Daiwha DI-6000, User Manual

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Safety Instructions
3

Replace the battery if its usage time significantly decreases even in full charge condition.

Contact the dealer to replace the battery.
Using for other purposes

Do not use product if it is wet.

Do not open or disassemble the product.

To prevent errors, check if the labels are attached on the infusion pump and tube.

Check the infusion pump setting and monitor the patient to check for extremely high or low
dose.

Be sure to plan and prepare for failures of the infusion pump in advance.

All possible actions must be taken to prevent and cope with pump issues.

Pressure is eliminated when the Occlusion alarm occurs because the Anti-Bolus function is
automatically activated in which unintended infusion does not occur. Be careful not to inject
medication before discharging pressure

The maximum infusion pressure is 1050 mmHg.

Injection is immediately stopped in failure status so unintended infusion does not occur.
When the failure continuously occurs, contact the dealer or headquarters.

Check for infusion difference in the following situation.

In case of using fluid of high viscosity such as Dextrose 50 %.

When infusion is not made because the active time of the occlusion alarm is long
due to low flow rate of the infusion.

When using in the environment other than ambient temperature of 10-40
℃
,
relative humidity of 20-90 %, and atmospheric pressure of 70-106 kha.
Cleaning the product

Do not sterilize device with autoclave or EO (Ethylene Oxide) gas.

Do not use thinner, solvent, benzene, ammonia, or acetone to clean the product. Use wet
gauze and wipe out moisture with smooth dry fabric.

Do not soak the product in water or dry it by force.
When injecting drug

Regularly check for product operation and patient status.

Use the Lock function for safe use for settings not to be changed even though pressing any
buttons during operation.

Inspect to prevent I.V Set damage such as leakage or filter burst.
Using I.V Set

Use I.V Set exclusive for drug infusion pump.

The intended flow rate may not be satisfied if the designated I.V Set is not used and
this may cause air or occlusion alarms. If the designated I.V Set cannot be used,
inquire the dealer or headquarters.