E. Disconnecting the sensor from the patient cable
1. Refer to Fig. 8. Lift up the protective cover.
2. Refer to Fig. 9. 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
CAUTION:
• Do not use undiluted bleach (5–5.25% sodium hypochlorite) or any cleaning solution other than those recommended
here because permanent damage to the sensor could occur.
• To prevent damage, do not soak or immerse the connector in any liquid solution.
• Do not sterilize by irradiation, steam, autoclave, Gluteraldehyde (Cidex) or ethylene oxide.
To surface clean the sensor
1. Remove the sensor from the patient and disconnect it from the patient cable.
2. Remove the adhesive pad by pulling on white tab and discard. Any residue left by adhesive can easily be removed and
cleaned by wiping with 70% isopropyl alcohol.
3. Clean the RD SET TF-I sensor by wiping it with a 70% isopropyl alcohol pad or mild detergent.
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 RD SET TF-I 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 RD SET TF-I 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: To prevent damage, do not soak or immerse the connector in any liquid solution.
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.
SPECIFICATIONS
When used with Masimo SET pulse oximetry monitors, or with licensed Masimo SET pulse oximetry modules and patient
cables, the RD SET TF-I sensors have the following specifications:
Sensor:
Body Weight
Application Site
SpO
Accuracy, No Motion
1
2
Pulse Rate Accuracy, No Motion
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 female volunteers with light
1
to dark pigmented skin in induced hypoxia studies in the range of 70–100% SpO
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
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%.
COMPATIBILITY
This sensor is intended for use only with devices containing Masimo SET® oximetry or pulse oximetry monitors
licensed to use RD SET TF-I sensors. Each sensor is designed to operate correctly only on the pulse oximetry
systems from the original device manufacturer. Use of this sensor with other devices may result in no or improper
performance.
For Compatibility Information Reference: www.Masimo.com
2
RD SET TF-I
> 30 kg
Forehead
2%
3 bpm
of the reference measurements in a controlled study.
rms
against a laboratory CO-Oximeter.
2
5
9023D-eIFU-0618