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)High-precision infusion control ensures an accurate and safe infusion.

2)Be compatible with multiple IV set brands, the new IV set can be calibrated, ensures infusion accuracy.

3)Display infusion parameters (such as accumulated volume, remaining time) by the 2.8'' high-definition color LCD, convenient for clinical observation.

4)Air bubble detection technology, avoids missing alarm or detection effectively, reduces potential risks.

5)With rate, time, gradient ,drip and other working modes, satisfies clinical needs.

6)Independent audible and visual alarm, more than 10 kinds of alarms, and the alarm priority is distinguished by colors, ensures a safe infusion.

7)Adjustable occlusion thresholds, meets different pressure needs, ensures a safe infusion.

8)Avoidance of free flow of liquid, the use of new clamp avoids free flow of liquid when the door is opened. 

9)Support drug library function, where users can set the common drugs, easy to operate.

10)Large-capacity memory, the treatment history can be reviewed at any time.

11)After preset volume is completed, it will operate at KVO rate, which is adjustable.

12)Intelligent dual-way power supply systems, the built-in high capacity lithium battery achieves uninterrupted infusion.

13)Connect with workstation and central management system to achieve centralized data management. 


Performance

Type: volumetric infusion pump  

Infusion rate: 0.1 ~ 1200 mL/h, increment: 0.1 mL/h  

Total volume: 1 ~ 9999 mL, increment: 1 mL

Accuracy: ± 5 % (use the IV set calibrated)

Display information: ①Rate②Pressure③Drug name④remaining time⑤VTBI/Volume

Safety classification: class I, type BF applied part

Waterproof degree: IPX2

Operation mode: continuous operation

Alarm functions: The door open、Motor abnormal、Pressure abnormal、The infusion tube is blocked、Air bubble in IV tube、Enter KVO mode、Battery exhausted、Infusion will over、Reminder、Low battery、Communication Error

Air bubble detector: ultrasonic

TFT: 2.8'' 

KVO rate: 0.1 ~ 5 mL/h, increment: 0.1 mL/h

Sensitivity for pressure sensor: 1~5 grades (it can be adjusted by professional medical staff)

Special safety measures: 

1)The use of new clamp avoids free flow of liquid when the door is opened accidentally. 

2)Air bubble detector with high accuracy prevents air bubbles from entering patient’s body.

3)Pressure sensor prevents occlusion for IV set.

4)With password protection function (in system parameter setting and IV set type interface).


Accessories

◆ A power cord

◆ A user Manual


Physical characteristic

Dimension: 260 mm (L) × 136 mm (W) × 88.8 mm (H)

Weight:about 1.9 kg

Working environment: 

Temperature: + 5 ℃ ~ + 40 ℃ 

Relative humidity: 20 % ~ 90 %

Atmospheric pressure: 800 hPa ~ 1060 hPa

Storage environment: 

Environment temperature: - 30 ℃ ~ + 55 ℃ 

Relative humidity: 5 % ~ 96 % 

Atmospheric pressure: 500 hPa ~ 1060 hPa 

No corrosive gas 

Well-ventilated

Power supply: 100-240V~, 50/60 Hz, rechargeable lithium battery, 7.4 V/5000 mAh

Input power: 25 VA

Shipping

    1. Clearance: we will ship your item to your confirmed address.
    2. Buyers' responsibility to pay duties,taxes and other extra charges by the government in your country.

Terms of Sale

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. 
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:Tessy Zhang; Whatsapp/Mobile:+86-18716007715; contecmxfATgmail.com