NONIN 8008JFW Infant FlexiWrap Single Use Sensor Wrap Instruction Manual

NONIN 8008JFW Infant FlexiWrap Single Use Sensor Wrap

Product Information

Specifications

• Model: 8008JFW
• Intended Use: Single Use Sensor Wrap
• Designed for infants and neonates weighing 2 to 20 kilograms
• Application Site: Large toe of the right foot
• Indications: Extended duration monitoring where fingertip monitoring is impractical

Product Usage Instructions

Indications for Use
The Model 8008JFW Infant FlexiWrap is designed for extended duration monitoring on infants and neonates where fingertip monitoring is impractical.

FAQ (Frequently Asked Questions)
Q: Can the FlexiWrap be reused?
A: No, the FlexiWrap is designed for single-use only.

Q: What should I do if the sensor is damaged?
A: Discontinue use immediately and replace the sensor to avoid inaccurate readings or skin issues.

Instructions for Use-
Model 8008J Infant Flex Sensor and Model 8008JFW Infant FlexiWrap® Single Use Sensor Wrap

Indications for Use

Nonin’s Model 8008J Infant Flex Sensor is designed for extended-duration monitoring on the large toe or foot of infants and neonates weighing 2 to 20 kilograms, where fingertip monitoring is impractical and sensor motion may occur. The Nonin Model 8008JFW Infant FlexiWrap is designed for use with the Model 8008J Infant Flex Sensor. The preferred application site for infants is the large toe of the right foot. Other sites may not give acceptable results because of inadequate perfusion or light transmission.

CAUTION
Federal law (USA) restricts this device to sale by or on the order of a licensed practitioner

Clinical Benefits
Nonin pulse oximeters allow for the management of patients’ medical conditions by providing fast, accurate, real-time, noninvasive oxygen measurement in order to meet patients’ medical needs.

Warnings

• Do not use the device in an MR environment.
• Use only with Nonin pulse oximeters. These pulse oximeters are manufactured to meet the accuracy specifications for Nonin sensors. Using other pulse oximeters may cause improper sensor performance. Refer to Nonin pulse oximeter operator’s manuals for a complete listing of compatible oximeters, sensors, and accessories.
• Inspect the sensor application site at least every 4 hours to ensure correct sensor alignment and skin integrity. Patient sensitivity to sensors may vary due to medical status or skin condition.
• Avoid excessive pressure to the sensor application site as this may cause damage to the skin beneath the sensor.

Cautions

• To prevent improper performance and/or patient injury, verify sensor and pulse oximeter compatibility before use.

• Do not use a damaged sensor. If the sensor is damaged in any way,discontinue use immediately and replace the sensor.

• Discontinue use if the patient exhibits allergic reactions to the adhesive material.

• Do not stretch the adhesive tape while applying the sensor. This may cause inaccurate readings or skin blisters.

• Do not use caustic or abrasive cleaning agents on the sensors.

• Do not autoclave or immerse in liquid of any kind.

• Follow local governing ordinances and recycling instructions regarding disposal or recycling of the sensor and any components.

• A functional tester cannot be used to assess the accuracy of a pulse oximeter monitor or sensor.

• Refer to the pulse oximeter operator’s manual for additional warnings and cautions.

• Factors that may degrade pulse oximeter performance include the following:

  • excessive ambient light
    excessive motion

  • electrosurgical interference

  • arterial catheters, blood pressure cuffs, infusion lines, etc.

  • moisture in the sensor

  • improperly applied sensor

  • carboxyhemoglobin

  • methemoglobin

  • artificial nails

  • incorrect sensor type
    poor pulse quality

  • venous pulsations

  • anemia or low hemoglobin concentrations

  • cardiovascular dyes

  • sensor not at heart level

  • dysfunctional hemoglobin

  • fingernail polish

  • residue (e.g., dried blood, dirt, grease, oil) in the light path

Symbols

Applying the Infant FlexiWrap to the 8008J Infant Flex Sensor

1. Grasp the blue tab on the Infant FlexiWrap. Peel the paper backing halfway, as shown. Fold the unpeeled portion of the FlexiWrap back underneath the paper backing.
2. The Infant FlexiWrap has cutouts that match the shape of the Nonin Model 8008J Infant Flex Sensor. Carefully align the sensor with the cutouts on the adhesive side of the FlexiWrap, using the edge of the FlexiWrap as a guide. Then press the sensor firmly against the FlexiWrap.
3. Align the sensor cable with the notch in the FlexiWrap to stabilize  the cable.
4. Remove and discard the paper backing.

