ProMAX 7350370080540 Syringe Pump User Manual

7350370080540 Syringe Pump

Product Information

The ProMAX Syringe Pump is a veterinary syringe pump designed
for professional use by trained veterinarians and maintenance
technicians. It is equipped with mechanical and touch buttons for
easy operation. The pump meets the international standard IEC/EN
60601-1 for electric devices.

Table of Contents

• Dialogue Window
• Symbols
• Other Functions
• Patient Information (optional)
• Prescription (optional)
• Calibration
• Repair
• After-Sale Service
• Appendix
• Appendix Alarm and Solution

Safety Instructions

It is important to follow these safety instructions when using
the ProMAX Syringe Pump:

• This equipment should only be operated by trained professional
  medical care personnel.

• This equipment is not suitable for blood transfusion.

• Avoid placing or using the equipment in an environment with
  flammable or explosive articles to prevent fire or explosion.

• Before starting the infusion, ensure that the inputted infusion
  parameters are in accordance with medical advice.

• Do not solely rely on the alarm system; periodically check it
  to prevent accidents.

• Securely fix the equipment on the infusion stand and ensure
  stability. Take caution when moving the stand and equipment to
  avoid dropping or knocking into surrounding objects.

Product Usage Instructions

1. Ensure that you are a trained professional medical care
   personnel.

2. Place the ProMAX Syringe Pump on a stable infusion stand.

3. Connect the necessary components and accessories provided by
   Covetrus.

4. Make sure that the environment is free from anesthetic and
   other flammable or explosive articles.

5. Verify that the inputted infusion parameters align with medical
   advice.

6. Start the infusion process.

7. Regularly monitor the equipment and check for any alarms or
   warnings.

8. Periodically check the equipment’s stability and secure it on
   the infusion stand as needed.

9. When moving the equipment or infusion stand, exercise caution
   to prevent accidents.

Note: For detailed instructions on specific functions,
calibration, repair, after-sale service, and troubleshooting, refer
to the corresponding sections in the user manual.

ProMAX Syringe Pump
User Manual
Syringe Pump for Veterinary Use

Table of Contents
Preface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 Application Scope . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 Applicable Object . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 Use Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 Paraphrase . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 Description of Revision of User Manual . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Safety Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 Safety Information & Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 Cautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3
Dialogue Window . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 Application Scope . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 Expected Purpose . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 Expected Working Environment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 Suitable object . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5 Contraindications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 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 Display Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 Title Bar . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 Typical Interface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10 Typical Interface Icon Paraphrase . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11 Rear View . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12
Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13 Unpacking and Checking . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13 Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13 Install the Covetrus® ProMAX Syringe Pump . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 13
Use Preparation & Cautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14 Use Preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14 Operation Cautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Basic Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15 Operation Flow . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15 Infusion Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15 Equipment Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15 Starting and Self- test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15 Install Syringe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15 Remove Air Bubble . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16 Change the Rate During Infusion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16 Bolus Application . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 16 Remove the Syringe . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17 Power OFF or Standby . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 17

Table of Contents
Set Infusion Parameters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18 Introduction to Infusion Parameters Setting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18 Infusion Mode Setting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18 Rate Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18 Time Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 18 Body Weight Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19 Drug Library Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19 Sequence Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19
System Setting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19 Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19 Drug Library . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19 KVO Rate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19 Bolus Rate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19 Commonly used syringe brand . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19 DPS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19 Occlusion Pressure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 19 Pressure Unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20 Pump Idle Alert . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20 Finish Pre- Alarm . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 20 Micro Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21 Reset Total Volume . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21 General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21 Date & Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21 Brightness . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21 Sound . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21 Screen Lock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21 Night Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 Battery Capacity Display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 Nurse Call (optional) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 Nurse Call Alarm Level (optional) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 Net Work (optional) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 Language . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 Factory Default . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 Version . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 Serial Number (SN) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 Software Version . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22 Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Other Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23 Patient Information (optional) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23 Prescription (optional) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
History Entries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23 Last Therapies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23 Anti-bolus . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Alarm Prompt and Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23 Introduction to Alarm Level . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23 Multilevel Alarm Rules . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24 Alarm Treatment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24 Fault Analysis and Solution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24

Table of Contents
Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24 Cleaning, Disinfecting, and Sterilizing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24 Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24 Disinfecting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
Periodical Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25 Check the Appearance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25 Performance Check . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25 Maintenance Plan . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26 Repair . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Normal Repair Process . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26 Maintenance for Long-Term Storage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26 Equipment Components/Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26 Production Date . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26 Recycling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27 Check the Battery Performance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27 Replacing the Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
After-Sale Service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Appendix . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28 Appendix Alarm and Solution. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 28

Preface
Application Scope
Applicable to the Covetrus® ProMAX Syringe Pump. This user manual describes the product’s most complete configuration. For more detailed information, please contact Covetrus.
Applicable Object
It applies to professionally trained veterinarians and maintenance technicians of this equipment.
Use Instructions
The Covetrus ProMax Syringe Pump 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. 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
   Triumph Medical 3. All components and accessories, as well as consumables for repair, are provided by Covetrus 4. Relevant electric devices meet the international standard IEC/EN 60601-1 and this user manual
   Paraphrase
   Mechanical button Touch button ( ) Information – Inapplicable Accordant Operation steps
   Bolus: Infuse large volume of liquid in a short time. KVO: Keep vein open and prevent blood back to the syringe extension line. Anti-bolus: Motor automatically reverses while the syringe extension line and needle have high pressure. IrDA: Infrared Communication Warning /Attention: can possibly cause physical injury or death if the cautions covered in the Warning are not obeyed. Caution: can possibly cause physical injury if the cautions are not obeyed. Note: if user fails to follow the supplementary or prompt information on the operating instructions, it may cause physical damage to the equipment if it is not obeyed. Accessories: the optional components which are necessary and (or) suitable for use with the equipment to achieve the expected purpose, provide convenience for attaining the expected purpose, improve the expected purpose, or increase the additional functions of the equipment.
   Description of Revision of User Manual
   The Covetrus® ProMAX Syringe Pump User Manual will be revised subject to product improvement, laws updating, or instructions improvement based on the preconditions of meeting related laws and regulations. All revisions will be documented in the new version.
   1

Safety Instructions
Safety Information and 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 Covetrus®. 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.

