covetrus ProMAX IV User manual

User Manual
Infusion Pump for Veterinary Use
ProMAX IV
Touch Digital Infusion Pump

Table of Contents
Preface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Application Scope . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Use Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Paraphrase . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Description of Revision of User Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Safety Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2
Cautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Dialogue Windows . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Application Scope . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Expected Purpose . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Expected Working Environment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Working Principle . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Structure and Performance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Structure and Performance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Product Specification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5
Appearance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Front View . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8
Operation Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9
Rear View . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10
Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Unpacking and Checking . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Install the Covetrus® ProMAX IV Touch Digital Infusion Pump . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11
Use Preparation & Cautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Use Preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Operation Cautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Basic Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Operation Flow . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Infusion Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Equipment Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Starting and Self-test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Infusion set Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Purge Air . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Start Infusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Changing the Rate During Infusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Bolus Application . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Infusion Completion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Stop Infusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Remove the Infusion Set . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Power off or Standby . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16
Replace Infusion Set/Infusion Container . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16

Table of Contents
Set Infusion Parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Introduction to Infusion Parameters Setting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Infusion Mode Setting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Rate/Time Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Body Weight Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Drug Library Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
Sequence Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17
System Setting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Infusion Set admin brands . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Cage No . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Drug Library . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
KVO Rate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Bolus Rate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Occlusion Pressure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18
Pressure Unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Bubbles Size . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Pump Idle Alert . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Finish Pre-Alarm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
Micro Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Reset Total Volume . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Rotate Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Date & Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Brightness . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Sound . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Screen Lock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Night Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Battery capacity display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Language . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20
Factory Default . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Version . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Maintenance Period . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Last Maintenance Date . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Other Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
History Entries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Last Therapies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Anti-bolus . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Alarm Prompt and Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Introduction to Alarm Level . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Multilevel Alarm Rules . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Alarm Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Fault Analysis and Solution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22

Table of Contents
Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Periodical Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Appearance Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Performance Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Maintenance Plan . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Repair . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Normal Repair Process . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Maintenance for Long-Term Store . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Equipment Components/Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Production Date . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Recycling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Check Battery Performance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
Replace Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
After-Sale Service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
Appendix . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Appendix A Alarm and Solution. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26

1
Preface
Application Scope
Applicable to the Covetrus® ProMAX IV Touch Digital Infusion Pump.
This user manual describes the product's most complete configuration. For more detailed information,
please contact Covetrus.
Use Instructions
This user manual covers the basic information on the safety and effectiveness of the product for guiding
the operator to correctly install, test, operate, use, and maintain the product. Please read this manual
thoroughly before use to ensure correct usage and carefully store it for future use.
Covetrus is responsible for the reliability and performance of the equipment only if all the following
conditions are met:
1. Use the equipment according to this user manual.
2. The equipment can only be disassembled, assembled, replaced, tested, improved, and repaired by
Covetrus or Triumph Medical.
3. All components and accessories, as well as consumables for repair, are provided by Covetrus or
Triumph Medical.
Paraphrase
Mechanical button
Touch button
( ) Information
- Inapplicable
√ Accordant
→Operation steps
Bolus: Infuse large volume of liquid in a short time.
KVO: Keep vein open, prevent blood back to the Infusion set.
Anti-bolus: Motor automatically reverses when there is high pressure.
Accessories: suitable for use with the equipment in order to achieve the expected purpose or provide
convenience for attaining the desired purpose.
Description of Revision of User Manual
This manual may be revised occasionally as product improvements are made, etc. All revisions will be
documented in the new version of the instructions.

