ADC Diagnostix™ 2150 Pediatric Fingertip Pulse Oximeter ® Directions for Use ®
ADC® Fingertip Pediatric Pulse Oximeter Thank you for purchasing an ADC Diagnostix™ Brand Fingertip Pediatric Pulse Oximeter. We’re proud of the care and quality that goes into the manufacture of every product that bears our name. With proper care and maintenance your Diagnostix™ Fingertip Pediatric Pulse Oximeter will provide many years of dependable service. Device Description and Intended Use This device is intended for medical diagnostic purposes only.
WARNING: Follow local ordinances and recycling instructions regarding disposal or recycling of the device and device components, including batteries. WARNING: This product may contain a chemical known to the state of California to cause cancer, birth defects, or other reproductive harm. CAUTION: Do not use the pulse oximeter in an explosive atmosphere. CAUTION: SpO2 and pulse rate data is displayed for informational purposes only and does not constitute a diagnosis or medical advice of any kind.
Operating Instructions 1. Be sure to insert two AAA batteries before attempting to operate. 2. Clean inside surface of oximeter and patient’s finger with 70% isopropyl alcohol before use. 3. Squeeze the end opposite the power switch between the thumb and forefinger in order to open the device (there is a textured surface on the battery cover side to facilitate grip) (Fig 2) 4. Insert patient’s finger, nail side up into the device.
Changing the Display Brightness (10 adjustable brightness settings) To change the brightness setting: After the unit is powered on, depress and hold the power switch (for 2 seconds), the brightness will then change by degrees. There are 10 levels of brightness. Note: The default setting is level 4. Lanyard Attachment 1. Thread thinner end of the lanyard through the hanging hole at either side of the device. 2. Thread thicker end of the lanyard through the threaded end before pulling it tightly.
“Err 3” or “Err 4” 1. Low Power. 1. Change batteries. 2. Recieving tube being shielded or dam- 2. Return to Service Center aged together with broken connector. 3. Mechanical Misplace for recieveemission tube. 4. Amp Circuit malfunction “Err 7” 1. Low Power 1. Change batteries. 2. Emission tube damaged 2. Return to Service Center 3. Current control circuit malfunction Guidance and Manufacturer’s Declaration Electromagnetic Emissions Guidance and Manufacturer’s declaration - electromagnetic emission.
Not for Continuous Monitoring Conforms to EU Standards Manufacturer’s Information Serial Number Authorized European Represenative’s Information Declaration: EMC of this product comply with IEC60601-1-2 standard. Measurement Performance in Low Perfusion Condition: required the test equipment (BIO-TEK INDEX Pulse Oximeter tester) the pulse wave is available without failure when the simulation pulse wave amplitude is at 6%.
