Cardinal Health Alaris 8000 Series, Directions For Use Manual

Page: 229 / 378

General Information
3-51 Alaris
®
System Directions for Use
Patient Controlled Analgesia Module Section
Configurable Settings (Continued)
NOTES:
€
This configuration setting is a shared setting between the
PCA Module and the Alaris
®
Syringe Module.

These values are configured in the
S
p
O
2
Module settings
within the Guardrails
®
Editor and can be changed by the
clinician by accessing Channel Options on the PCA Module.
‚
These values are configured in the
E
t
CO
2
Module settings
within the Guardrails
®
Editor and can be changed by the
clinician by accessing Channel Options on the PCA Module.
Specifications
Bolus Dose Range Configured according to hospital best-practice guidelines.
Bolus Volume after
Occlusion, Maximum
:
Bolus Volume at Intermediate Rate (
5
mL/h)
Occlusion Pressure Limit Bolus Volume
High
0.997
mL
Low
0.396
mL
Specifications and Symbols
Critical Volume : Maximum over-infusion which can occur in event of a single-fault condition will
not exceed
2%
of nominal syringe fill volume during loading and
1%
of maximum
syringe travel after syringe loading.
Delivery Units mcg, mcg/h, mg, mg/h, mL, mL/h
Dimensions :
4.5
"
W
x
15.0
"
H
x
7.5
"
D
(exclusive of security door)
Environmental Conditions : Operating Storage/Transport
Temperature Range: 41
-
104°F
-
4
-
140°F
(
5
-
40°C
) (-
20
-
60°C
)
Relative Humidity: 20
-
90% 5
-
85%
(Avoid prolonged exposure
Noncondensing Noncondensing
to relative humidity >85%)
Atmospheric Pressure: 525
-
4560
mmHg
375
-
760
mmHg
(
700
-
6080
hPa) (
500
-
1013
hPa)
Equipment Orientation : To ensure proper operation, PC Unit must remain in an upright position.