2
Safety Instructions
Warnings
Before using, please check the equipment, connecting wire, and accessories to ensure they can work
normally and safely. If there's anything abnormal, immediately stop working and contact Triumph Medical.
Additionally, the adhesion or intrusion of fluid/drug may cause the equipment to fault and malfunction.
Therefore, please clean the equipment after use, and store it correctly.
It is not allowed to store or use the equipment in an environment with active chemical gas (including gas
for disinfecting) or a moist environment since it may influence the inside components of the Covetrus®
ProMAX IV Touch Digital Infusion Pump and may cause performance drop or damage to the inside
components.
If the infusion set is twisted, the filter or needle is obstructed, or blood in the needle which may obstruct the
infusion, the pressure in the infusion set will rise. Removing such occlusion may cause a "bolus infusion"
(temporary excess infusion) to the animal. The correct method is to tightly hold or clamp the infusion set
near the puncturing position, then open the door to drop the pressure in the infusion set. Then loosen the
infusion set, solve the reason for occlusion, and restart infusion.
During infusion, please periodically check the dripping state of the fluid and the fluid/drug in the
intravenous infusion bag/container to ensure the pump is working correctly during infusion. Therefore, this
equipment doesn't directly measure the quantity of the infusion fluid. It is possible that this equipment can't
detect the free infusion flow under exceptional conditions.
Tightly fix this equipment on the infusion stand and ensure its stability of the infusion stand. Be careful
when moving the infusion stand and this equipment to avoid the equipment dropping and infusion stand
falling or knocking the surrounding objects.
This equipment injects fluid/drug through extruding the infusion set, but it can't detect the leakage if the
infusion set is cut off or broken. Therefore, please periodically check it to avoid above fault during the
working period.
It is not allowed to put and use the equipment in the environment with anesthetic and other inflammable or
explosive articles to avoid fire or explosion.
Please correctly install the infusion set according to the infusion indication direction of this equipment and
ensure that the infusion set is placed smoothly and straight across the creep device.
If the sound level of the alarm signal is lower than the environmental noise, the operator may not hear the
alarm.
This equipment has an occlusion detection function for detecting and alarming when the infusion needle
deviates from the position in the vein or the needle is not correctly punctured in the vein.
To avoid the risk of electric shock, this equipment must only be connected to a supply main with
grounding.
Disassembling or refitting this equipment or
using it for other purposes except normal
infusion is prohibited.
No one is allowed to repair this equipment
except Triumph Medical.
Please do not depend only on the alarm system during use; please periodically check it to avoid an
accident.

3
Cautions
Dialogue Windows
Dialogue window mainly includes operation select, operation confirm, and information.
Before its first use after purchase, or if the equipment is not used for a long period, please charge the
equipment with AC power supply. If it is not fully charged, under a power failure, the equipment may not
continue to work with built-in battery power supply.
Under general conditions, please use AC power supply as much as possible since it can prolong the service
life of the battery to a certain degree. When using AC power supply, ensure that the grounding wire is
reliably connected to the ground, and only the AC power cord attached to this equipment shall be used.
Please pay attention to the plug position of the power cord to ensure that you can disconnect it at any time.
The built-in battery can only be used as an assistant power supply when the AC power supply can't
reliably connect with the ground and is not under normal conditions (power failure or in-transport infusion).
Before connecting this equipment with the power supply, please keep the power socket and plug dry. The
power voltage and frequency must meet the requirements listed on the equipment label or in this User
Manual.
The equipment is equipped with an audible and visual alarm system, the red and yellow alarm indicators will light on
by turn, and the speaker makes the "beep" sound.
Please use the fluid/drug after it has reached or nearly reached room temperature. When the fluid/drug is
used at low temperatures, the air which is dissolved in the fluid/drug may cause more air bubbles and
result in frequent air bubble alarms.
It is not allowed to press and operate the button with a sharp object (such as a pencil tip and nail). Otherwise, it may
cause early damage to the button or surface lm.
Please do not use the same infusion set over 8 hours at the same pumping position. Infusion set may
distort after use for a long time and cause a flow rate error. It is suggested to replace the pumping position
or directly replace the infusion set once every 8 hours.
Under the condition of low flow rate infusion, please pay particular attention for an occlusion. The lower
the infusion flow rate, the longer the time to detect an occlusion, which may cause a long-time infusion
stoppage during this period.
If the equipment is damaged from dropping or impact, please stop using it immediately, and contact
Covetrus®. The equipment's inside components may be damaged even if the appearance is not damaged
and abnormality does not occur when working.
Please tightly close the ow rate adjuster of the infusion set before taking out the infusion set to avoid infusion free
ow.
When using this pump, other infusion control equipment cannot be installed on the same infusion tube. Otherwise, it
may cause errors.
Please keep the equipment at a certain distance from the AC power socket to prevent the chemical liquid from
splashing or dripping into the socket and causing a short circuit fault.

