Volumetric Infusion Pump IV Fluid Syringe Pump Equipment Alarm Calibration SP750

Description

Test Item
Volumetric Infusion Pump IV & Fluid Syringe Pump Equipment Alarm & Calibration
SP750 Infusion Pump
Description
Introduction
The product is a  volumetric infusion pump, features in high safety, easy operation and long life.  Flow control with high accuracy and comprehensive alarm measures ensure  patient's safety and optimum therapeutic effect.
Function
1) Flow control with  high accuracy ensures optimum therapeutic effect.
2) Be compatible with most  standard IV Sets.
3) New IV set provided by user can be calibrated by  suppliers, and infusion parameters can be input into the pump, which ensures  accuracy.
4) 3.5'' TFT-LCD.
5) Operate with keys.
6) Residual infusion  time can be displayed during infusing.
7) With reminder function for starting  infusion.
8) Alarm for occlusion, air bubble, door open and motor failure,  etc.
9) Threshold for air bubble and pressure alarm can be adjusted by  medical personnel.
10) Accompanying IV-set clamp prevents liquid flowing  freely when the pump door opens accidentally.
11) A.B.S——ANTI BOLUS system  prevents instantaneous high-dose injection from the sudden obstruction  disappearing.
12) Stop infusing automatically during alarm(except for "NEAR  END", "KVO", and "LOW BATTERY" alarms).
13) Alarm volume can be  adjusted.
14) Power supply: AC/DC and built-in lithium battery.
15)  Compact aluminum enclosures and robust construction.
16) USB port is  convenient for technical personnel to update software..
17) Infusion pump can  be mounted on infusion pole in many directions by the versatile bracket.
18)  Infusion parameters can be saved after power off.
Performance
◆ Type: volumetric  infusion pump
◆ Infusion rate: 1~699ml/h, increment: 1ml/h
◆ Total volume:  1~9999ml/h, increment: 1ml/h
◆ Accuracy: ±5%(use the IV set calibrated)
◆  KVO rate:1~5ml/h(it can be adjusted by professional medical personnel)
◆  Display information: flow rate, total volume, accumulated infusion volume,  residual time
◆ Alarm functions: near end, KVO state, low battery, no power,  pressure failure, door failure, air bubble, door open, occlusion, infusion  reminder, communication failure and motor failure.
◆ Air bubble detector:  ultrasonic
◆ Sensitivity for air bubble detector: 0.01~0.14ml(it can be  adjusted by professional medical personnel)
◆ Sensitivity for pressure  sensor: 1~7 grades(it can be adjusted by professional medical personnel)
◆  Safety classification: class I, type BF applied part
◆ Waterproof degree:  IPX1
◆ Working mode: continuous working
◆ Power supply: AC:100~240V,  50/60Hz or DC: 12V
Rechargeable Li-polymer battery, 7.4  V/3500mAh
Special safety measures:
◆ Accompanying IV-set clamp prevents  liquid flowing freely when the pump door opens accidentally.
◆ Air bubble  detector with high accuracy prevents air bubbles from entering patient’s  body.
◆ Pressure sensor prevents occlusion for IV set.
◆ A.B.S system,  when the high-voltage occlusion alarm appears, stop infusing immediately, and  eliminate the pressure of the IV set automatically, which prevents instantaneous  high-dose injection from the sudden obstruction disappearing.
◆ Infusion  parameters during infusing are protected against being changed arbitrarily.
◆  With password protection function(in system parameter setting and IV set type  interface).
Accessories
◆ A versatile bracket
◆ A power cord
◆ A user Manual
Physical  characteristic
Dimension: 197 mm(L)×145 mm(W)×135  mm(H)
Weight: 2 Kg
Payment
1.Paypal account
Shipping
Clearance: we will ship your item to your confirmed address.
Buyers' responsibility to pay duties,taxes and other extra charges by the government in your country.
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
Whatsapp/Wechat:+86 18716007715; Skype:contec.tessy; contecmxfATgmail.com
Only English user guide, if you need any other language, please contact us!
Only English user guide, if you need any other language, please contact us!