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Operating Environment
•
Ambient temperature: 10°C to +35°C
•
Relative humidity: 30% to 90%
•
Atmospheric pressure: 800hPa to 1060hPa
•
Shock (without packing): 10 G, duration 6 ms
Environment for Storage
•
Ambient temperature: -10°C to +55°C
•
Relative humidity range: 10% to 95%
•
Atmospheric pressure: 700 hPa to 1060 hPa
NOTE
It is recommended to remove the battery if the device is stored over two weeks.
Environment for Transportation
•
Ambient temperature: -40°C to +70°C
•
Relative humidity range: 10% to 95%
•
Atmospheric pressure: 500 hPa to 1060 hPa
•
Vibration, sinusoidal: 10 Hz to 500 Hz: 0.5G
•
Shock: 30 G, duration 6 ms
•
Bump: 10 G, duration 6 ms
NOTE
It is recommended to remove the battery if the device is stored over two weeks.
Regulations
•
U.S. Federal law restricts this device to be sold and distributed, and it should be used only
by or on the order of a physician.
•
This device has been tested and found to comply with the limits for medical devices to the
IEC 60601-1-2: 2014. These limits are designed to provide reasonable protection against
harmful interference in a standard medical installation. If this device does cause harmful
interference to other devices, which can be determined by turning the system oī and on,
the user is encouraged to try to correct the interference through one or more of the
following measures: Reorient or relocate the receiving device.
•
Increase the separation between the system and other devices.
•
Connect the device to an outlet on a circuit diīerent from that to which the
other device(s) are connected.
•
Consult the manufacturer or Įeld service technician for help.
•
The International Electrotechnical Commission sets the essential requirements for electri-
cal and electronic equipment that may disturb or be disturbed by other equipment. The
device complies with these requirements as shown in the tables in “Symbols and standards:
EMC” (ї 51). Follow the guidance in the tables for use of the device in an electromagnetic
environment.
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