4
Symbols
Not all of the below symbols exist in the equipment you have purchased.
Lot Number
Attention, consult
accompanying documents
Both direct and alternating current
Environment-friendly use period
(20 years)
Date of Manufacture
Bell, cancel temporary
Serial Number
Protective earth
Alternating Current
Input and output
Handle with care
Manufacturer
Selection; affirmative
acknowledgement; success; ACK
Ingress Protection
(Prevent solid objects larger than 2.5
mm in diameter and water intrusion
from splashing in all directions)
Marks Description Marks Description
IP34
SN

5
Overview
Application Scope
Expected Purpose
This product is used for constant-speed intravenous infusion in a hospital.
Expected Working Environment
Including but not limited to the operation room and surgery table in an animal hospital/or pet clinic.
Working Principle
This equipment can drive a pump to extrude the infusion set for accurately controlled infusion drops or
infusion flow rate with the motor. It is capable of guaranteeing the infusion of drug fluids safely in the
vein of animals with an even rate and accurate dosage.
Structure and Performance
Structure and Performance
The Covetrus® ProMAX IV Touch Digital Infusion Pump is composed of the main unit and built-in battery,
which can be subdivided into shell assembly, main control module, power module, display module,
operation module, drive module, monitoring module, and alarm module.
This equipment provides several infusion modes, such as rate mode, time mode, body weight mode, drug
library mode, and sequence mode. Additionally, it also has functions such as history records, drug library,
Anti-bolus, alarm, and so on.
Accessories
Power Cord and Pole Clamp.
Product Specification
Ingress Protection IP34 (Prevent solid objects larger than 2.5 mm in diameter and water intrusion
from splashing in all directions)
Working mode Continuous
Classification Portable equipment, non-portable infusion pump
Safety Classification
Infusion Set Specification 10~60 drops
System Accuracy ±5%
Drip Infusion Rate Accuracy ±10% or ±1 drops/minute
Infusion Rate 0.10-1500 ml/h
Drip mode range 1~500 drops/minute
Bolus Rate 0.1-1500 ml/h
Specification Parameters

6
Bolus preset 0.1-60 ml
KVO Rate 0-5.00 ml/h
Micro Mode Setting Range 100-1500 ml/h
Minimum Flow Rate Increment 0.01 ml/h
VTBI 0-9999.99 ml, minimum step is 0.01 ml
Total Volume Infused 0.01-9999.99 ml, minimum step is 0.01 ml
Time Range 1 minute - 99 hours 59 minutes
Fuse Type slow fuse 2A 250V
Dimensions 105(w) x 109(d) x 142(h) mm (Pole Clamp not included)
Weight 1.4 kg, 3.08 lbs
Specification Parameters (continued)
AC Power Supply 100-240V 50/60Hz
Input Power 20VA
DC Power Supply DC 12V
Battery Specifications Specification: 7.4V 2500mAh
Charging time: single battery less than 2 hours, two batteries less than 4 hours
(under OFF status)
Working time: single battery over 4.5 hours, two batteries over 9 hours
(after completely charging battery/batteries, when the environment temperature
is 25°C or 77° F and flow rate is 25 ml/h, the constant working time)
Power Supply
Alarm Signal Sound Pressure Level When the sound is set at lowest level, alarm signal sound pressure level ≥45dB(A)
When the sound is set at highest level, alarm signal sound pressure level ≤80dB(A)
Alarm Information VTBI near end, VTBI infused, Occlusion (Pressure high), Battery nearly empty,
Battery empty, No battery inserted, No external power supply, Pump idle alarm,
Standby time expired, KVO finished, Air bubble, Door Open
Alarm

7
Non-AP/APG type equipment Do not use it in an environment with inflammable anesthetic gas mixed with air,
and inflammable anesthetic gas mixed with oxygen or nitrous oxide
Operating 1. Temperature: 5–40°C, 41–104°F
2. Humidity: 20-90%, non-condensable
3. Atmospheric Pressure: 57-106kPa
Transport and Storage 1. Temperature: -20–55°C, -4–131°F
2. Humidity: 10-95%, non-condensable
3. Atmospheric Pressure: 50-106kPa
Environment

8
Appearance
Front View
Part Number Name
①Tubing Guide
②Pump Door Air Bubble Sensor (for air bubble detection in the infusion line)
③Pump Tablets
④⑦ Pressure Plate
⑤Pump Door
⑥Pressure Sensor (for occlusion detection)
⑧Anti-Free Flow Clamp

9
Operation Panel
Part Number Name
①Touch Screen
② Power Pump power switch, short pressing the power button
to enter the shutdown setting interface, the user can
set shutdown, standby (time), or cancel.
Long pressing the power button until the screen turns off.
③ Home Enter system home page.
④ Bolus/Purge
⑤ Start/Stop
⑥Running Indicate Light
⑦ Alarm Indicator Light While pump alarms, the indicator light flashes with
different frequencies and colors to show different alarm
levels. For more information, please refer to page 21.
⑧AC Indicate Light When connected to the AC power supply, the AC
indicator light is on.