This equipment must be operated by trained professional medical care personnel.

This equipment does not apply to blood transfusion.

It is not allowed to place and use the equipment in an environment with anesthetic and other inflammable or explosive articles to avoid fire or explosion.

It is not allowed to store or use the equipment in an environment with active chemical gas (including gas for disinfecting) and a moist environment since it may influence the inside components of the Covetrus® ProMAX Syringe Pump and may possibly cause performance drop or damage the inside components.

The operator shall guarantee that the inputted infusion parameters of this equipment are the same as the medical advice before starting the infusion.

Please do not depend only on the alarm system during use; please periodically check it to avoid an accident.

Tightly fix this equipment on the infusion stand and ensure its stability of the infusion stand. Be careful when moving the infusion stand and the equipment to avoid the equipment dropping and the infusion stand falling or knocking the surrounding objects.

If the syringe extension line is twisted, the filter or needle is obstructed, or there is blood in the needle which may obstruct the syringe, the pressure in the syringe will rise. Removing such occlusion may cause a “bolus infusion” (temporary excess infusion) to the patient. The correct method is to tightly hold or clamp the extension line near the puncturing position, then loosen the syringe, solve the reason for occlusion, and restart the infusion. If the infusion is restarted when the occlusion reason exists, then it may cause a persistent occlusion alarm. This will cause the pressure in the syringe to rise and may break or cut OFF the connection or hurt the patient.

This equipment has an occlusion detection function for detecting and alarming when the syringe needle deviates from the position in the vein or the needle is not correctly punctured in the vein. However, it only alarms when the occlusion pressure has reached a certain numerical value. At this point, the puncturing site may have become reddish, swelling, or bleeding. Additionally, it is possible that the device doesn’t alarm for an extended period if the actual occlusion pressure is lower than the alarm threshold value; therefore, please periodically check the puncturing site. If there’s any abnormal phenomenon for the puncturing site, please take suitable measures, such as puncturing again.

Only those sterile hypodermic syringes for single use and other medical components that meet the local laws and regulations and the requirements covered in this user manual can be adopted. It is suggested to adopt the syringe with the same brand as defaulted in this equipment. Infusion accuracy is not ensured if an unsuitable syringe is adopted. Please use the syringe and the extension line with luer locks, or the extension line might pop off, causing injury to the patient.

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.

To avoid the risk of electric shock, this equipment must only be connected to a supply main with protective ground earth.

2

Cautions
Before its first use after purchase, or if the equipment is not used for an extended period, please charge the equipment with an AC Power Supply. If not fully charged, the equipment may not work with the built-in battery power supply under a power failure.
This equipment can’t be used in locations with radiological installation, magnetic resonance equipment, or places with high-pressure oxygen therapy.
Under general conditions, please use an AC power supply as much as possible since it can prolong the service life of the battery to a certain degree. When using an 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 AC 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 to 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 keep the equipment away from the AC Power socket for a certain distance to avoid fluid/drug splashing or dropping in the socket. Otherwise, it may possibly cause a short circuit.
Please use the fluid/drug after it has reached or nearly reached room temperature. When the fluid/drug is used at a low temperature, the air which is dissolved in the fluid/drug may cause more air bubbles.
It is not allowed to press and operate the button with a sharp object (such as a pencil tip and nail). Otherwise, it may possibly cause early damage to the button or surface film.
Under the condition of low flow rate infusion, please pay special attention to an occlusion. The lower the infusion flow rate, the longer the time of detecting occlusion, which may cause a long-time infusion stop 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.
Dialogue Windows
Dialogue window mainly includes operation select, operation confirm, and information.
3

Symbols
Not all of the below symbols exist on the equipment you have purchased.

Marks

Description

Marks

Description

Lot Number

Class I Equipment

Attention, consult accompanying documents
Non-Ionizing Radiation
Environment-friendly use period (20 years)

Alternating Current Input and output Handle with care

Date of Manufacture
Defibrillation Proof Type CF Applied Part

SN

Serial Number

Unlock

IP34

Manufacturer
Please refer to the User Manual
Ingress Protection (prevent solid objects larger than 2.5 mm in diameter and water intrusion from splashing in all directions)
Lock

4

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.
Suitable object Companion animals

Contraindications
No

Working Principle
It is controlled to move into a linear motion from a microcontroller-based system that drives a step motor, allowing a wide range of pumping rates configured to the inside diameter of the loaded syringe. The syringe plunger is driven from a lead screw and drive-nut mechanism, infusing the drugs into the patient.

Structure and Performance
Structure and Performance The Covetrus® ProMAX Syringe Pump comprises the main unit and built-in battery. This equipment provides several infusion modes, such as rate mode, time mode, body weight mode, drug library mode, and sequence mode. It also has functions such as history records, drug library, Anti-bolus, alarm, etc.

Product Specification

Safety Classification

Electric Protection Type

Class I

Electric Protection Level Ingress Protection
Working mode Classification

Defibrillation proof type CF applied part IP34 (Prevent solid objects larger than 2.5 mm in diameter and water intrusion from splashing in all directions)
Continuous
Portable equipment, non-portable syringe pump

Specification Parameters
Compatible Syringes System Accuracy Infusion Rate

3 ml, 5 ml, 10 ml, 20 ml, 30 ml, 50/60 ml
1ml/h, ±2% 1ml/h, ±5%
Syringe size 3 ml: (0.1-100) ml/h Syringe size 5 ml: (0.1-150) ml/h Syringe size 10 ml: (0.1-300) ml/h Syringe size 20 ml: (0.1-600) ml/h Syringe size 30 ml: (0.1-900) ml/h Syringe size 50 ml: (0.1-1500) ml/h

5

Specification Parameters (continued)

