Patient information can be flexibly set. PC software can achieve data review, analysis measurement results, seeing trend, printing reports and other functions. Measurement Mode: The upper arm measure.
Automatic Measurement Interval: 18.104.22.168.22.214.171.124.120 minutes. Increasing pressure mode: force pump increases pressure automatically. Reducing pressure mode: self-motion ladder reducing pressure mode.Alarm parameter: SYS / MAP / DIA. 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).
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%. Accuracy: ±2 bpm or ±2% (select larger). Display: 2.4 TFT colour LCD.Power: DC 3V(Two "AA", 1.5V Alkali Battery). Product safety type:Type BF application part (Internally powered, defibrillator protected).
Dimension: 1286936 mm (No including Packing). Integrative SpO2 Probe for adult. Up to 1000 patients cases can be edited and supervised. The time segment of dealing with the patient's NIBP data is 48 hours. Connect the device by USB interface.Can upload patient information data collection project and download collection data. Can display scoop-shape trend graph, filling-type trend graph, histogram, pie chart, correlation line graph. Can edit every piece of data, and add annotation to it. Can edit basic information, doctor's advice information, NIBP and SpO2 status instruction, current medicine-taken information, etc. Support print preview, print the report.
The sale of this item may be subject to regulation by the U. 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. Contact Name:Karina; WhatsApp/Mobile:+86-13223300633.
This item is in the category "Business & Industrial\Healthcare, Lab & Dental\Medical & Lab Equipment, Devices\Patient Monitors". The seller is "medicalcare4u" and is located in this country: CN. This item can be shipped to United States, all countries in Europe, all countries in continental Asia, Brazil, Canada, Australia.