Description

Introduction

PM50 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 functions

Performance

   ◆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 manual

Software 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.

Payment

We 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.

Shipping

  1. Clearance: we will ship your item to your Ebay confirmed address.
  2. Buyers' responsibility to pay duties,taxes and other extra charges by the government in your country.
  3. All items will be shipped within 2 business days by E-package,Airmail shipping.
  4. According to shipping method,items will be delivered within 7-35 days.
  5. We will do low value in PI,so that you can get items from your customs smoothly.

Terms of Sale

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The 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 Approved

About Us

Contec Medical Systems Co.,Ltd; 20 Years manufacturer,we have stock in USA and China.

Contact Us

Contact Name:Karina; WhatsApp/Mobile:+86-13223300633;