Attaching the FlexiWrap and Sensor

1. Place the FlexiWrap/Sensor assembly on the bottom of the large toe of the right foot. If impossible, position the sensor around the foot. (When placing the sensor on the foot, position the sensor as far forward near the toes as is practical. Place the light emitter portion on the top side of the foot, and the detector on the bottom.)
   Note: Sensor placement on the big toe is preferred, as this placement provides better light transmission than foot placement.

2. Use the center line mark (indicated by the black arrow in Figure 1) as a guide for aligning the light emitter and light detector. Ensure that the  light detector is centered on the bottom of the toe and the light emitter islocated directly opposite on the toe nail.

3. Wrap the FlexiWrap around the toe as indicated by the arrow in Figure

4. taking care to ensure that the detector and emitter remain aligned and directly opposite each other.

5. Fold the top flap down over the top of the toe, securing the FlexiWrap in place.

6. If necessary, re-align the sensor cable with the notch in the FlexiWrap.

7. Optional: For best results, secure the sensor cable independently from the sensor with medical tape. Ensure that the tape securing the cable does not restrict blood flow.

Note: If the sensor is not positioned properly, light might bypass the tissue and result in SpO2 inaccuracies. Proper sensor placement is critical for good performance.

Cleaning the Reusable Sensor

Cautions

• Clean the sensor before applying it to a new patient.
• Unplug the sensor from the pulse oximeter before cleaning.
• Do not sterilize, autoclave, or immerse the sensor in liquid of any kind.
• Do not pour or spray any liquids onto the sensor.
• Do not use caustic or abrasive cleaning agents on the sensor. Do not use cleaning agents containing ammonium chloride.

1. To clean the sensor, wipe all patient contact surfaces with a soft cloth dampened with a 10% bleach/90% water solution (household bleach [containing less than 10% sodium hypochlorite]).
2. Ensure that all tape residue is removed.
3. Allow the sensor to dry thoroughly before reusing.

Note: To minimize cable deterioration when cleaning the cable, gently wipe away from the plug end towards the sensor end.
The 8008JFW FlexiWrap sensor wrap is not reusable and is intended for single use only.

Specifications

SpO2 Accuracy: 1, 2, 3

SpO2

• Low Perfusion Accuracy: 70% to 100% ±2 digits (Arms*)1
• Pulse Rate Accuracy: 40 to 240 BPM ±3 digits (Arms*)1
• Pulse Rate Low Perfusion Accuracy: 40 to 240 BPM ±3 digits (Arms*)1
• Temperature: 4, 5
• Operating: -20 °C to 50 °C (-4 °F to 122 °F)
• Storage/Transportation: -40 °C to 70 °C (-40 °F to 158 °F)
• Humidity: 4, 5
• Operating: 10% to 95% non-condensing
• Storage/Transportation: 10% to 95% non-condensing
• • ±1 Arms encompasses 68% of the population at zero bias.

1. Additional accuracy and performance information can be found in the sensor accuracy document on the operator’s manual CD.
2. Accuracy testing was performed under no-motion conditions.
3. Accuracy specifications based on Nonin’s PureSAT® SpO2 technology and PureLight® sensor technology.
4. For combined oximeter/sensor specifications, refer to the applicable oximetry system’s operator’s manual.
5. Range as tested with Nonin’s PureSAT SpO2 technology.

Measurement Wavelengths and Output Power**
Red: 660 nanometers @ 3 mW nominal
Infrared: 910 nanometers @ 3 mW nominal
** This information is especially useful for clinicians.

Compliance
This product complies with ISO 10993-1.
Not made from natural rubber latex

Users and/or patients should report adverse events involving their Nonin device to Nonin Medical, Inc. and the competent authority of the EU Member State in which the user and/or patient is established, if applicable

Warranty

The 8008J is warranted for 90 days from delivery. The sensor’s expected service life is 90 days. Nonin reserves the right to make changes and improvements to these instructions and the product it describes at anytime, without notice or obligation.

www.nonin.com/warranty

Nonin Medical, Inc.
13700 1st Avenue North Plymouth, MN 55441, USA www.nonin.com

E-mail: info@nonin.com +1 763-553-9968 800-356-8874 (US and Canada)

Nonin Medical B. V. Doctor Paul Janssenweg 150 5026 RH Tilburg,
Netherlands Email: infointl@nonin.com (Europe) +31 (0)13 – 45 87 130 (Europe)

References

• Pulse and Regional Oximeters, Capnographs, Sensors | Nonin
• Warranty - Nonin

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