10
Rear View
Part Number Name
①DC Input Port, external 12V DC power supply
②Multi-function USB Port
③A/C Adapter Port, external 100-240V 50/60Hz AC power supply
④Loudspeaker
⑤Pole Clamp, used for fixing the equipment on the infusion stand
⑥Handle

11
Installation
Unpacking and Checking
• Please check the appearance before unpacking; if broken, please contact Covetrus®.
• Please carefully open the package to avoid damaging the equipment and relevant accessories.
• After unpacking, please check the objects according to the packaging list; if there are insufficient or
damaged accessories, please contact Covetrus.
• Please keep relevant accessories, warranty card, and User Manual.
• Please keep the packing case and packing materials for future transportation or storage.
Installation
Install the Covetrus® ProMAX IV Touch Digital Infusion Pump
• Rotate the Pole Clamp screw (knob) and unscrew it to leave space
• Lock the Pole Clamp on the infusion stand, adjust the position of the ProMAX IV Touch Digital Infusion
Pump, and tighten the Pole Clamp to fix the ProMAX IV on the infusion stand (as shown in the
drawing).
• Hold the ProMAX IV when tightening the fixing clamp; carefully let go of it after tightening to avoid it
from falling
• The Pole Clamp supports the vertical pole at the default state. To adjust the Pole Clamp direction,
please remove the bolt from the Pole Clamp, take out the Pole Clamp and, adjust the direction, then
tighten the bolt
Please put the packing materials out of reach of children. Please obey local laws and regulations when
disposing of items.
•This equipment shall be installed per instructions of this manual
•When connecting this equipment with other electric devices to form a combination with special function,
if the combination can't be confirmed dangerous or not, please contact Covetrus or an electrical expert
of the hospital to ensure the necessary safety of all devices in the combination won't be destroyed
•This equipment must be used and stored in an environment that satisfies the guidelines from this manual

12
Use Preparation & Cautions
Use Preparation
If the equipment is new, reusing after storing for an extended period, or reusing after repair, please
check it to ensure before use:
• The equipment's appearance is clean and in good condition without cracks and leakage
• The moving components are smooth and effective; the buttons are effective
• The touch screen can be operated smoothly and effectively
• The power cord is installed tightly and won't be easily damaged when pulling
• Set and check the system time to ensure the history records will be correctly recorded
• If only the built-in battery is adopted for supplying power, please charge it fully before using,
and check the battery state frequently
• Carefully read the Warnings, Cautions, and Operation Steps in this User Manual
Operation Cautions
•Avoid direct sunlight, high temperature, and high humidity
•The parameters can only be set or changed by trained and professional personnel
•Infusion accuracy or abnormal work of the equipment may be compromised if the working environment
temperature exceeds the designated range
•The viscosity and specific gravity of infusion fluid will influence infusion accuracy

13
Basic Operation
Operation Flow
• Mount the Covetrus® ProMAX IV Touch Digital Infusion Pump on the IV stand: refer to page 11
• Power on: press button to power on, and the machine completes a self-inspection; refer to below
• Install Infusion set: refer to below and page 14
• Confirm Infusion set brand name: Select infusion set brand
• Remove air bubble from the line: refer to page 14
• Select infusion mode: Select infusion modes according to requirement
• Set infusion parameters: set infusion parameters according to requirement
• Connect the infusion set with the animal
• Start infusion: press , start infusion
• Finish infusion: refer to page 15
• Remove the Infusion set: refer to page 16
• Power off or Standby: refer to page 16
Infusion Operation
Equipment Installation
Mount the device on the infusion stand according to page 11, connect with AC power supply, and
check the AC indicator lights. The battery will start to charge once AC power is connected.
Starting and Self-test
• Press button to power on the equipment
• After power is on, the system will automatically check the motor, sensor, battery, memorizer,
CPU communication, and alarm indicator
• After passing the self-test, the pump enters into rate mode interface
Infusion Set Installation
If the self-test fails, the pump cannot be operated properly or is damaged, it cannot be used for animal
infusion; please contact Covetrus®.

