Volumetric Infusion Pump IV Fluid equipment Syringe Pump SP750 Audio Alarm KVO

Description

002 梅花
SP750 Volumtric 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
2.Bank transfer
Shipping
Clearance: 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 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 USA. Inc.
1440 Chase Ave,
Elk Grove Village, IL, 60007-4825,United States
Contact Us
WhatsApp/Mobile:86-18716007715;contecmxfATgmail.com
We only have the English Manual in the standard package, If you need any other language Manual, please contact us freely