E. Attaching the sensor to the patient cable
1. Refer to Fig. 8a. Properly orient the sensor connector and insert the sensor connector completely into the patient
cable connector.
2. Refer to Fig. 8b. Close the protective latch cover completely.
F. Disconnecting the sensor from the patient cable
1. Refer to Fig. 9a. Lift up the protective cover.
2. Refer to Fig. 9b. Pull firmly on the sensor connector to remove it from the patient cable.
NOTE: To avoid damage, pull on the sensor connector, not the cable.
CLEANING
To surface clean the sensor:
1. Remove the sensor from the patient and disconnect it from the attachment wrap and patient cable.
2. Remove the adhesive squares.
3. Clean the YI sensor by wiping it with a 70% isopropyl alcohol pad.
4. Allow the sensor to dry prior to placement on a patient.
or
1. If low-level disinfection is required, wipe all surfaces of the YI sensor and cable with a cloth or gauze pad saturated
with a 1:10 bleach/water solution.
2. Saturate another cloth or gauze pad with sterile or distilled water and wipe all surfaces of the YI sensor and cable.
3. Dry the sensor and cable by wiping all surfaces with a clean cloth or dry gauze pad.
To clean or disinfect the sensor using a soaking method:
1. Place the sensor in the cleaning solution (1:10 bleach/water solution), so that the sensor and desired length of cable
are completely immersed.
WARNING: Do not immerse the connector end of the sensor cable as this may damage the sensor.
2. Dislodge air bubbles by gently shaking the sensor and cable.
3. Soak the sensor and the cable for at least 10 minutes and not greater than 24 hours. Do not immerse the connector.
4. Remove from cleaning solution.
5. Place the sensor and the cable in room temperature sterile or distilled water for 10 minutes. Do not immerse the
connector.
6. Remove from the water.
7. Dry the sensor and cable with a clean cloth or dry gauze pad.
CAUTION:
• Do not use undiluted bleach (5–5.25% sodium hypochlorite) or any cleaning solution other than those recommended
herein because permanent damage to the sensor could occur.
• Do not immerse the connector on the YI cable in any liquid solution.
• Do not sterilize by irradiation, steam, autoclave, Gluteraldehyde (Cidex) or ethylene oxide.
• Using excessive force when removing the attachment wrap may damage the sensor.
SPECIFICATIONS
When used with Masimo SET® pulse oximetry monitors, or with licensed Masimo SET pulse oximetry modules and patient
cables, the RD YI sensors have the following specifications:
RD SET YI Sensor:
Body Weight
SpO
Accuracy, No Motion
2
SpO
Accuracy, Motion
2
SpO
Accuracy, Low Perfusion
2
Pulse Rate Accuracy, No Motion
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.
rms
Approximately two-thirds of the device measurements fell within ± A
The Masimo SET technology has been validated for no motion accuracy in human blood studies on healthy adult male and
1
female volunteers with light to dark pigmented skin in induced hypoxia studies in the range of 70–100% SpO
CO-Oximeter.
The Masimo SET technology has been validated for motion accuracy in human blood studies on healthy adult male and female
2
volunteers with light to dark pigmented skin in induced hypoxia studies while performing rubbing and tapping motions, at 2 to 4 Hz
Adults / Pediatrics / Infants
1
2
3
4
4
4
> 3 kg
2%
3%
2%
3 bpm
5 bpm
3 bpm
of the reference measurements in a controlled study.
rms
8
Neonate
1–3 kg
3%
3%
3%
3 bpm
5 bpm
3 bpm
against a laboratory
2
9024C-eIFU-0518