24 hours multifunctional patient monitor,SPO2/NIBP/Pulse Rate PM50 

Introduction

PM50 is a multi-functional patient monitor that can monitor BP and SpO2 at  the same time. Realizing long time monitoring of dynamic blood pressure, the device is widely applicable to hospital wards, community clinics  and other medical institutions.

Functions

Features:

1)Compact and portable, easy to use.

2)With Integrative SpO2 Probe.

3)Double working modes,monitoring function and 24 hours ambulatory NIBP measurement function can be flexibly set.

4)Long time monitoring BP and SpO2, displaying value of BP, SpO2 and PR.

5)NIBP and SpO2 data Record for large capacity.

6)With friendly user interface, the user can see list menu and review measurement results.

7)The device can display low power information, alarm information, error information and time information richly.

8)Parameter alarms function is optional.

9)Patient information can be flexibly set.

10)Case management function.PC software can achieve data review, analysis  measurement results, seeing trend, printing reports and other functions.

11)Data can be transmitted between device and computer, such as upload patient information, download measurement data.

12)English and Chinese menu.

Function of master device software:

1）Set patient information through PC software.

2）Up to 1000 patients cases can be edited and supervised.

3）The time segment of dealing with the patient’s NIBP data is 48 hours.

4）Connect the device by USB interface.

5）Can upload patient information data collection project and download collection data.

6）Can display scoop-shape trend graph,filling-type trend graph, histogram, pie chart, correlation line graph.

7）Can edit every piece of data, and add annotation to it.

8）Can edit basic information,doctor's advice information, NIBP and SpO2  status instruction, current medicine-taken information, etc.

9）Support print preview,print the report.

Performance

NIBP：

• Measurement Method: Oscillometry
• Measurement Mode: The upper arm measure
• Measuring range: 
•        SYS   40mmHg～270mmHg
•        MAP  20mmHg～235mmHg
•        DIA   10mmHg～215mmHg
• 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 / 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:30bpm~250bpm
• 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）< /div>
• Product safety type:Type BF application part (Internally powered,defibrillator protected)

Accessories

• cuff for adult
• Integrative SpO2 Probe
• USB data line
• PC software to be download from the website
• Pouch
• User manual

Physical characteristic

• Dimension: 128*69*36 mm (No including Packing)
• Weight: <350g (Including Batteries)
• Working environment:
• Temperature：5 ˚C～40 ˚C
• Relative humidity：≤80%
• Altitude：-500 to 4,600m (-1,600 to 15,000ft)
• Specific EMC, climate, mechanical environment: Do not use a mobile phone in the  vicinity of the patient monitor for the strong radiation field produced  by  mobile phone would interfere with the normal function of the patient monitor use.
• Storage environment:
• Temperature： -20˚C ~ 60 ˚C
• Relative humidity： ≤95 %
• Altitude：-500 to 13,100m (-1,600 to 43,000ft)
• Specific EMC, climate, mechanical environment: The patient monitor after  packaged should be stored in a well-ventilated room with no corrosive  gas. Strong shock, vibration and snow and rain should be avoided during  transportation.

• Buy safe products  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.  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