Datascope Accutorr Plus Service Manual page 50

1.3.10.3 Sequence for establishing SpO2 with Masimo Set® Pulse Oximetry*
* This feature applicable only if available or installed on your unit.
1. Select the appropriate sensor for the patient from the table below. All sensors below
are non-sterile and can be used during patient movement.
MASIMO® SENSOR FAMILY
SELECTION PART NUMBER | PATIENT SIZE DISPOSABLE/
REUSABLE
LNOP® - Adt Adult 0600-00-0043-01 > 30 kg. Disposable
Disposable Finger Sensor
LNOP® -Pdr Pediatric/ 0600-00-0044-01 10 to 50 kg. Disposable
Slender Digit Disposable
Sensor
LNOP® - Neo Neonatal 0600-00-0045-01 < 10 kg. Disposable
Disposable Sensor
LNOP® - Neo Pt Neonatal | 0600-00-0046-01 <1kg. Disposable
Pre-term Disposable Sensor
LNOP® - DCI Adult 0600-00-0047 > 30 kg. Re-usable
Reusable Finger Sensor
PC12 Patient Cable 0012-00-1099-02 Al Re-usable
Extension
2. Attach the PC12 Patient Cable (P/N 0012-00-1099-02) to the sensor and plug che
other end of the patient cable into the SpO2 connector (15)
NOTE: Do not place the sensor on an extremity with an invasive catheter or blood
pressure cuff in place.
NOTE: Ensure proper routing of patient cable to avoid entanglement and/or
strangulation.
CAUTION: When equipped with MASIMO® Sp02, use only MASIMO® oxygen transducers
including MASIMO LNOP® patient dedicated adhesive sensors and MASIMO
PC12* Patient Cable. Use of other oxygen transducers may cause improper oximeter
performance.
CAUTION: Tissue damage or inaccurate measurements may be caused by incorrect sensor
application or use, such as wrapping it too tightly, applying supplemental tape,
failing to inspect the sensor site periodically, or failing to position it
appropriately. Carefully read the sensor directions for use, the Accutorr Plus
operating instructions, and all precautionary information before use.
CAUTION: Excessive ambient light may cause inaccurate measurements. Cover the sensor site
with opaque material.
CAUTION: Inaccurate measurements may be caused by incorrect sensor application or use;
significant levels of dysfunctional hemoglobins, (¢.g., carboxyhemoglobin or
methemoglobin); or intra-vascular dyes such as indocyanine green methylene blue;
exposure to excessive illumination, such as surgical lamps (especially ones with a
xenon light source), bilirubin lamps, fluorescent lights, infrared heating lamps, or
direct sunlight; excessive patient movement; venous pulsations; electro-surgical
interference; and placement of a sensor on an extremity that has a blood pressure cuff,
arterial catheter, or intra-vascular line.
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Revised 12/20/00
Accutorr Plus Service Manual
Chapter 1, Operation