ADC Diagnostix 2100 Directions For Use Manual
Fingertip pulse oximeter
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Also See for Diagnostix 2100:
- Directions for use manual (15 pages) ,
- Directions for use (2 pages) ,
- Instructions for use (2 pages)
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Summary of Contents for ADC Diagnostix 2100
- Page 1 Diagnostix™ 2100 Fingertip ® Pulse Oximeter Directions for use ®...
- Page 2 ADC® Fingertip Pulse Oximeter Thank you for purchasing an DC Diagnostix Brand Fingertip 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 Pulse Oximeter will provide many years of dependable service.
- Page 3 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 con- stitute a diagnosis or medical advice of any kind.
- Page 4 Operating Instructions Be sure to insert two batteries before at- tempting to operate. Clean inside surface of oximeter and patient’ s finger with isopropyl alcohol before use. Squeeze the end opposite the power switch be- tween the thumb and forefinger in order to open the device (there is a textured surface on the bat- (Figure 2) tery cover side to facilitate grip).
- Page 5 Alarm On models equipped with an alarm, the alarm condition will appear when: SPO2 < 90% / PR <60 or >100bpm If the unit is in display mode 1 (silent mode), the parameter (SPO or PR) flashes and an audible beep is heard if it exceeds the alarm condition.
- Page 6 1. No battery or low battery 1. Replace battery. power. The monitor cannot be powered 2. Remove and reinstall battery. 2. Battery not installed correctly. 3. Contact customer service center. 3. The monitor may be damaged. 1. The Oximeter is automatically 1.
- Page 7 Guidance and Manufacturer’s Declaration - Electromagnetic Immunity For all Equipment and Systems that are not Life-Supporting Guidance and Manufacturer’ s declaration - electromagnetic environment specified below. The customer or the user of the PULSE OXIMETER should assure that it is used in such an environment. Immunity Compliance IEC 60601...
- Page 8 Technical Specifications Display Type: OLED Display SPO2 display range: 0-100% PR Display Range: 30-235 BPM PR Display Mode: Bargraph Data Update Time: < 15 s LED Wavelengths Red: 660nm Infrared: 940nm Measurement range: SPO2: 70-99% - 100% ±3%; s 70% no definition Pulse Rate: 30-235 BPM, ±2 bpm during the...
- Page 9 Symbol Definitions Symbol Definition Important Warning/Caution Latex-Free Equipment type is BF Hemoglobin Saturation Heart Rate (BPM) Low Power Indication Not for Continuous Monitoring Conforms to EU Standards uthorized European Represenative’ s Information Manufacturer’ s Information Serial Number 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 simu- lation pulse wave amplitude is at 6%.
- Page 10 To Obtain Warranty Service: Send item(s) postage paid to DC ® , ttn: Repair Dept., 55 Commerce Dr., Hauppauge, NY 11788. Please include your name and address, phone no., proof of purchase, and a brief note explaining the problem. Implied Warranty: ny implied warranty shall be limited in duration to the terms of this warranty and in no case beyond the original selling price (except where prohibited by law).
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