Promax 7350370080540 Syringe Pump 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.

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.

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.

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.

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.

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.

The operator shall guarantee that the inputted infusion parameters of this equipment are the same as the

medical advice before starting the infusion.

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.

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

ground earth.

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.

This equipment must be operated by trained

professional medical care personnel.

This equipment does not apply to blood

transfusion.

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

accident.

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 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.

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 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 lm.

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.

This equipment can't be used in locations with radiological installation, magnetic resonance equipment, or places with

high-pressure oxygen therapy.

Please keep the equipment away from the AC Power socket for a certain distance to avoid uid/drug splashing or

dropping in the socket. Otherwise, it may possibly cause a short circuit.

Symbols

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

Lot Number

Attention, consult

accompanying documents

Non-Ionizing Radiation

Environment-friendly use period

(20 years)

Date of Manufacture

Deﬁbrillation Proof

Type CF Applied Part

Serial Number

Unlock

Class I Equipment

Alternating Current

Input and output

Handle with care

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

Marks Description Marks Description

IP34

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

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

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

Electric Protection Type Class I

Electric Protection Level Deﬁbrillation proof type CF applied part

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 syringe pump

Safety Classiﬁcation

Compatible Syringes 3 ml, 5 ml, 10 ml, 20 ml, 30 ml, 50/60 ml

System Accuracy ≥1ml/h, ±2% 1ml/h, ±5%

Infusion 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

Speciﬁcation Parameters

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 242.5 (w) x 111 (d) x 126.5 (h) mm

Weight 1.7 kg, 3.75 lbs

Speciﬁcation Parameters (continued)

AC Power Supply 100-240V 50/60Hz

Input Power 50VA

DC Power Supply DC 12V

Battery Speciﬁcations 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)

Power Supply

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: 15-95%, 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: 50-106 kPa

Environment

Alarm Signal Sound Pressure Level 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)

Alarm Information 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

Alarm

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

Safety Standard

Appearance

Front View

Part Number Name

Handle Control the Covetrus® ProMAX Syringe Pump

push-pull sliding box and clip

Slider Box

Pressure Sensor Detect the pressure of the syringe

Syringe Clip Clamp the syringe plunger

Leadscrew

Syringe Fixture Lever Pull forward, turn 90° right or left,

and install the syringe into the slot.

Keep the extension line straight and neat

Operation Panel

Part Number Name

Touch Screen

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.

AC Indicate Light When connected to the AC power supply,

the AC indicator light is on.

Alarm Indicator Light While pump alarms, the indicator light glitter, different

level, different frequencies and color, for more

information, please refer to page 21

Running Lights

Start/Stop

Bolus/Purge

Home Enter system home page

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.

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.

Syringe Apparatus Syringe apparatus indication icon

Indication Icon

Lock Screen Unlock state icon is

Indication Icon

WIFI Indicates WIFI connection state

Indication Icon

Battery Charging Display the current battery charging state

Indication Icon

Battery Status Battery life percentage is displayed on the left side of the icon

Indication Icon Battery icon may show the following states:

Icon Paraphrase Description

Typical Interface Icon Paraphrase

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.

Start Click this icon to start infusion

Stop Click this icon to stop infusion

Bolus/ 1. During infusion, it is aBolusfunction–click it to start fast infusion

Purge 2. Before infusion starts, it is aPurgefunction–click it to exhaust air

from the syringe

Home Click this icon, return to the main interface

Icon Paraphrase Description

Backspace Button Click it to backspace and delete

Shift Button Click it to switch the capital and lowercase English letters

Cancel Button Click it to cancel editing and exit

OK Button Click it to save editing and exit

Icon Paraphrase Description

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

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 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

Please put the packing materials out of reach of children. Please obey local laws and regulations when

disposing of items.

•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

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

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.

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

• ClickSetting Commonly used Syringe brandt o choose syringe brand if not selected

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®.

•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 size–selecting 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

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.

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 the Bolus on the Touch Screen, set two

parameters among bolus infusion volume, rate, and time, and click Start ; it will beep at every 1 ml

infused. After the bolus infusion is ﬁnished, the equipment will return to the previous infusion rate

•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

Promax 7350370080540 Syringe Pump User manual

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