COVIDIEN DS100A Nellcor Adult SpO2 Sensor Reusable Instructions

COVIDIEN DS100A Nellcor Adult SpO2 Sensor Reusable

Adult SpO2 Sensor Reusable

Identification of a substance that is contained or present within the product or packaging.

Identification of a substance that is not contained or present within the product or packaging.

Protected against access to hazard-ous parts with a finger and protected against vertically falling water drops when sensor tilted up to 15°.

This device is not made with natural rubber latex or DEHP.

Directions for Use

Indications/Contraindications
The Nellcor™ Adult SpO2 Sensor, model DS100A, is indicated for use when continuous noninvasive arterial oxygen saturation and pulse rate monitoring are required for patients weighing greater than 40 kg.
The DS100A is contraindicated for use on active patients or for prolonged use. It is not designed for long-term monitoring. It must be moved every 4 hours (or more often, if indicated by circulatory status and/or skin integrity) and reapplied to a different site. If long-term monitoring is required, use an OxiMax™ oxygen sensor (MAXA, MAXAL, or MAXN) or an Oxisensor II sensor (D25, D25L, or N25), depending on patient age and size, and instrument compatibility.

Instructions for Use
Use this sensor only with Nellcor instruments and instruments containing Nellcor oximetry,
or with instruments licensed to use Nellcor sensors (Nellcor-compatible instruments). This sensor integrates Nellcor OxiMax technology into its design. When connected to an OxiMax-enabled instrument, this sensor uses OxiMax technology to provide additional advanced sensor performance features. Consult individual manufacturers for features and compatibility of particular instruments and sensor models.
Reusable sensors may be used on the same site for a maximum of 4 hours, provided the site is inspected routinely to ensure skin integrity and correct positioning. Because individual skin condition affects the ability of the skin to tolerate sensor placement, it may be necessary to change the sensor site more frequently with some patients.

To apply the DS100A:

1. Place an index finger over the sensor window of the DS100A with the finger tip against the stop. (1)

2. If the fingernail is long, the nail tip will extend over the finger stop. (2)

3. Spread open the rear tabs of the sensor to provide even force over the length of the pads. Check the position of the sensor. If an index finger cannot be positioned correctly, or is not available, a smaller finger can be used, or use an OxiMax™ or an Oxisensor II oxygen sensor. Do not use the DS100A on a thumb or toe or across a child’s hand or foot. (3)
   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.

4. The sensor should be oriented in such a way that the cable is positioned along the top of the hand. (4)

5. Plug the DS100A 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.

Cleaning

The DS100A may be surface-cleaned by wiping it with a solution such as 70% isopropyl alcohol. If low-level disinfection is required, use a 1:10 bleach solution. 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.

WARNINGS: If the sensor is misapplied with excessive pressure for prolonged periods, a pressure injury can occur.
CAUTION: Do not expose connector pins to cleaning solution as this may damage the sensor.

To clean or disinfect the sensor:

1. Saturate a clean, dry gauze pad with the cleaning solution. Wipe all surfaces of the sensor and cable with this gauze pad.
2. Saturate another clean, dry gauze pad with sterile or distilled water. Wipe all surfaces of the sensor and cable with this gauze pad.
3. Dry the sensor and cable by wiping all surfaces with a clean, dry gauze pad.

CAUTIONS

1. Do not sterilize by irradiation, steam, or ethylene oxide. Such sterilization could damage the sensor.
2. Failure to apply the DS100A properly may cause incorrect measurements.
3. Using the DS100A in the presence of bright lights may result in inaccurate measurements. In such cases, cover the sensor site with an opaque material.
4. Reusable sensors must be moved to a new site at least every 4 hours. Because individual skin condition affects the ability of the skin to tolerate sensor placement, it may be necessary to change the sensor site more frequently with some patients. If skin integrity changes, move the sensor to another site.
5. Intravascular dyes or externally applied coloring such as nail polish, dye, or pigmented cream, may lead to inaccurate measurements.
6. The performance of the DS100A is compromised by motion.
7. Do not apply tape to secure the sensor in place or to tape it shut; venous pulsations may lead to inaccurate saturation measurements.
8. As with all medical equipment, carefully route cables to reduce the possibility of patient entanglement or strangulation.
9. Do not use the DS100A or other oximetry sensors during MRI scanning. Conducted current may cause burns. Also, the DS100A may affect the MRI image, and the MRI unit may affect the accuracy of oximetry measurements.
10. Do not alter or modify the DS100A. Alterations or modifications may affect performance or accuracy.

If you have questions regarding any of this information, contact Covidien’s Technical Services Department, or your local Covidien representative.

Warranty
To obtain information about a warranty, if any, for this product, contact Covidien’s Technical Services Department, or your local Covidien representative.

Accuracy Specifications
For the accuracy specification range when used with Nellcor™ monitors, refer to information provided with the monitor, or (in the U.S.), contact Covidien’s Technical Services Department. Outside the U.S., contact your local Covidien representative.

For the accuracy specification range when used with a monitor other than those manufactured by Covidien, consult the information provided by the manufacturer of that instrument.

Note: Refer to the instrument operator’s manual for complete instructions for use of the sensor with that monitor.

Part No. 10051344 Rev D 2015-03
COVIDIEN, COVIDIEN with logo and Covidien logo are U.S. and internationally registered trademarks of Covidien AG.
Other brands are trademarks of a Covidien company.

© 2011 Covidien.
Covidien llc, 15 Hampshire Street, Mansfield, MA 02048 USA.
Covidien Ireland Limited, IDA Business & Technology Park, Tullamore.
www.covidien.com

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