•
T his device should not be used adjacent to or stacked with other equipment. If adjacent or stacked use is necessary, the device should be observed carefully to verify
normal operation.
•
The accuracy of the SpO
measurement may be affected if the total cable length (including extension cables) is greater than 3 meters.
2
•
T he use of accessories, sensors, and cables other than those specified by NONIN (except transducers and cables sold by NONIN as replacement parts for internal
components) may result in increased emission and/or decreased immunity of this device.
•
T his pulse oximetry system is designed to determine the percentage of arterial oxygen saturation of functional hemoglobin. Significant levels of dysfunctional hemoglobin,
such as methemoglobin, might affect the accuracy of the measurement.
•
T he XPOD oximeter has motion tolerant software that minimizes the likelihood of motion artifact being misinterpreted as good pulse quality. In some circumstances,
however, the XPOD oximeter may still interpret motion as good pulse quality. This covers all available outputs.
•
T his equipment complies with International Standard EN 60601-1-2:2001 for electromagnetic compatibility for medical electrical equipment and/or systems. This standard
is designed to provide reasonable protection against harmful interference in a typical medical installation. However, because of the proliferation of radio frequency
transmitting equipment and other sources of electrical noise in healthcare and other environments, it is possible that high levels of interference due to close proximity or
strength of a source might disrupt the device's performance. Medical electrical equipment needs special precautions regarding EMC, and all equipment must be installed
and put into service according to the EMC information specified in this document. Portable and mobile RF communications equipment can affect medical electrical
equipment.
For more information about required safety and regulatory requirements for medical devices, refer to EN865 and IEC 60601-1. Additional safety information can be found in the
labeling provided with each Nonin sensor.
iNtrOductiON
Your clinician may have supplied an oximeter for use with the DV5M SmartLink system. Connecting an oximeter to the SmartLink allows collection and storage of oximetry
data (oxygen saturation and pulse rate).
When using the optional oximeter with the SmartLink, follow the directions below for connecting the oximeter. The only oximeter compatible with this product is the Nonin
XPOD Oximeter. Use only the Nonin 8000AA, 8000Q, 8000SL or 8000SM sensors. Once the oximeter is plugged into the SmartLink, the oximeter will be powered and ready
for use.
Parts aNd accEssOriEs
The DV5M-697 Oximeter Kit contains the following items:
1. 9054D-693
Nonin XPOD Oximeter
2. 8000SM
Nonin Sensor
cONNEctiNG thE OximEtEr (figure 1)
1. P lug the oximeter into the bottom circular connector on the side of the DV5M SmartLink Module.
2.
Connect the supplied sensor to the oximeter. Match the two arrows on each end of the cables when inserting
the oximeter to the sensor.
3. W hen an oximeter is first connected and the sensor placed onto the finger, a visual notification will be
displayed after about ten (10) seconds to signal the presence of new oximetry (SpO
displayed on the CPAP LCD.
4. P ulse Rate (PR) and oximetry (SpO
A display screen on the LCD display shows real-time SpO
values will be displayed as "***" if the oximeter is not connected or if valid data is not available. This feature is to
confirm that the oximeter is connected and working properly. If the "***" persists, check connections and verify
proper sensor placement and consult the sensor instructions for troubleshooting.
If the sensor is removed from the finger or the signal is lost for more than 10 seconds, the unit will begin to display
a visual notification every 8 seconds until the oximeter is re-secured or sensor is replaced onto the finger or a
timeout threshold of one minute is reached.
If the oximeter is unplugged from the SmartLink, no notification will occur and the unit will cease logging oximetry data.
The DV5M SmartLink is capable of storing 72 hours of oximetry data (9 days at 8 hours per day).
attachiNG thE sENsOr
For instructions on attaching the sensor, refer to the respective pulse oximeter sensor package insert.
NOTE–The sensor will not function properly if there is nail polish on your fingernails.
NOTE–Check that the sensor is not damaged. If damaged, contact your equipment supplier.
NOTE–Do not attach the sensor to the oximeter until you are ready to start using the device.
startiNG trEatmENt
Start treatment as described in your IntelliPAP
A-M697
) data is available on the SmartLink menus.
2
and Pulse Rate (updated once every second). Both
2
or SleepCube
Instruction Guide. The SmartLink will automatically collect and store treatment data.
®
®
1
) data. SpO
will be
2
2
Connecting the Oximeter to the DV5M SmartLink Module.
EN - 3