Ambulatory Patient Monitor Vital Signs Monitor SPO2 NIBP HR PR 4 Parameters PM50

Description: PM50 Ambulatory Blood Pressure Monitor,Handheld Patient monitor DescriptionIntroductionPM50 is a multifunctional patient monitor, it can monitor SPO2 and NIBP for a long time, and applies to the hospital wards or family daily health.Features ◆Compact and portable, easy to use ◆With Integrative SpO2 Probe ◆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 ◆Case management function.PC software can achieve data review, analysis measurement results, seeing trend, printing reports and other functionsPerformance ◆NIBP Measurement Method: Oscillometry Measurement Mode: The upper arm measure Measuring range: ADULT: SYS 40mmHg～270mmHg MAP 20mmHg～235mmHg DIA 10mmHg～215mmHg PEDIATRIC: SYS 40mmHg～200mmHg MAP 20mmHg～165mmHg DIA 10mmHg～150mmHg NEONATAL: SYS 40mmHg～135mmHg MAP 20mmHg～110mmHg DIA 10mmHg～100mmHg Automatic Measurement Interval: 5.10.15.20.30.45.60.90.120 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 / MAP / 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:0bpm～250bpm Resolution:1bpm 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)Physics speciality Dimension: 128*69*36 mm (No including Packing) Weight: <350g (Including Batteries)Accessories ◆cuff for adult ◆Integrative SpO2 Probe for adult ◆USB data line◆Pouch ◆User manualSoftware function： ◆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.PaymentWe accept payment from PAYPAL, Bank transfer,Visa,Credit Card and others. All payments are expected within 7 days after the last winning auction is closed.ShippingClearance: we will ship your item to your Ebay confirmed address.Buyers' responsibility to pay duties,taxes and other extra charges by the government in your country.All items will be shipped within 2 business days by E-package,Airmail shipping.According to shipping method,items will be delivered within 7-35 days.We will do low value in PI,so that you can get items from your customs smoothly.Terms of SaleBuy safe ProductsThe following FDA Disclaimer is required for all eBay listing in Healthcare category and is included for REFERENCE: The sale of this item may be subject to regulation by the U.S. Food and Drug Administration and state and local regulatory agencies.If the item is subject to FDA regulation, We will verify your status as an authorized purchaser of this item before shipping of the item. 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 ApprovedAbout UsContec Medical Systems Co.,Ltd; 20 Years manufacturer,we have stock in USA and China.Contact UsContact Name:Karina; WhatsApp/Mobile:+86-13223300633; Email:contec001@gmail.com

Price: 179 USD

Location: Beijing

End Time: 2024-01-05T02:32:20.000Z

Shipping Cost: 0 USD