¦Patient range: adult, pediatric, neonatal. ¦24 hours ambulatory NIBP measure function, at best 358 pieces of ambulatory NIBP measure data can be recorded once. ¦Automatic measure and manual measure of the perfect combination, at best 300 pieces of NIBP measure data can be recorded once by manual measure.
¦High-definition color TFT display, strong visibility. ¦By data review interface such as "data list", "trend graph", "big font", NIBP data is clear at a glance. ¦The device can display low power prompt information, alarm information, error information and time information richly. ¦Supply two kinds of NIBP measure unit: mmHg / kPa. ¦Display interface can be switched between Chinese and English.
¦Parameter alarm dispose function is optional. ¦Communicate with PC, PC software can achieve data review, analysis measure results, seeing trend graph, printing reports and other functions. Measure Mode: The upper arm measure. Automatic Measure Interval: 18.104.22.168,240 minutes.
Measure range: 0kPa(0mmHg)~38.67kPa(290mmHg). ¦Display: 2.4 TFT colour LCD. ¦Alarm parameter: SYS / MAP / DIA. ¦Increasing pressure mode: force pump increases pressure automatically. ¦Reducing pressure mode: self-motion ladder reducing pressure mode.¦Power: DC 3V(Two "AA", 1.5V Alkali Battery). ¦Product safety type:Type BF applied part (Internally powered, defibrillation-proof). Dimension: 128mm69mm36 mm (No including Packing).
¦PC software is connect to the device by USB interface. ¦Can download NIBP measure result of the terminal device. ¦Can display scoop-shape trend graph, filling-type trend graph, histogram, pie chart, correlation line graph. ¦Can edit every piece of NIBP data, and add annotation to it.¦Can edit basic information, doctor's advice information, NIBP status instruction, current medicine-taken information, etc. ¦Support print preview, print the report. 1X Adult cuff, Adult Large cuff, child cuff. 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. This item is in the category "Business & Industrial\Healthcare, Lab & Dental\Medical & Lab Equipment, Devices\Blood Pressure Machines & Monitors". The seller is "contecmedical002" and is located in this country: US. This item can be shipped to United States, Canada, United Kingdom, Denmark, Romania, Slovakia, Bulgaria, Czech Republic, Finland, Hungary, Latvia, Lithuania, Malta, Estonia, Greece, Portugal, Cyprus, Slovenia, Sweden, Korea, South, South Africa, Belgium, France, Hong Kong, Ireland, Netherlands, Poland, Spain, Italy, Germany, Austria, Bahamas, Israel, New Zealand, Philippines, Singapore, Switzerland, Norway, Qatar, Kuwait, Bahrain, Croatia, Republic of, Malaysia, Colombia, Costa Rica, Antigua and Barbuda, Aruba, Belize, Dominica, Grenada, Saint Kitts-Nevis, Saint Lucia, Montserrat, Turks and Caicos Islands, Barbados, Bangladesh, Bermuda, Brunei Darussalam, Bolivia, Ecuador, Egypt, French Guiana, Guernsey, Gibraltar, Guadeloupe, Iceland, Jersey, Jordan, Cambodia, Cayman Islands, Liechtenstein, Sri Lanka, Luxembourg, Monaco, Macau, Martinique, Maldives, Nicaragua, Oman, Peru, Pakistan, Paraguay, Reunion, Vietnam, Uruguay.