6
6688F-eIFU-0818
4. Refer to
Fig. 3c.
Wrap the foam wrap around the foot and ensure that the emitter window (red star) aligns directly
opposite of the detector. Be careful to maintain proper alignment of the detector and emitter windows while attaching
the foam wrap to secure the sensor.
5. Refer to
Fig. 3d.
Check the sensor to verify correct positioning and reposition if necessary.
C) Attaching the Sensor to the Patient Cable
M-LNCS
Refer to
Fig. 4.
Insert the sensor connector completely into the patient cable connector and lock into place.
LNCS
Refer to
Fig. 5.
Insert the sensor connector completely into the patient cable connector (1). Completely close the protective
cover (2).
D) Reattachment
• The sensor may be reapplied to the same patient if the emitter and detector windows are clear and the adhesive still adheres
to the skin.
• If the adhesive no longer adheres to the skin, use a new sensor.
NOTE:
When changing application sites, or reattaching the sensor, first disconnect sensor from the patient cable.
E) Disconnecting the Sensor from the Patient Cable
M-LNCS
Refer to
Fig. 7.
Pull firmly on the sensor connector to remove it from the patient cable.
LNCS
Refer to
Fig. 8.
Lift the protective cover to gain access to the sensor connector (1). Pull firmly on the sensor connector to
remove from the patient cable (2).
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 Set and Masimo compatible Pulse Oximeters:
M-LNCS/LNCS Specialty Sensor
Trauma (Adult)
Newborn (Infant/Pediatric)
Newborn (Neonatal)
5
NON
STERILE
LATEX
Title: Graphics, Sensor/Cable symbols, 03/06
GR-14231
DRO-13914
-40 C
+70 C
+1060 hPa - +500 hPa
795 mmHg - 375 mmHg
5%-95% RH
5%
95%
%
Body Weight
> 30 kg
3–10 kg
10–30 kg
< 3 kg
Application Site
Finger or toe
Thumb or great toe
Finger or toe
Hand or foot
SpO
2
Accuracy, No Motion
1
2%
2%
5
2%
3%
SpO
2
Accuracy, Motion
2
3%
3%
3%
3%
SpO
2
Accuracy, Low Perfusion
3
2%
2%
2%
3%
Pulse Rate
Accuracy, No Motion
4
3 bpm
3 bpm
3 bpm
3 bpm
Pulse Rate Accuracy, Motion
4
5 bpm
5 bpm
5 bpm
5 bpm
Pulse Rate Accuracy, Low Perfusion
4
3 bpm
3 bpm
3 bpm
3 bpm
When used with Nellcor and Nellcor Compatible Pulse Oximeters:
6
SpO
2
Accuracy, No Motion
2%
2%
2%
3%
Pulse Rate Accuracy, No Motion
3 bpm
3 bpm
3 bpm
3 bpm
NOTE:
A
rms
accuracy is a statistical calculation of the difference between device measurements and reference measurements.
Approximately two-thirds of the device measurements fell within ±
A
rms
of the reference measurements in a controlled study.
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
against a laboratory co-
oximeter.
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
2
against a laboratory co-oximeter.
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%.
4
The Masimo SET Technology has been validated for pulse rate accuracy for the range of 25–240 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%.
5
The saturation accuracy of the Neonate and Preterm sensors were validated on adult volunteers and 1% was added to account for
the properties of fetal hemoglobin.
6
Not validated for Motion and Low Perfusion accuracy using Nellcor Technology.