Bolus Rate

Syringe size 3 ml: (0.1-100) ml/h Syringe size 5 ml: (0.1-150) ml/h Syringe size 10 ml: (0.1-300) ml/h Syringe size 20 ml: (0.1-600) ml/h Syringe size 30 ml: (0.1-900) ml/h Syringe size 50 ml: (0.1-1500) ml/h

Bolus preset value

Min: 0.1 ml Max: max rate of accordingly loaded syringe size

KVO Rate

0-5.00 ml/h

Micro Mode Setting Range

Syringe size 3 ml: (100) ml/h Syringe size 5 ml: (100-150) ml/h Syringe size 10 ml: (100-300) ml/h Syringe size 20 ml: (100-600) ml/h Syringe size 30 ml: (100-900) ml/h Syringe size 50 ml: (100-1500) ml/h

Minimum Flow Rate Increment

0.01 ml/hour

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 Weight

242.5 (w) x 111 (d) x 126.5 (h) mm 1.7 kg, 3.75 lbs

Power Supply
AC Power Supply Input Power DC Power Supply Battery Specifications

100-240V 50/60Hz
50VA
DC 12V
Specification: 7.4V 2500mAh Charging time: single battery less than 2.5 hours, two batteries less than 5 hours (under OFF status) Working time: single battery over 5.5 hours, two batteries over 11 hours (after completely charging battery/batteries, when the environment temperature is 25°C or 77° F and flow rate is 5 ml/h constantly)

6

Alarm
Alarm Signal Sound Pressure Level
Alarm Information

When the sound is set at lowest level, alarm signal sound pressure level 50dB(A) When the sound is set at highest level, alarm signal sound pressure level 80dB(A)
VTBI near end, Syringe near empty, VTBI infused, Syringe empty, Occlusion (Pressure high), Battery nearly empty, Battery empty, no battery inserted, No power supply, check syringe, Pump Idle Alarm, Standby time expired, KVO finished

Environment
Non-AP/APG type equipment Operating
Transport and Storage

Do not use it in an environment with inflammable anesthetic gas mixed with air, and inflammable anesthetic gas mixed with oxygen or nitrous oxide
1. Temperature: 5­40°C, 41­104°F 2. Humidity: 15-95%, Non-Condensable 3. Atmospheric Pressure: 57-106kPa
1. Temperature: -20­55°C, -4­131°F 2. Humidity: 10-95%, Non-Condensable 3. Atmospheric Pressure: 50-106 kPa

Safety Standard
Main Safety Standards

IEC 60601-1 : 2005+A1 : 2012 Medical Electrical Equipment ­ Part 1 : General Requirements for Basic Safety and Essential Performance
IEC60601-2-24 : 2012 Medical Electrical Equipment ­ Part 2-24 : Requirements for the Safety of Syringe Pumps and Controllers
IEC60601-1-82006+A12012 Medical Electrical Equipment ­ Part 1-8 : General Requirements for Basic Safety and Essential Performance ­ Collateral Standard: General Requirements, Tests, and Guidance for Alarm Systems in Medical Electrical Equipment and Medical Electrical Systems
EN60601-1-2 : 2007+AC : 2010 Medical Electrical Equipment ­ Part 1-2 : General Requirements for Basic Safety and Essential Performance ­ Collateral Standard: Electromagnetic Compatibility – Requirements and Tests

7

Appearance Front View

Part Number

Name Handle

Slider Box

Pressure Sensor

Syringe Clip

Leadscrew

Syringe Fixture Lever

Control the Covetrus® ProMAX Syringe Pump push-pull sliding box and clip
Detect the pressure of the syringe Clamp the syringe plunger
Pull forward, turn 90° right or left, and install the syringe into the slot. Keep the extension line straight and neat

8

Operation Panel

Part Number

Name Touch Screen
Power

AC Indicate Light
Alarm Indicator Light
Running Lights Start/Stop Bolus/Purge Home

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. When connected to the AC power supply, the AC indicator light is on. While pump alarms, the indicator light glitter, different level, different frequencies and color, for more information, please refer to page 21
Enter system home page
9

Display Screen
The display screen interface layout composes of a title bar and typical interface

Title Bar
The title bar displays real-time information and is not touchable, and the left upper corner displays the name of the current editing parameter.

Icon

Paraphrase
Syringe Apparatus Indication Icon
Lock Screen Indication Icon
WIFI Indication Icon
Battery Charging Indication Icon
Battery Status Indication Icon

Description
Syringe apparatus indication icon
Unlock state icon is
Indicates WIFI connection state
Display the current battery charging state
Battery life percentage is displayed on the left side of the icon Battery icon may show the following states:

Typical Interface
During pre-infusion and infusion, the standard interface will display the following: main interface, working interface, alarm interface, prompt interface, control panel, parameters setting, input method, standby interface, etc.

10

Typical Interface Icon Paraphrase

Icon

Paraphrase

Start

Stop
Bolus/ Purge

Home

Description
Click this icon to start infusion
Click this icon to stop infusion
1. During infusion, it is aBolusfunction­click it to start fast infusion 2. Before infusion starts, it is aPurgefunction­click it to exhaust air
from the syringe
Click this icon, return to the main interface

Input Method Interface The input method interface comprises the title bar, input box, and editing box.

· Title bar: displays the name of the current editing parameter. · Input box: real-time display of the input content. · Editing box: It composes of the main button area and function button area.
The main button area comprises the numerical value, letters, and icons. Click it continuously to change the sequence.

The function button area composes of a clear button, backspace button,

,

,

and Shift.

