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NOTE:
(2): The detector should be stored at 10 to 40 °C (50 to 104 °F) and less than or equal
to 90% RH in the plastic wrapped shipping box. (This should include two bags of
desiccant as well). The lowest temperature (e.g. 10 ºC (50 °F)) and humidity is
preferable. If they are to be stored outside of their shipping box or in the inner shipping
box without plastic wrapping they should be stored at 20 °C (68 °F) or less and 30% RH
or less. In terms of transportation, do not expose to temperatures below –20 ºC (–4 °F)
in its shipping box for more than 15 hours. The detector will reach the ambient
temperature after 20 to 25 hours. The detector should not be allowed to reach
temperatures less than –10 ºC (14 °F) or irreparable damage to the detectors scintillator
will occur. Care must be taken when removing a detector from a shipping box. If the
detector has been subject to cold temperatures for an extended period the detector in
the box should be allowed to sit in the plastic wrapped box to reach room temperature.
This will prevent condensation from occurring. Condensation on the detector can cause
irreparable damage to the electronics. Storage 10 to 40 ºC (50 to 104 °F); 10 to 90 %
RH, 250 day storage transportation –20 to +60 ºC (–4 to 140 °F) and 10 to 80% RH. The
Detector chiller HEAT DRY 1 is shipped within GE Healthcare packaging.
NOTE:
(3a): In use temperature limits specify the range where the system shall work. Operating
outside these limits could occur severe performance and reliability issues.
(3b): Recommended temperature limits specify the range where it is recommended to
adjust air conditioning control in order to warranty current operations inside the in use
range.
2.1.1 Relative Humidity and Temperature
Refer to
. To obtain relative humidity and temperature requirements for components not
specified in
, refer to the appropriate component Pre–Installation Manual listed in
2.1.2 Altitude and Atmospheric Pressure
Refer to
. To obtain altitude and atmospheric pressure requirements for components not
specified in
, refer to the appropriate component Pre–Installation Manual listed in
Table 3-2:
INSTALLATION ROOM
OF PRODUCT OR COM‐
PONENT
ALTITUDE (meters)
ATMOSPHERIC PRESSURE (kPa)
IN-USE
STORAGE / TRANS‐
PORT
IN-USE
STORAGE / TRANSPORT
MIN
MAX
MIN
MAX
MIN
MAX
MIN
MAX
Examination room
-30
2440
-30
2440
70
106
70
106
Technical room (see No‐
tice below)
-30
2440
-30
2440
70
106
50
106
Control room
0
2440
0
2440
N/A
N/A
N/A
N/A
Innova 2121-IQ/3131-IQ Biplane Cardiovascular Imaging System Pre-Installation Manual
GE Healthcare
Direction 5177951-4-1EN, Revision 1
Chapter 3 Physical Requirements of room
55
Summary of Contents for Innova 2121-IQ Biplane
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