14
Infusion set Installation (continued)
• Connect the IV set with the infusion bottle
• Extrude the drip chamber
• When the fluid has reached the 1/2 position of the drip chamber, open the adjuster
• Fill fluid/drug to the injection needle to remove air, then close the adjuster
• Pull the lock switch in the middle of the Pump Door from the lower side, then open the door
• Push the Anti-Free Flow Clamp up to open it
• Install the infusion set in the slot according to the direction indicator shown in the above drawing,
and press the infusion set in the pump inwards to make it attach to the peristaltic pump
• Manually push the Pump Door, which will make a "click" sound after it is correctly closed
• Click 『Settings』→ 『Commonly used tube brand』, and select infusion set brand
Purge Air
There are two ways to set parameters for purging air: manual purge and automatic purge. Users can
choose the method according to their needs, and the total purge volume is not calculated in the Total
Volume Infused.
• Manual purge: Long pressing [Bolus] button , the device will purge air according to the default
flow rate of the system, release it and return to the setting parameter interface
• Automatic purge: Under the parameters setting interface, Press 【Bolus】 button on the
display and select "Yes" in the pop-up prompt box until the air bubbles in the infusion line are
eliminated and click "Stop"
Start Infusion
Connect Infusion set to animal, confirm infusion parameters, Press【Start】 button , click『 』
in the pop-up prompt interface, start infusion.
•Before purging air, double-check to confirm the infusion set is not connected with the animal
•Purge rate is the max rate. The purge will automatically stop when the volume is ≥ 5 ml
•It is suggested to use the infusion set brand defaulted in the pump
•Please confirm that the infusion set brand and specification displayed on the display screen is
accordant with the actual one in use
•Contact Triumph Medical if you are unsure if you are selecting the correct infusion set brand–selecting
the wrong infusion set brand could compromise the accuracy and possibly cause injury to the patient
Yes

15
Changing the Rate During Infusion
During the infusion process, the flow rate/dose rate/drop rate can be changed without stopping in any
infusion modes.
Bolus Application
During operation, the bolus functions have two operation modes: Manual bolus and Automatic bolus.
• Manual bolus: Long pressing the 【Bolus】 button on the product panel, pump will work at the
•
max flow rate (refer to 2.5). Once the button is released, the pump will return to the previous infusion
rate
Automatic bolus: Under the running interface, click the 『Bolus』 button on the touch screen, set
two parameters among bolus infusion volume, rate, and time, and click『Start』. It will beep at every
1ml infused. After the bolus infusion is finished, it will return to the previous infusion rate
Infusion Completion
When the remaining infusion time is near the preset volume to be infused completion time, the pump will
alarm. If the alarm is ignored, the system will keep alarming until it completes the VTBI infusion. For more
information, please refer to page 19
After VTBI is completed, it activates VTBI infused alarm. If the KVO function is ON, the equipment
automatically starts the KVO function click『OK』in the alarm interface to stop KVO and eliminate the
alarm.
The default working time of the KVO system is 30min. After reaching that time, it will activate the KVO
completion alarm and stop infusion.
Please refer to page 18 to set the KVO rate.

16
Stop Infusion
During infusion, click infusion stop. It will return to the parameter setting interface and display
Total Volume Infused and adjustable parameters.
Remove the Infusion Set
Disconnect the infusion set from the animal, and open the Pump Door manually, the liquid can still be
stopped normally with the Anti-Free Flow Clamp, and the infusion set can be removed after the
Anti-Free Flow Clamp is opened.
Replace Infusion set; please follow the steps on page 14.
Power OFF or Standby
Method 1: Hold the 【Power】Button till the screen is OFF, the equipment is OFF.
Method 2: Press 【Power】Button to enter into the power OFF interface.
• Power off the equipment: click the『Power off』icon, and the equipment is turned OFF
• Standby: click the『Standby』icon to enter into standby time setting interface, and set the standby
time. Under standby state, the screen brightness will be at its lowest. After standby, the screen
brightness will be recovered
• Cancel: click『Cancel』, and return to the interface before the OFF setting
Note: The equipment has a standby function only under the non-working state.
Replace Infusion Set/Infusion Container
Please replace the infusion set assembly according to the following steps:
• Close the flow rate adjuster of the infusion set assembly, open the ProMAX IV Touch Digital Infusion
Pump Door, and then remove the infusion set assembly
• According to page 14, prefill and install the new infusion set assembly
• Operate to restart infusion according to the above infusion steps if needed
Please replace the fluid/drug container according to the following steps:
• Close the flow rate adjuster of the infusion set assembly
• Remove the fluid/drug container from the infusion set assembly
• Connect the infusion set with the new fluid/drug container
• Restart infusion according to the above steps of replacing infusion set assembly
The infusion set will distort if it works for an extended period and result in inaccuracies or flow rate error,
it's suggested to replace the pump position or infusion set after working for 8 hours.