Icon

Paraphrase
Backspace Button Shift Button
Cancel Button OK Button

Description
Click it to backspace and delete Click it to switch the capital and lowercase English letters Click it to cancel editing and exit Click it to save editing and exit

11

Rear View

Part Number

Name

USB Port

Port only for software upgrade

DC Input Port

External 12V DC Power Supply

Handle

A/C Adapter Port

External 100-240V 50/60Hz AC Power Supply

Pole Clamp

Using for fixing the equipment on the infusion stand

Loudspeaker

IrDA

Using for communicating with infusion docking station (Optional)

Latch for stackable function

Slider Box

12

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.
Please put the packing materials out of reach of children. Please obey local laws and regulations when disposing of items.
Installation
· The Covetrus® ProMAX Syringe Pump shall be installed per the instructions of this user manual · All devices that connect with this equipment must pass the designated IEC standards (for example, IEC60950
information technology equipment safety and IEC60601-1 medical electric device safety) certification, and all devices must be connected according to the correct version of the IEC60601-1-1 system. The technician who connects to additional devices with the equipment interface is responsible for meeting the IEC60601-1-1 standard. Please contac tCovetrus® for any questions. · When connecting this equipment with other electric devices to form a combination for special circumstances, 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 aligned guidelines from this manual
Install the Covetrus® ProMAX Syringe 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 Covetrus® ProMAX Syringe
Pump, and tighten the Pole Clamp to fix the ProMAX Syringe Pump on the infusion stand (as shown in the drawing below). Hold the ProMAX Syringe Pump 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
13

Use Preparation & Cautions Use Preparation
If the Covetrus® ProMAX Syringe Pump is new, reused after storing for an extended period, or reused after repair, please check and ensure the following before use: · The equipment’s appearance is clean and in good condition without cracks and leakage · The moving components are smooth and working. The buttons are working · 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 · In case 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 equipment shall be put at a position less than 0.65 m (both up and down) to the heart of the patient · The parameters can only be set or changed by trained and professional personnel · Avoid using faulty equipment to avoid medical negligence, which may hurt the health and even the life
of the patient · 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
14

Basic Operation
Operation Flow
· Mount the Covetrus® ProMAX Syringe Pump on the IV stand: refer to page 13 · Power on: press two seconds, power on equipment; refer to below · Install syringe: refer to below · Confirm syringe brand and size: Select syringe brand · Remove an air bubble in the line: refer to page 16 · Select infusion mode: Select infusion modes according to requirement · Set infusion parameters: set infusion parameters according to requirement · Connect infusion line with the animal · Start infusion: press , start infusion · Finish infusion: refer to page 17 · Remove syringe: refer to page 17 · Power off or Standby: refer to page 17
Infusion Operation
Equipment Installation Mount the device on the infusion stand according to page 13, 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 two seconds, then power on 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, Covetrus® ProMAX Syringe Pump enters into rate mode interface.
If the self-test fails, the Covetrus ProMAX Syringe Pump cannot be operated properly or is damaged, it cannot be used for animal infusion; please contact Covetrus®.
Install Syringe · Hold the clutch (Handle) and pull the slider (arm) to the right side · Pull the Syringe Fixture Lever (barrel clamp), and turn 90° right or left · Insert the syringe flange into the slot, turn the Syringe Fixture Lever 90° spring back to tighten the
syringe, and confirm the correct syringe brand/size · Hold the clutch (Handle) and push leftward–release after it touches the plunger firmly · Put the extension line of the syringe into the extension line hook · ClickSettingCommonly used Syringe brandt o choose syringe brand if not selected
· Only use syringe brands defaulted in this syringe pump · Ensure syringe brand and size on the display screen are in accordant with the one in use · Contact Covetrus® if you are unsure of the correct syringe Manufacturer and size­selecting the
wrong Manufacturer or size can compromise accuracy and possibly cause injury to the animal.
· Check to ensure no air bubbles are in the syringe · Make sure the syringe is correctly installed. Otherwise, accuracy will not be assured and may harm
the animal
15

Set Infusion Parameters Refer to page 18
Remove Air bubble Under the parameters setting interface, Press theBolusbutton and hold, or touch the purge icon on the product panel, to eliminate the air bubbles in the line. The purge total volume is not calculated in the Total Volume Infused.
· Before purging the air, double-check to confirm the infusion line is not connected with the animal · Purge rate is the max rate of the syringe size. The purge will automatically stop when the volume is
5 ml

Start Infusion

Connect syringe extension line to the patient, confirm infusion parameters, PressStartbutton ,

click yes

in the pop-up prompt interface, and start infusion.

Change the Rate During Infusion
Under the running interface, click the rate number in the Touch Screen orStop , enter parameters setting interface, and reset the target infusion rate.
Note: Only rate mode, time mode, and body weight mode support online rate modification
function during infusion without pressingStop .
Bolus Application
During operation, the bolus functions have two operation modes: Manual bolus and Automatic bolus.
· Manual bolus: press and hold the Bolus button on the product panel, and the pump will work at the max flow rate of the current syringe size or set the max bolus rate under the setting interface. (For syringe flow rate range, please check in the setting interface and refer to page 5, release the button, and Covetrus® ProMAX Syringe Pump will return to the previous infusion rate
· Automatic bolus: Under the running interface, click theBolus on the Touch Screen, set two parameters among bolus infusion volume, rate, and time, and clickStart; it will beep at every 1 ml infused. After the bolus infusion is finished, the equipment will return to the previous infusion rate

16

Infusion Completion When the remaining infusion time is near the preset volume to be infused completion time, Covetrus® ProMAX Syringe Pump will alarm. If the user ignores it, the system will keep alarming until complete. For more information, please refer to page 20. 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 30 minutes. After reaching that time, it will activate the KVO completion alarm and stop infusion. Please refer to page 19 for setting the KVO rate. Stop Infusion During infusion or after infusion, click and infusion will stop. It will return to the parameter setting interface and display Total Volume Infused and adjustable parameters. Remove the Syringe Disconnect the extension line from the patient, then remove the syringe. To replace the syringe, please follow the steps from page 15. Power OFF or Standby Method 1: hold the PowerButton till the screen and equipment are OFF. Method 2: Press PowerButton to enter into the OFF interface. · Turn OFF the equipment: clickPower officon, the equipment is turned OFF · Standby: clickStandbyicon 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 brightness will be recovered · Cancel: clickCancel, and return to the interface before the OFF setting
Note: The equipment has a standby function only under the non-working state.
17

