69
value may be set between 0.5 – 3.8
ml/hr in increments of 0.1 ml/hr during
configuration. In addition, the pump
also has a configurable single bubble
alarm that can be set between 0.02 –
0.3 ml in increments of 0.01 ml.
The pump display indicates if the alarm
is a Single bubble alarm or an
Accumulated Air alarm and stops the
infusion thus requiring intervention
from the user to address the alarm.
“Upstream sensor” 9 levels from -90 mmHg to -160 mmHg
(pressure reduction)
Occlusion alarm pressures
(downstream pressure) 9 levels from 225mmHg to 900 mmHg
Alarm volume 9 levels from 1 (59dBA) to 9 (74dBA)
Mechanical occlusion pressure limit
Occlusion alarm pressure max. 1575 mmHg
under fault conditions (210 kPa).
Maximum posts occlusion bolus volume
2ml.
Pump log Logs are accessed via the service
program.
Pump logs include history log of 1000
past entires, alarm log, key stroke and
notes log. Refer to HiBaSed IFU for
more information.
Caution: If a wrench is displayed and/or the yellow, red and blue
LEDs blink, then the pump is in the service mode and cannot be used on a
patient. The pump must then be checked by a service technician.
Note:
Th
e technical data stated in this Instructions for Use manual were
determined with the Infusomat® Space line (870 0036 SP). These technical data
can change when using different set configurations.
• Use only pressure proof and compatible disposable items (min. 2 bar/
1500 mm Hg) to avoid influencing performance data - which would result in
impairing patient safety.
Level 1
Level 5
Level 9
[mmHg]
Time to occlusion alarm [min] at rate Max bolusOcclusion pressure
[1 mL/h]
typ. 226 09:07
typ. 563
typ. 900
25:53
46:50
[25 mL/h]
00:33
01:14
02:06
[100 mL/h]
00:07
00:15
00:24
[mL]
0.0347
0.0987
0.1787
Chapter 8
TECHNICAL DATA