
OPERATION MANUAL
HEMOTHERM MODEL 400CE
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Reusable Blanket
Cincinnati Sub-Zero reusable blankets are constructed from biocompatible
polyurethane/urethane. Some stains and debris may be wiped away with mild soap and
water. For cleaning and disinfecting, always use conventional hospital-approved topical
cleaners and disinfectants that do not contain alcohol. Avoid alcohol and other strong,
undiluted disinfectants. These may cause staining of the device’s outer skin. Thoroughly
rinse product with clear water to remove any residue from cleaning solutions. DO NOT use
gas sterilization or autoclaving for cleaning and disinfecting the blankets.
To drain the water from the reusable blankets shut off the power to the unit. The water in
the PlastiPad will automatically drain back into the unit. Allow it to fully drain before
disconnecting the blanket from the unit or removing from bed, stretcher, or table.
To store Plastipad blankets, loosely coil the hose lengthwise into the center of the blanket.
Fold the blanket lengthwise into the center, 1/3 from the left side and 1/3 from the right
side. Do not fold the blankets width-wise, as doing so will crimp the tubing.
For cleaning and disinfecting of the Gelli-Roll, always use conventional hospital-approved
topical equipment cleaners and disinfectants that do not contain alcohol. The Gelli-Roll is
washable at temperatures of approximately 108°F (42.2°C). Make sure the Gelli-Roll
does not enter washing machines or dryers. Avoid alcohol and other strong, undiluted
disinfectants. These may cause st
aining or hardening of the pad’s outer skin. Thoroughly
rinse product with clear water to remove any residue from cleaning solutions. A solution
of 1:10 parts bleach to water can also be used for cleaning process.
Disposal of blankets are done in a means consistent with hospital/institution policy/protocol
for patient contact items.
Disposable, Single-Patient Use Blankets
The reusable blanket maintenance procedures do not apply to the disposable, single-
patient use blankets. Disposal of blankets are done in a means consistent with
hospital/institution policy/protocol for patient contact items.
3.9
REMOVE FROM SERVICE ALARM (RFS)
The Remove from Service (RFS) alarms are a visual and audio indication of a possible
error condition in the temperature control system. The RFS alarms will require the unit to
be inspected by the hospital's biomedical or maintenance department and, if required,
repaired immediately. The following are an indication that an RFS alarm condition has
occurred:
An “EE” on the HEAT side temperature display and an error number (2, 3, 5, or 6)
on the COOL side temperature display.
Temperature in the HEAT side reservoir exceeding the secondary high limit safety
is also an RFS alarm and will be indicated by the HIGH TEMP. LIMIT red LED
indicator and the beeper.
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