Set Infusion Parameters
Introduction to Infusion Parameters Setting
· The drug information can only be displayed in the infusion running interface when the drug library is active ClickSettingsi con in the main interface to enter the sub-menu, find theDrug Library menu item, click to enter, then set the ON/OFF state of the drug library and select drug. Please refer to this User Manual, page 23, for details
· For both the rate set in the infusion parameter and the rate calculated by the system, the range is the system default flow rate of the current working syringe specification
· If VTBI (Volume to be infused) is set, the pump will infuse all the fluid/drug in the syringe

Infusion Parameters Setting Range

Infusion Parameter
VTBI

Parameter Range
0-9999.99 ml, minimum step is 0.01 ml

Rate

(0.1-100) ml/h for 3 ml syringes (0.1-150) ml/h for 5 ml syringes (0.1-300) ml/h for 10 ml syringes (0.1-600) ml/h for 20 ml syringes (0.1-900) ml/h for 30 ml syringes (0.1-1500) ml/h for 50 ml syringes

Time

1 minute – 99 hours 59 minutes

Weight (Body Weight)

0.1-300 kg

Active Agent (Drug Mass)

0.01-99999.99

Concentration Unit

ng, ug, mg, g, U, kU, IU, IE, mmol, mol, kcal

Volume (Fluid Amount)

0.01-9999.99 ml

Dose Rate

0.1-9999.99

Dose Rate Unit

Unit(/kg)/minute, Unit(/kg)/hour, the unit is Concentration Unit

Infusion Mode Setting
After starting the Covetrus® ProMAX Syringe Pump and self-test, the equipment automatically enters into the rate mode parameters setting interface. To select other modes, clickMenuicon to enter into the main interface, clickModesicon to enter into the mode selection menu interface, and select preset infusion mode.
Rate Mode This mode allows the user to set three parameters: Rate, VTBI (Volume to be infused), and Time. Set any two of the three parameters, and the system will automatically calculate the third parameter. If the VTBI is 0, the Covetrus® ProMAX Syringe Pump works at the set rate until it stops with an alarm.
Time Mode In this mode, it allows the user to set VTBI (Volume to be infused) and Time, and the system will automatically calculate the speed, speed = Volume (ml)/time (minute).
18

Body Weight Mode Under this mode, set the Weight (body weight), Conc. Unit (concentration unit), Active Agent (drug mass), Volume (fluid volume), Dose rate, Dose unit, VTBI. The system will automatically calculate the flow rate from the specified dose rate (ug/kg/minute, mg/kg/minute, ug/kg/hour, mg/kg/hour, etc.) according to the related formula {dose rate × weight}/ {Active agent (drug mass)/Volume (fluid volume)}, and automatically calculate the time according to (VTBI) / (flow rate).
Note: VTBI must be greater than the Loading dose VTBI; otherwise, the excess part can’t be set when the setting exceeds the limit.
Drug Library Mode Under this mode, Select Drug, set the Weight (Body Weight), Conc. Unit (Concentration Unit), Dose, and VTBI (Volume to be infused. The speed will automatically be calculated according to the parameters. Drug Library Editable (see below in System Settings). Sequence Mode Sequence mode is to infuse according to a set sequence after programming the rate and time of different sets of sequences. Up to 10 different sequence groups can be programmed.
System Setting
Settings
ClickSettingsicon in the main interface to enter into the parameters setting interface. Drug Library Click on the preset drug name, and the selected drug will be reflected in the infusion mode parameters. This feature can be turned ON and OFF. Covetrus® ProMAX Syringe Pump supports 30 drugs without upper and lower limits. KVO Rate ClickKVO rate, input the numerical value, after confirming, clickOK. Please refer to page 6 for the adjustable KVO range. Bolus Rate Set the default Bolus rate. Please refer to page 6 for the range of bolus rate. Commonly used syringe brands Syringe brands are built in without the need for users to self-calibrate. If there are any questions about compatibility, please contact Covetrus®.
The syringe of a different brand may cause flow rate deviation. When using, please confirm if the displayed information in the interface corresponds with the actual syringe brand/size in use.
DPS DPS, or dynamic pressure sensing, can be carried out after opening, and an alarm can be triggered when the pressure rises or suddenly falls. This function is optional. Occlusion Pressure ClickOcclusion pressureto enter into the occlusion level setting interface, move the long box to the preset level, and after confirming, clickOK. The higher the level, the higher the occlusion level, so it is suggested to select suitable occlusion pressure according to the actual requirement.
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· When adopting a fluid/drug of high viscosity and the occlusion pressure is set at a low level, the system may report an occlusion alarm even when the line is not obstructed
· Under this condition, please carefully observe the pressure indication icon in the display screen and infusion line and raise the occlusion pressure if needed
· When the occlusion pressure is set to high grade, the high pressure inside the pipeline is likely to pop out the extension line connected to the syringe. Please confirm that the extension line is securely attached to the syringe
· When the occlusion pressure is set at a high level, it may cause the patient to be uncomfortable. After raising the occlusion pressure, please carefully observe the condition of the patient and immediately take measures if there’s any abnormality
· Under the equipment fault state, the max pressure generated by the infusion line is 300 kPa
· Under single fault state, the max infusion volume is 2ml

Relation of Occlusion Level and Pressure

Applicable Model: Covetrus® ProMAX IV Syringe Pump Occlusion Pressure Level: 4 levels

Level

Pressure Intensity (mmHg)

Level

Pressure Intensity (mmHg)

Level

Pressure Intensity (mmHg)

Level

Pressure Intensity (mmHg)

1

50

2

300

3

600

4

900

Pressure Unit Click Pressure unitto enter into the pressure unit select setting interface; four units are available: mmHg, kPa, bar, and PSI. Click the preset unit option.
Note: Please carefully confirm when changing the current pressure unit.

