POE101-B

POE101-B

POE101-B

Product catalog summary
Device Overview: The POE101 Fingertip Pulse Oximeter is designed for measuring functional oxygen saturation (SpO2) and pulse rate in both adults and children. It is suitable for non-invasive spot checking and continuous monitoring in various environments, including home, professional care, and mobile settings. The device accommodates finger sizes between 0.8cm and 2.3cm.
Intended Use: The oximeter is intended for use in non-motion conditions and is not suitable for use in MRI or CT environments. It should be used in conjunction with other clinical assessments.
Device Features: The oximeter features a full-color OLED display, a 5-directional key for screen rotation and settings, and a micro-USB port for the POE101B model. It is powered by one AAA-size alkaline battery.
Setup and Operation: Users can adjust settings such as OLED brightness, initial timer, SpO2 and pulse rate alarm ranges, audio reminders, data recording intervals, and date & time. The device automatically turns on when a finger is inserted and off when removed. It includes a motion-tolerant algorithm to minimize motion artifacts.
Specifications: The device measures SpO2 in the range of 0% to 100% with a resolution of 1% and pulse rate from 30 to 250 bpm. It has an IPX2 rating for water resistance and complies with various international standards, including IEC and ISO.
Warnings and Cautions: The oximeter should not be used in explosive atmospheres or on patients with certain medical conditions without consulting a doctor. It is not an apnea monitor and should not be used as the sole method of patient assessment.
Cleaning and Maintenance: The device should be cleaned with a soft cloth dampened with mild detergent or isopropyl alcohol. High moisture environments should be avoided to prevent damage.
Troubleshooting: Common issues include low battery, incorrect finger placement, and electromagnetic interference. Solutions involve replacing the battery, repositioning the finger, and removing electronic devices that may cause interference.
Package Contents: The package includes the oximeter, user manual, quick reference card, warranty card, AAA battery, and USB cable (for POE101B).
Device Operation and Features: The document outlines the operation of a pulse oximeter, detailing steps for measuring SpO2 and pulse rate. The device updates readings with each pulse, and an audio beat can be generated if enabled. Alarm settings display SpO2 and pulse rate ranges, with specific delays for alarm conditions.
Specifications: The oximeter includes features such as auto on/off, data storage, and a USB port for the POE101B model. It is water-resistant and powered by batteries, with a specified usage life. Environmental conditions for operation include a temperature range of -30ºC to 70ºC, humidity from 15% to 90%, and atmospheric pressure from 700 hPa to 1013 hPa.
Maintenance and Safety: Users are advised to remove batteries if the device is unused for over a month and to store it under specified conditions. The document cautions against using caustic cleaning agents and emphasizes that repairs should be conducted by qualified personnel. It also provides guidelines for recycling and disposal.
Data Management: For the POE101B model, data can be retrieved via a USB connection, which switches the device to 'PC mode'. The document advises using the provided USB cable for safety and data quality.
Symbols and Terminology: The document explains symbols used on the device, such as %SpO2 for oxygen saturation, BPM for pulse rate, and icons indicating battery status, audio settings, and data recording.
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Catalog excerpts

POE101-B-1

C€ Authorized representative EU Separate collection for electrical and electronic devices (WEEE) CE Marking Read instructions before use Memory Icon-Indicate data is recordin' (only for POE101BB SpO2 A Show SpO2 alarm range BPM Alari Show pulse rate alarm range Battery Icon Indicate the battery power. Turn "RED” , as in-sufficient. Percentage of oxygen saturation (SpO2) Pulse rate (BPM) pO2 waveform POE101 includes the following items: A. Fingertip Pulse Oximeter, 1 unit B. User Manual, 1 sheet C. Quick reference card, , 1 piece D. Warranty Card, 1 piece E. AAA-Size Alkaline Battery, 1 piece F. USB cable, 1 piece (for POE101B only) Please make sure all items are packed. All items are non-sterile. If any item missing or damaged, contact your distributor. ► Setup the Device The device allows user to setup the 1) OLED brightness, 2)initial timer option, 3) SpO2 & pulse rate alarm range, 4) audio reminder, 5) data recording interval, 6) date & time and 7) factory default by LONG pressing the Q key. The setting mode can be entered either when the device is off or under operation._ A CAUTION! Tip® Key right to enter a sub-menu. For exit, tip it left at "Exit " selection. Under adjustment menu, tip Q Key right or left Slype BF not defibrillator proof A Caution; consult accompanying documents Do not use if package is damaged Serial number IPX2 Resistant to liquid ingress A CAUTION! • This oximeter is not an apnea monitor. • Significant levels of dysfunctional hemoglobin such as carbonxyhemoglobin to increase or decrease value, or change selection and press down for confirmation. Timer Alarm Beat Record POE101 is intended for measuring functional oxygen saturation of arterial hemoglobin (SpO2) and pulse rate for both adults and children as non-invasive spot checking and continuous monitoring in home and professional caring environment, and transport and mobile environment. It is designed for fingers between 0.8cm and 2.3cm (0.3 inch ~ 0.9 inch) and for patients during no-motion condition. ► physiological Principle POE101 determines SpO2 by measuring the absorption of red & infrared light passing through perfused tissue. Changes in absorption caused by the pulsation of blood in the vascular bed are used to determine SpO2 reading and pulse rate. ^Data Update and Signal Processing POE101 in the algorithms automatically extends the amount of data required for measuring SpO2 and pulse rate • Do not use the oximeter in an MRI or CT environment. • The oximeter is intended as an adjunct in subject assessment. It must be used in conjugation with other methods to assess clinical signs and symptoms. • Do not use the oximeter in an explosive atmosphere to avoid explosion hazard. • If the monitoring sites have trauma, disability or other medical conditions, users should consult doctors before use. • The oximeter has to measure the pulse properly to obtain accurate SpO2 reading. Blood flow restrictors (e.g., blood pressure cuffs) may hinder pulse measurements. Remove any objects that may hinder the performance of the oximeter. • Please do not leave the device to a child and always keep the battery cover in attach to avoid swallowing by a child. • Federal law (USA) restricts this device to sale by or on the order of a physician. or methemoglobin may affect the accuracy of the measurement. • Cardio green and intravascular dyes may affect the accuracy of POE101. • The performance of the oximeter might be affected by the presence of a defibrillator. • The oximeter may not work on all subjects. If you are unable to achieve stable readings, please discontinue use. • The oximeter has motion tolerant algorism to minimize the possible motion artifact. However, the oximeter may be still interpreted by motion. Please minimize subject motion as much as possible. • All the materials of the oximeter in contact with a patient or a user have passed ISO10993 Biological evaluation of medical devices accordingly. It shall be no toxicity harm to children, pregnant or nursing women. ► First Time Use For the first time use, a protective plastic membrane is attached to the front panel the sub-menu, please select among level 1~4 to adjust OLED brightness. Level 4 is the brightest and level 1 is the lowest. Please select higher level for high ambient light environment and lower level for power conservation. press down for confirmation.

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POE101-B-2

1. POE101 can be operated by either a patient or a trained personnel. Consult healthcare professionals before use. 2. The oximeter might not work on cold extremities due to poor circulation. Please warm or rub the finger , or reposition the device to improve it. 3. Check the applied site of a patient frequently to evaluate body circulation and skin sensitivity. The recommended maximum applied time at a single spot is 4 hours. Misapplication of the oximeter on applied site with excessive pressure for prolonged periods can introduce pressure injury. STEP1. Open up the oximeter and put one of your...

 Open the catalog to page 2

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