Masimo RED DCI Manual De Instrucciones página 4

• Note: The sensor is provided with X-Cal® technology to minimize the risk of inaccurate readings and unanticipated loss
of patient monitoring. Replace the sensor when the patient monitoring time is exhausted.
INSTRUCTIONS
A. Site selection
• Choose a site that is well perfused and least restricts a conscious patient's movements. The ring or middle finger of the
non-dominate hand is preferred.
• Alternatively, the other digits on the non-dominate hand may be used. Always choose a site that will completely cover
the sensor's detector window. The great toe or long toe (next to the great toe) may be used on restrained patients or
patients whose hands are unavailable.
• Site should be cleaned of debris and dry prior to sensor placement.
B. Attaching the sensor to the patient
1. Refer to Fig. 1. Open the sensor by pressing on hinge tabs. Place the selected digit over the sensor window of the
sensor. The fleshiest part of the digit should be covering the detector window in the lower half of the sensor. The top
half of the sensor is identified by the cable. The tip of the finger should touch the raised digit stop inside the sensor.
If the fingernail is long, it may extend over and pass the finger stop.
2. Refer to Fig. 2. The hinged tabs of the sensor should open to evenly distribute the grip of the sensor along the length of
the finger. Check position of sensor to verify correct positioning. Complete coverage of the detector window is needed
to ensure accurate data.
3. Refer to Fig. 3. Orient the sensor so that the cable will be running towards the top of the patient's hand. Connect the
sensor connector to a patient cable or directly to the device.
C. Disconnecting the Sensor from the Patient Cable
1. Place thumb and index finger on gray buttons on either side of the patient cable connector.
2. Refer to Fig. 4. Press firmly on the gray buttons and pull to remove the sensor.
CLEANING
To clean the sensor, first remove it from the patient and disconnect it from the patient cable. You may then clean the sensor
by wiping it with a 70% isopropyl alcohol pad. Allow the sensor to dry prior to placement on a patient.
CAUTION: To prevent damage, do not soak or immerse the sensor in any liquid solution. Do not sterilize by irradiation, steam,
autoclave or ethylene oxide.
SPECIFICATIONS
When used with Masimo rainbow SET pulse oximetry monitors or with licensed Masimo rainbow SET pulse oximetry modules
Red DCI and DCI-P reusable sensors have the following specifications:
Sensor
Body Weight
Application site
SpO Accuracy, No Motion (70 - 100%)
2
2
SpO Accuracy, Motion
2
3
SpO Accuracy, Low Perfusion
2
Pulse Rate Accuracy, No Motion (25 - 240 bpm)
4
Pulse Rate Accuracy, Motion
Pulse Rate Accuracy, Low Perfusion
NOTE:
A accuracy is a statistical calculation of the difference between device measurements and reference measurements. Approximately two-thirds of the device
rms
measurements fell within ± A of the reference measurements in a controlled study.
rms
1
The Masimo SET Technology has been validated for no motion accuracy in human blood studies on healthy adult male and female volunteers with light to dark pigmented skin in induced
hypoxia studies in the range of 70-100% SpO
2
The Masimo SET Technology has been validated for motion accuracy in human blood studies on healthy adult male and female volunteers with light to dark pigmented skin in induced
hypoxia studies while performing rubbing and tapping motions, at 2 to 4 Hz at an amplitude of 1 to 2 cm and a non-repetitive motion between 1 to 5 Hz at an amplitude of 2 to 3 cm in induced
hypoxia studies in the range of 70-100% SpO
3
The Masimo SET Technology has been validated for low perfusion accuracy in bench top testing against a Biotek Index 2 simulator and Masimo's simulator with signal strengths
of greater than 0.02% and transmission of greater than 5% for saturations ranging from 70% to 100%. This variation equals plus or minus one standard deviation which
encompasses 68% of the population.
4
The Masimo SET Technology has been validated for pulse rate accuracy for the range of 30-240 bpm in bench top testing against a Biotek Index 2 simulator and Masimo's simulator
with signal strengths of greater than 0.02% and transmission of greater than 5% for saturations ranging from 70% to 100%. This variation equals plus or minus one standard deviation
which encompasses 68% of the population.
Red DCI
> 30 kg
Finger
1
4
3 bpm
5 bpm
3 bpm
4
against a laboratory co-oximeter. This variation equals plus or minus one standard deviation which encompasses 68% of the population.
2
against a laboratory co-oximeter. This variation equals plus or minus one standard deviation which encompasses 68% of the population.
2
2%
3%
2%
4
Red DCI-P
10 - 50 kg
Finger
2%
3%
2%
3 bpm
5 bpm
3 bpm
4116J-eIFU-0721