Unit Mark
kPa PSI Bar

Unit Conversion
1 kPa=7.5 mmHg=0.145 psi=0.01 bar 1psi=51.713 mmHg=6.895 kPa=0.069 bar 1bar=787.5 mmHg=15.225 psi=105 kPa

Pump Idle Alert
ClickPump Idle Alertto enter the time for the reminder alarm setting interface, and click the preset time option to set the reminder alarm time.
Pump Idle Alert refers to the alarm that will be prompted if there is no key operation within the preset idle alert time when the device is in the non- infusion and non-alarm state. Pump idle alert time is settable to 2 minutes, 5 minutes, 10 minutes, 15 minutes, 20 minutes, and 30 minutes.
Finish Pre-Alarm
Time for pre-alarm refers to activating near completion alarm when the fluid/drug infused volume nearly reaches the preset value.
Click Finish Pre-Alarmto enter the time for the pre-alarm setting interface, click the preset time option to set the finish pre-alarm time.

20

Micro Mode
Click Micro modeto enter into the micro mode setting interface. ON/OFF is optional in this function Optional. Under the ON mode, set the rate limit, then the infusion rate under any infusion mode is not allowed to exceed this limit.

Syringe Size

Max Rate Range

3 ml 5 ml

100 ml/h 100-150 ml/h

10 ml 20 ml 30 ml 50 ml

100-300 ml/h 100-600 ml/h 100-900 ml/h 100-1500 ml/h

Reset Total Volume
ClickReset total volume, the interface displays the operation confirming prompt box, clickYes to confirm reset; otherwise, please clickNo
General
In the main interface, clickGeneralto enter into the General Covetrus® ProMAX Syringe Pump setting interface.
Date & Time
ClickDate & Timeto enter into the date and time setting interface. It allows the user to set the date, time, and format in this interface.
When setting the date and time, directly input the numerical value in the input method interface. For example, for “2023-04-24”, input “20230424”; to preset the time “12: 34”, input “1234”. The time is in 24-hour or 12-hour format, and the date is in British, American, or Chinese type. Please set according to the requirement.
Brightness
ClickBrightnessto enter into the display brightness setting interface. The brightness has 10 levels. The Covetrus® ProMAX Syringe Pump automatically adjusts brightness if the external power supply is unavailable. When there is no external power supply, and a battery supplies the power, if it is not operated within 3 minutes, the system will automatically adjust the brightness to the lowest level when it is touched, or the user clicks a button, or when there’s an alarm, it will automatically recover the brightness.
Sound
ClickSound to enter into the sound parameters setting interface. The volume has 10 levels. The lowest volume is 50dB, and the highest is 80 dB. Move the long box to the preset value. After confirming, clickOK
Screen Lock
ClickScreen Lockto enter into the automatic lock screen setting interface, and select ON or OFF. Automatic lock screen time can be set at 15 seconds, 30 seconds, 1 minute, 2 minutes, 5 minutes, 10 minutes, 30 minutes, etc., which means that the Covetrus ProMAX Syringe Pump will automatically lock the screen if it is not touched, or the button is pressed within corresponding time after starting.
Unlock: directly clickCancelin the lock screen interface.
Note: The Covetrus ProMAX Syringe Pump will automatically unlock if there’s a high-level alarm.

21

Night Mode
ClickNight Mode to enter into night mode switch setting interface to set the start and end time of the night mode and the night brightness. At night, the system automatically adjusts the brightness to the user-defined value.

Battery capacity display
Turn it on to show the battery life in the upper right corner of the screen and turn it OFF to show the percentage of remaining battery life.

Nurse Call (optional) *Additional software required. ClickNurse callto select function ON and OFF (optional).

Note: The nurse call function must be used with a special cable. The user shall not only depend on the nurse call function as the main alarm notice mode and shall identify according to the Covetrus® ProMAX Syringe Pump alarm and the patient state.

Nurse call alarm level (optional)
*Additional software required. Selecting the nurse call alarm level, when the alarm level reaches the chosen level, the nurse call alarm is conducted.

Network (optional)

*Additional software required. The Covetrus ProMAX Syringe Pump supports wireless or wired

connectivity when equipped with a wireless module and connected to the internet through WIFI;

the ProMax Syringe Pump screen displays

icon.

ClickNetworkin main interface to set the response.

Note: This function shall be set by a professional equipment maintenance technician.
After activating the connectivity function, the equipment can periodically transmit the equipment data, and the data is only for displaying and doesn’t make suggestions of a medical or therapeutic nature.

The connectivity channel supports WLAN and serial port modes. Please select according to the actual requirement.
When WIFI function is in use, turn on the WLAN switch of the equipment, set the name and password of the access point, and configure the TCP/IP parameters.

Note: The wireless access must be set up by a professional technician recognized by Covetrus. The transmitted data of this equipment doesn’t make suggestions of a medical or therapeutic nature, and this data shall not be used for calculating the therapeutic schedule. When data is used by external equipment or software, it is only for displaying, and shall not be used for alarming or calculating.

System

ClickSystemunder the menu interface, enter the system information setting interface.

Language The Covetrus® ProMAX Syringe Pump supports simplified Chinese, English, and other languages.

Factory Default ClickFactory defaultto clear the user-defined option, and this function is open to the user.

Version Shows current software version.
Serial Number (SN) – Check the serial number of the Covetrus® ProMAX Syringe Pump. The user cannot modify the serial number. Software version – Check the software version in this interface.

Maintenance This interface is used by Triumph Medical to maintain and calibrate equipment.

22

Other Functions
Patient Information System (optional)
Patient Information (optional)
Additional software required. ClickPatientto enter into the patient information setting interface and set bed number, MRN, name, gender, age, body weight, and height.
Prescription (optional) Additional software required. ClickPatientto enter into the patient information setting interface and enter the end of the submenu, find menu item Prescriptionand enter to set the medical advice ID, medical advice information, start time, and state.
History entries
Click Recordsin the main interface to enter the sub-menu and click the “History entries” menu item into history records query interface. The Covetrus® ProMAX Syringe Pump saves over 5000 history records and can display the event name, event date, and time (permanent preservation). When it is full, the new records will replace the old records with the first in, first out principle.

