Masimo RD rainbow SET Serie Mode D'emploi page 3

RD rainbow SET® Series
Patient Cables
Reusable
INDICATIONS
The RD rainbow SET® Series patient cables have the same indications for use as the applicable sensors. Please see the
compatible sensor's directions for use for indications for use and prescribed information.
DESCRIPTION
The RD rainbow SET Series patient cables are used with RD SET® Series sensors.
RD rainbow SET Series patient cables are for use only with devices containing Masimo® SET® or Masimo rainbow SET®
technology Version 7.1 or higher or licensed to use rainbow® compatible sensors. Consult individual oximetry system
manufacturers for compatibility of particular devices and sensor models. Each device manufacturer is responsible for
determining whether their devices are compatible with each sensor model.
RD rainbow SET Series patient cables have been verified using Masimo rainbow SET technology.
WARNING: Masimo sensors and cables are designed for use with devices containing Masimo SET oximetry or licensed
to use Masimo sensors.
WARNINGS, CAUTIONS, AND NOTES
• Always refer to the oximeter module operator's manual for complete instructions or additional instructions.
• Ensure the cable is physically intact, with no broken or frayed wires or damaged parts. Visually inspect the cable
and discard if cracks or discoloration are found.
• All sensors and cables are designed for use with specific monitors. Verify the compatibility of the monitor, cable
and sensor before use, otherwise degraded performance and/or patient injury can result.
• Carefully route patient cable to reduce the possibility of patient entanglement or strangulation.
• Failure to properly connect the sensor or the oximeter module to the cable may result in intermittent readings,
inaccurate results, or no reading.
• To avoid damage to the cable, always hold it by the connector rather than the cable when connecting or
disconnecting either end.
• To prevent damage, do not soak or immerse the sensor or cable in any liquid solution. Do not attempt to sterilize
the cable or sensor.
• Do not attempt to reprocess, recondition or recycle Masimo sensors or patient cables as these processes may
damage the electrical components, potentially leading to patient harm.
• Caution: Replace the cable when a replace cable message is displayed, or when a low SIQ message is consistently
displayed while monitoring consecutive patients after completing the low SIQ troubleshooting steps identified in
the monitoring device operator's manual.
• Note: The cable is provided with X-Cal® technology to minimize the risk of inaccurate readings and unanticipated
loss of patient monitoring. The cable will provide up to 17,520 hours of patient monitoring time. Replace the cable
when the patient monitoring time is exhausted. Some legacy monitoring devices do not distinguish between the
cable and the sensor. In these devices, a replace sensor or similar message could pertain either to the sensor or
the cable.
INSTRUCTIONS
A) Connect the RD rainbow SET Series patient cable to the Device
1. Connect the device connector of the patient cable to the mating connector of the device.
2. Ensure the patient cable connector is fully engaged with the device. A tactile or audible click of connection should be heard.
B) Connect the RD rainbow SET Series patient cable connector to an RD SET disposable sensor connector
1. Refer to Fig. 1. Orient the sensor connector to the patient cable connector as shown.
2. Refer to Fig. 2. Insert the sensor connector completely into the patient cable connector until it locks in place
as shown.
C) Connect the RD rainbow SET Series patient cable connector to the RD SET reusable sensor connector
1. Refer to Fig 3. Orient the sensor connector to the patient cable connector, as shown.
2. Refer to Fig. 4. Insert the sensor connector completely into the patient cable connector. Close the sensor connector
cover over the patient cable connector until it locks in place.
D) Disconnect the RD rainbow SET Series patient cable connector from the RD SET disposable sensor connector
1. Refer to Fig 5. Pull firmly on the sensor connector to remove it from the patient cable.
DIRECTIONS FOR USE
Not made with natural rubber latex
LATEX
3
en
Non-Sterile
9000G-eIFU-0121