• The Pump and Syringe Modules are designed to
stop fluid
flow under alarm conditions
. Periodic patient monitoring
must be performed to ensure the infusion is proceeding as
expected. It is a
positive displacement delivery system
,
capable of developing positive fluid pressures to overcome
widely varying resistances to flow encountered in practice,
including resistances to flow imposed by small gauge
catheters, filters and intra-arterial infusion. It is neither
designed nor intended to detect infiltrations and will not
alarm under infiltration conditions.
• The use of positive displacement infusion devices ported
together with
gravity flow infusion
systems into a
common
IV
site may impede the flow of common "gravity
only" systems, affecting their performance. Hospital/facility
personnel must ensure the performance of the common
IV
site is satisfactory under these circumstances.
• To prevent a
potential free-flow condition
, ensure no
extraneous object (for example, bedding, tubing, glove)
is enclosed or caught in the Pump Module door.
•
Each time the Alaris
®
System is turned on
, verify
and/or set the monitoring mode, resistance alert, and/or
pressure alarm limit. If the monitoring mode,
resistance alert, and/or pressure alarm limit are not
verified, the instrument may not operate within the
desired occlusion detection parameter(s).
WARNINGS
General Information
General Information
2-73
Warnings and Cautions
General
Alaris
®
System Directions for Use
Pump and Syringe Modules Section
ALARM
INFUSE
STANDBY
CHANNEL
SELECT
CHANNEL
OFF
PAUSE
RESTART
RATE (mL/h)
CHANNEL
SELECT
CHANNEL
OFF
RESTART
PAUSE
ALARM
INFUSE
STANDBY
CHANNEL
SELECT
CHANNEL
OFF
RESTART
PAUSE
ALARM
INFUSE
STANDBY
ALARM
INFUSE
STANDBY
CHANNEL
SELECT
CHANNEL
OFF
PAUSE
RESTART
RATE (mL/h)
Содержание Alaris 8000 Series
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