Masimo RD SET YI Guia De Inicio Rapido página 5

RD SET™ YI
SpO2 Multisite Reusable Sensor and
Single Use Attachment Wraps
Reusable
Prior to using this sensor, the user should read and understand the Operator's Manual for the monitor and this
Directions for Use.
INDICATIONS
The RD SET™ YI Reusable Sensor is indicated for the continuous noninvasive monitoring of functional oxygen saturation of
arterial hemoglobin (SpO2) and pulse rate (measured by an SpO
patients during both no motion and motion conditions and for patients who are well or poorly perfused in hospitals, hospital-
type facilities, mobile, and home environments.
CONTRAINDICATIONS
The RD SET YI Multisite Reusable Sensor is contraindicated for patients who exhibit allergic reactions to foam urethane
products and/or adhesive tape.
DESCRIPTION
The RD SET YI sensor is applied to the sensor site using Masimo® attachment wraps. The attachment wraps are for single-
patient use only. The RD SET YI is for use only with devices containing Masimo SET® oximetry or licensed to use RD SET YI
sensors. The Masimo Attachment Wraps are for use only with the RD SET YI Reusable Multisite Sensors. Consult individual
instrument manufacturer for compatibility of particular instrument and sensor models. Each instrument manufacturer is
responsible for determining whether its instruments are compatible with each sensor model. The YI series has been verified
using Masimo SET Oximetry Technology.
The sensor must be removed and the site inspected at least every four (4) hours or sooner, and, if indicated by circulatory
condition or skin integrity, reapplied to a different monitoring site.
WARNING: Masimo sensors and cables are designed for use with devices containing Masimo SET® oximetry or licensed to
use Masimo sensors.
WARNINGS, CAUTIONS AND NOTES
• All sensors and cables are designed for use with specific monitors. Verify the compatibility of the monitor, cable and
sensor before use, otherwise degraded performance and/or patient injury can result.
• The sensor should be free of visible defects, discoloration and damage. If the sensor is discolored or damaged, discontinue
use.
• Never use a damaged sensor or one with exposed electrical circuitry.
• The site must be checked frequently or per clinical protocol to ensure adequate adhesion, circulation, skin integrity and
correct optical alignment.
• Exercise extreme caution with poorly perfused patients; skin erosion and pressure necrosis can be caused when the
sensor is not frequently moved. Assess site as frequently as every (1) hour with poorly perfused patients and move the
sensor if there are signs of tissue ischemia.
• Circulation distal to the sensor site should be checked routinely.
• During low perfusion, the sensor site needs to be assessed frequently for signs of tissue ischemia, which can lead to
pressure necrosis.
• With very low perfusion at the monitored site, the reading may read lower than core arterial oxygen saturation.
• Do not use tape to secure the sensor to the site; this can restrict blood flow and cause inaccurate readings. Use of
additional tape can cause skin damage, and/or pressure necrosis or damage the sensor.
• Carefully route cable and patient cable to reduce the possibility of patient entanglement or strangulation.
• Misapplied sensors or sensors that become partially dislodged may cause incorrect measurements.
• Misapplications due to wrong sensor types can cause inaccurate or no readings.
• Sensors applied too tightly or that become tight due to edema will cause inaccurate readings and can cause pressure
necrosis.
• Inaccurate SpO readings may be caused by abnormal venous pulsation or venous congestion.
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• Venous congestion may cause under reading of actual arterial oxygen saturation. Therefore, assure proper venous
outflow from monitored site. Sensor should not be below heart level (e.g. sensor on hand of a patient in a bed with arm
dangling to the floor, Trendelenburg position).
DIRECTIONS FOR USE
Not made with natural rubber latex
LATEX
PCX-2108A
02/13
sensor) for use with adult, pediatric, infant, and neonatal
2
5
en
Non-Sterile
9024C-eIFU-0518