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
2.Bank transfer
Shipping
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
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
1440 Chase Ave,
Elk Grove Village, IL, 60007-4825,United States