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MAXN
Neonatal/Adult SpO
Identification of a substance that
is contained or present within the
product or packaging.
This product cannot be adequately cleaned and/or sterilized by the user in order to facilitate
safe reuse, and is therefore intended for single use. Attempts to clean or sterilize these
devices may result in bio-incompatibility, infection or product failure risks to the patient.
This device is not made with natural rubber latex or DEHP.
Directions for Use
Indications/Contraindications
The Nellcor™ Neonatal-Adult SpO
when continuous noninvasive arterial oxygen saturation and pulse rate monitoring are
required for neonates weighing less than 3 kg or adults weighing more than 40 kg.
The MAXN is contraindicated for use on patients who exhibit allergic reactions to the
adhesive tape.
Note: Adhesive sensor consists of sensor, cable and wrap adhesive flaps.
Instructions for Use
1.
Remove plastic backing from the MAXN and locate transparent windows on the adhesive
side. Windows cover optical components. Note corresponding alignment marks (a) on
nonadhesive side and dashed line (b) midway between the marks.
2.
Orient the MAXN so the dashed line is on the lateral edge of the site.
Neonates: The preferred site is a foot. Alternatively, use a hand. The window next to the
cable goes on the sole of the foot as shown.
Adults: The preferred site is an index finger. Alternatively, other fingers may be used. The
window next to the cable goes on the nail side, distal to the first joint. Do not place on a
joint. Note that the cable must be positioned on the top of the hand.
Note: When selecting a sensor site, priority should be given to an extremity free of an arterial
catheter, blood pressure cuff, or intravascular infusion line.
3.
Wrap the MAXN firmly, but not too tightly around the foot or finger. Windows must
oppose each other.
4.
Plug the MAXN into the oximeter and verify proper operation as described in the
oximeter operator's manual.
Note: If the sensor does not track the pulse reliably, it may be incorrectly positioned—or the
sensor site may be too thick, thin, or deeply pigmented, or otherwise deeply colored
(for example, as a result of externally applied coloring such as nail polish, dye, or
pigmented cream) to permit appropriate light transmission. If any of these situations
occurs, reposition the sensor or choose an alternate Nellcor sensor for use on a
different site.
To remove the Adhesive Sensor:
1.
Peel the tape wrap to gently remove the sensor.
2.
Disconnect the sensor from the monitor by unplugging the sensor from the extension
cable or monitor.
Reapplication
The MAXN can be reused on the same patient as long as the adhesive tape attaches without
slippage.
Sensor
2
Sensor, model MAXN, is indicated for single patient use
2
3
Identification of a substance that is
not contained or present within the
product or packaging.
2
1
3
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