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47
References and Troubleshooting
Continuous Delivery Rechargeable Battery Pack
Life with screen intensity set to 3
Rate
Life
Volume
0.4 mL/hr
119 hrs
47.6 mL
1 mL/hr
89 hrs
89 mL
5 mL/hr
88 hrs
440 mL
10 mL/hr
86 hrs
860 mL
30 mL/hr
43 hrs
1290 mL
Classification
CF
J
, Class II
K
.
Moisture Protection
Splashproof (
E
) per IEC 60529.
Maximum Infusion Pressure
27.0 psi [1.86 bar].
Maximum Time to Occlusion Alarm
0.1 mL/hr - medication cassette reservoir:
108 minutes. CADD® administration set:
122 minutes.
10 mL/hr - medication cassette reservoir:
44 seconds. CADD® administration set:
122 seconds.
NOTE
: Values are nominal and based on
actual test data.
Bolus Volume at Occlusion Alarm
0.1 mL/hr - medication cassette reservoir:
0.107 mL. CADD® administration Set: 0.136 mL.
10 mL/hr - medication cassette reservoir:
0.116 mL. CADD® administration set: 0.124 mL.
NOTE
: Values are nominal and based on
actual test data.
Power Sources
Four AA (IEC LR6) alkaline batteries; AC
adapter; rechargeable battery pack.
Charging System for Internal Memory Backup
Battery
The internal memory backup battery utilizes
lithium manganese dioxide technology. It
charges whenever the pump is powered on and
has a 10 month memory capacity once it has
been charged for 250 hours at 20°C (68°F).
System Operating Temperature
2°C to 40°C (36°F to 104°F).
System Storage and Transportation Temperature
–20°C to 60°C (–4°F to 140°F).
Relative Humidity
20% to 90% relative humidity, non-condensing.
Atmospheric Pressure
70 kPa (10.2 psi) to 106 kPa (15.4 psi).
System Delivery Accuracy
± 6% (nominal). At low infusion rates, this
accuracy may not be achieved for short periods.
During the total infusion time, the accuracy
averages out.
WARNING:
•
Ensure that the ± 6% system delivery accuracy
specification is taken into account when
programming the pump and/or filling the
reservoir. Failure to do so may result in
medication in the reservoir becoming depleted
sooner than expected. If the pump is being used
to deliver critical or life sustaining medication,
the interruption in the delivery of medication
could result in patient injury or death.
•
System delivery inaccuracies may occur as
a result of back pressure or fluid resistance,
which depends upon drug viscosity, catheter
size, and extension set tubing (for example,
microbore tubing), and placing the infusion
reservoir and/or pump above or below the level
of the patient. System delivery inaccuracy may
result in under or over-delivery of medication,
which could result in death or serious injury to
the patient.
System Definition
CADD
®
-Solis pump with:
•
An attached medication cassette reservoir
and CADD
®
extension set or
•
an attached CADD
®
administration set or
CADD
®
-Solis pump with:
•
an attached medication cassette reservoir
with flow stop feature and CADD
®
extension
set or
•
A CADD
®
administration set with flow stop
feature.
Summary of Contents for CADD-Solis
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