Alarm Prompt and Troubleshooting
Introduction to Alarm Level
During infusion preparation and infusion, the Covetrus® ProMAX Syringe Pump will alarm when reaching or exceeding the set alarm threshold value and prompt with sound, light, and text. According to the importance of alarm information and emergency and safety, the alarm is divided into high, middle, and low levels. Please refer to the table below for details:

Alarm Level
High alarm Middle alarm Low alarm

Sound Signal Interval
10s 15s 20s

Light color/flash frequency
Red indicator flashes /2.0±0.6Hz Yellow indicator flashes / 0.6±0.2Hz Yellow indicator lights on

If there’s an alarm, the system will display the alarm interface. If the alarm level is high, click OK, stop the alarm, and exit the alarm interface. If the alarm level is middle or low, click OK, the sound signal will stop, and exit the alarm interface.
ClickMuteto mute. If the alarm is not eliminated, the alarm sound will be sent out 2min later.

Some alarm threshold values of the Covetrus® ProMAX Syringe Pump can be set by the user, for example: Occlusion pressure, pump idle alarm, VTBI infused pre- alarm, alarm sound volume, and so on, the user shall confirm the parameters when setting the alarm threshold value. Otherwise, it may influence the alarm function or infusion safety.

23

Multilevel Alarm Rules
When there’re several alarms, the system will alarm according to the following rules:

Multilevel Alarm

Rules

Several alarms of different levels generate simultaneously
Several alarms of same level generate simultaneously

Display the alarms of highest level with sound, light, and text, report middle alarm after eliminating all alarms of the highest level
Alarms circularly by turns, the time interval is 1s

When alarming, the corresponding alarm information will display on the title of the screen. Refer to Appendix A for more information

Alarm Treatment

When there’s an alarm, please check the conditions of the animal, remove the reason of the alarm, and then continue working.
Please refer to Appendix for the alarm solution.
Fault Analysis and Solution
When there’s a fault, the Covetrus® ProMAX Syringe Pump screen will display the fault alarm information; this item is an alarm of high level. Please eliminate the fault alarm according to the prompt. If it can’t be eliminated, please stop the Covetrus® ProMAX Syringe Pump, and contact Triumph Medical to repair and test it, and do not put it into operation before it has passed the inspection. Otherwise, it may possibly cause unpredictable harm if it works with a fault. If the Covetrus® ProMAX Syringe Pump is on fire/burns for unknown reasons or has other abnormal conditions, the user shall immediately cut off power supply and contact Triumph Medical.

Maintenance Cleaning, Disinfecting, and Sterilizing
· Please cut OFF the Power Supply and unplug the DC /AC Power Cord before cleaning the equipment · During cleaning and disinfecting, please keep the equipment horizontal and upward to protect the
equipment and accessories from fluids

Cleaning
· The daily maintenance is mainly to clean the shell and pump body · Fluid/drug may inevitably flow in the equipment during infusion · Some fluid drugs may corrode Covetrus ProMAX Syringe Pump Slider and cause a working fault · After infusion, please timely clean the equipment, wipe it with moist and clean soft fabric, and then
naturally dry it
· When cleaning the Covetrus ProMAX Syringe Pump Slider interface, please wipe it with dry and soft fabric, and confirm the interface is dry before using
· Please do not soak the equipment in water. Although the Covetrus ProMAX Syringe Pump Slider has a certain waterproof function, when fluid splashes on the equipment, please check if it works normally and perform an insulation and electric leakage test if needed

24

Disinfecting
· Disinfecting may cause harm to a certain degree; it is suggested to disinfect the equipment only if needed Please disinfect the equipment with a common disinfecting agent, such as 50% sodium hypochlorite, cidex 2% glutaraldehyde + activating agent, 70% ethanol, 70% isopropyl alcohol, etc. Please follow the instructions of the disinfecting agent
· After disinfecting, wet the soft fabric with warm water, dry the fabric, and then wipe the equipment · Do not sterilize the equipment with a high-pressure steam sterilizer or dry the equipment with a dryer
or similar product
Please do not adopt Cidex OPA ortho phthalaldehyde, methyl ethyl ketone, or similar solvent. Otherwise, it may corrode the equipment.

Periodical Maintenance
Notes: · The user should set up a complete maintenance plan. Otherwise, it may possibly cause the
equipment to malfunction or fault · To ensure the safe use and prolong the service life of the equipment, it is suggested to periodically
maintain and check it once every 12 months · Some items shall be maintained by the user, and some items shall be maintained by Triumph
Medical · Please contact Covetrus® if the equipment is found defective
Appearance Check · The appearance of equipment shall be clean and in good condition without cracks and water leakage · The buttons are depress correctly and produce the correct function when pressed; the sensitivity
of the Touch Screen is normal · The Covetrus® ProMAX Syringe Pump Slider allows for correct movement, and the Pole Clamp is
intact and without damage · The power cord is in good condition and can be installed tightly · After connecting with the external power supply, the AC indicator light turns on · Use only the accessories designated by Covetrus · The environment the Covetrus® ProMAX Syringe Pump Slider will be used in meets the requirements
of this user manual

Performance Check · Self-test and infusion functions work · Alarm function works · Battery performance
Maintenance Plan The following check/maintenance items must be performed by a professional technician recognized by our company. If the following maintenance is necessary, please contact our company. Please clean and disinfect the equipment before testing or maintaining.

Maintenance Items
Safety check according to IEC60601-1
Preventive system maintenance items (pressure calibrate, sensor calibrate)
Infusion accuracy

Cycle
Once every 2 years, please check after replacing the printed circuit board assembly or if the equipment is dropped or knocked.
Once every 1 year, when the occlusion alarm, or infusion accuracy is doubted to be abnormal
Using the equipment for the first time, using a new syringe brand for the first time, reusing the equipment after not being used for a long time

25

Calibration
Calibration is performed by Triumph Medical.
Repair
Normal Repair Process Please contact Covetrus® to repair if there’s any fault. Do not disassemble and repair the equipment. Maintenance for Long Term Storage If the equipment won’t be used for an extended period, please take out the battery, and pack it with the equipment. Store it in a cool and dry place without direct sunlight. The following operations are necessary for using it again: · Verify the flow rate accuracy to avoid unconformity between the syringe apparatus parameters in the
equipment and the actual parameters after it hasn’t been used for an extended period or caused by other reasons: otherwise, it may cause an infusion error, influence the therapeutic effects and even cause medical negligence · Perform occlusion alarm test · Test the battery discharging and charging duration to confirm that the battery is also usable
Equipment Components/Accessories
Only components and accessories designated by Covetrus® or Triumph Medical shall be adopted. Otherwise, it may damage the equipment or decrease the equipment’s performance.

Name
Pole Clamp Power Cord

Part Number
TRI-UPC-23 TRI-RTPC-23

Production Date
Please refer to the label of the product.
Recycling
The normal service life of this equipment is 10 years and depends on the use frequency and maintenance. · The obsolete equipment may be returned to Covetrus® or Triumph Medical · The used lithium-ion polymer battery has the same treatment method or according to
applicable laws and regulations

26

Battery
This equipment has a charging lithium-ion polymer battery to ensure normal infusion when the equipment is moved, or the external power supply is cut OFF. When connecting an external power supply, no matter whether the equipment is started or not, it can charge the battery. When charging, the equipment screen displays the battery charging indication icon . If only a built-in battery is adopted for supplying power, and when the remaining battery is less than 20%, please connect the equipment to an external power supply to charge the battery.
Only the battery designated by Covetrus® or Triumph Medical shall be adopted.
Check Battery Performance
The built-in battery performance may drop according to the use of the Covetrus ProMAX Syringe Pump. It is suggested to check the battery once a month. · Disconnect the equipment from the animal, and stop all infusion · Supply AC power to the equipment to charge the battery for 5 hours at least · Supply power for the Covetrus ProMAX Syringe Pump only with the battery, start infusion at
5 ml/hour, and test the time until the battery runs down and the equipment is turned OFF – If the infusion time exceeds 10 hours, the battery is good – If the infusion time exceeds 7 hours but less than 10 hours, the battery starts deteriorating,
but it can be used temporarily – If the infusion time is less than 7 hours, and the battery reaches the service life, please replace
the battery
Replacing the Battery
Contact Covetrus®
After-Sale Service
This product has a free warranty period of 1 year from the purchase date. The warranty period starts at the invoiced date provided by Covetrus®.
Note: the machine damage caused by the following conditions is not covered by the free warranty: · Faults caused by unauthorized modification or maintenance due to improper use · Fire, flood, wind, earthquake, abnormal voltage, and other natural faults and damages · The machine is bumped or damaged due to improper operation during handling after purchase In case of damage or failure under the above circumstances, Triumph Medical can provide maintenance, but a certain fee will be charged accordingly.
27

Appendix Appendix Alarms and Solution

NO. Alarm Type

1

VTBI Near End

2

Syringe Near Empty

3

VTBI Infused

4

Syringe

Empty

5

Pressure Near

Threshold

6

Pressure

Drop

7

Pressure High

8

Battery Nearly

Empty

9

Battery Empty

10

No Battery

Inserted

Alarm Level
Low Low High High Middle High
Low
Low
High Low

Reason
During infusion, the remaining time of preset value reaches or is less than the set nearing completion time
The syringe is near empty status which is calculated by checking the liquid medicine remaining in the syringe by the current flow rate
The preset value infusion Completion
The liquid medicine in the syringe is empty
Pipeline pressure increases close to the preset blocking level
When the pipeline pressure is high, the pressure suddenly decreases
Line occlusion during infusion
Fluid/drug in the actual infusion line has high viscosity, but the system occlusion level is set too low
The Pressure Sensor is damaged
When power is supplied only with the built-in battery, under low battery, the alarm duration is >30min
Battery aging or the equipment charging circuit is faulty
When power is supplied by the built-in battery only, under low battery, the alarm duration is >30 minutes
Battery aging or the equipment charging circuit is faulty
Battery is removed

Solution
This alarm can’t be eliminated and waits till infusion completes
This alarm can’t be eliminated and waits till infusion completes
Press Stopbutton to stop alarm
Press Stopbutton to stop alarm
Check the connection of the pipeline, and press OKbutton to continue infusion
Check the connection of the infusion pipeline, and press OKbutton to continue infusion
Click Mute to silence, manually remove the reason for occlusion, and press Start button to continue infusion Raise the alarm Level, and press Startbutton to continue infusion Please contact Triumph Medical
The alarm automatically eliminates after connecting the external power supply
Please contact Triumph Medical
Immediately connect with the external power supply
Please contact Triumph Medical
Keep connected with the external power supply, reinstall the battery

28

NO. Alarm Type

11

No Power Supply

Alarm Level
Low

Reason
Under ON state, AC Power Supply is adopted, but the AC Power Cord is dropped during the process

Solution
The alarm automatically eliminates after connecting the external power supply

12

Check Syringe

13

Pump Idle

Alert

14

Standby Time Expired

15

KVO Finished

16

System Error

High Low Middle High High

Syringe drop off during infusion
After installing the syringe, under non- working or alarm state, it is not operated within the set time of the system
During standby, after reaching the standby time
KVO working time reaches 30 minutes, Covetrus® ProMAX Syringe Pump stops working
Internal failure or software exception

Reinstall the syringe
Click any button to stop
PressStopbutton to stop alarm
PressStopbutton to stop alarm
Turn OFF and restart If the alarm still exists, please contact Triumph Medical

Note: When the alarm rings, click the Muteicon on the screen to temporarily stop the sound alarm for 2 minutes.

Questions? 855-724-3461
Distributed by: Covetrus® North America 400 Metro Place North Dublin, OH 43017 covetrus.com

Manufacturer: Triumph Medical Services, Inc. 891 Bolger Court Fenton, MO 63026 888-962-0662

Reorder #080540
AH-ProMAXSyringePump-01 REV: 0423

References

• covetrus.com

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