Nonin Medical SABER SABER User Manual Model 3150 WristOx2 Pulse Oximeter

Nonin Medical, Inc. SABER Model 3150 WristOx2 Pulse Oximeter

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Operator’s ManualModel 3150 WristOx2™ Pulse OximeterWrist-Worn Pulse Oximeter with Bluetooth® Wireless TechnologyEnglish0123

iContentsIndications for Use.................................................................................................... 1Contraindications.................................................................................................... 1Warnings ................................................................................................................ 1Cautions ................................................................................................................. 2Declaration of Conformity with FCC and Canadian Ministry of Health Rules for Electromagnetic Compatibility .............................................. 3Federal Communications Commission (FCC) Notice............................................. 3Guide to Symbols...................................................................................................... 4Displays, Controls, and Indicators.......................................................................... 5Introduction ............................................................................................................... 8Unpacking the WristOx2, Model 3150 .................................................................... 8Standard Kit ....................................................................................................... 8Starter Kit .......................................................................................................... 8Batteries ................................................................................................................ 9Bluetooth Technology............................................................................................ 9Operation Modes..................................................................................................... 10Cable ................................................................................................................... 10Standby .............................................................................................................. 10On........................................................................................................................ 10Spot Check Mode ............................................................................................ 10Sensor Activation Mode................................................................................... 11Programmed Mode .......................................................................................... 11Using the WristOx2, Model 3150 ............................................................................ 12Installing Batteries ............................................................................................... 12Wrist Straps......................................................................................................... 13Ring Strap Description..................................................................................... 13Attach Ring Strap to Device............................................................................. 14Adjustable Strap Description............................................................................ 15Attach Adjustable Strap to Device ................................................................... 15Attaching the Sensor ........................................................................................... 18Patient Application............................................................................................... 19Two-Piece Wrist Band Application................................................................... 19Single Strap Application................................................................................... 21Verifying Operation.............................................................................................. 24Startup Sequence and Self-Test....................................................................... 24Activation Switch ................................................................................................. 25Activate Bluetooth Radio.................................................................................. 25Activate Device ................................................................................................ 25Error Codes ......................................................................................................... 25Troubleshooting..................................................................................................... 26Care and Maintenance ............................................................................................ 28Cleaning the Device ............................................................................................ 28Cleaning the Sensor............................................................................................ 28Cleaning the Wrist Band...................................................................................... 28Storing ................................................................................................................. 28

iiContents (Continued)Memory and Data.....................................................................................................29nVISION Software ....................................................................................................30nVISION Settings................................................................................................. 30Accessing nVISION Settings ............................................................................ 30Cable Connection................................................................................................. 31USB Driver Installation (XP) ............................................................................. 32USB Driver Installation (Vista) .......................................................................... 32USB Driver Installation (Windows 7)................................................................. 33Bluetooth Connection........................................................................................... 33Parts and Accessories ........................................................................................... 35Service, Support, and Warranty ............................................................................ 36Service and Support............................................................................................. 36Warranty............................................................................................................... 36Technical Information............................................................................................. 37Manufacturer’s Declaration ................................................................................ 37Equipment Response Time................................................................................ 40Testing Summary............................................................................................... 41SpO2 Accuracy Testing .................................................................................. 41Pulse Rate Motion Testing.............................................................................. 41Low Perfusion Testing .................................................................................... 41Specifications..................................................................................................... 42Oximeter Specifications.................................................................................. 42System Specifications..................................................................................... 43Transmitter ..................................................................................................... 44

iiiFiguresFigure 1. Front Display (Startup Screen).............................................................. 5Figure 2. Comparison of Full and Partial Display................................................ 11Figure 3. Remove Battery Door.......................................................................... 12Figure 4. Insert Batteries.................................................................................... 12Figure 5. Ring Strap ........................................................................................... 13Figure 6. Thread Ring Strap............................................................................... 14Figure 7. Attach Ring Strap................................................................................ 14Figure 8. Adjustable Strap.................................................................................. 15Figure 9. Thread Adjustable Wrist Strap ............................................................ 16Figure 10. Attach Adjustable Wrist Strap ........................................................... 16Figure 11. Device with Wrist Straps Attached (Front and Back Views).............. 17Figure 12. Attach Sensor.................................................................................... 18Figure 13. Verify Two-Piece Wrist Band Attachment ......................................... 19Figure 14. Thread and Tighten Two-Piece Wrist Band ...................................... 20Figure 15. Fasten Two-Piece Wrist Band........................................................... 20Figure 16. Apply Sensor to Patient .................................................................... 21Figure 17. Verify Single Strap Attachment ......................................................... 21Figure 18. Thread Single Strap ......................................................................... 22Figure 19. Tighten Single Strap.......................................................................... 22Figure 20. Fasten Single Strap........................................................................... 23Figure 21. Apply Sensor to Patient..................................................................... 23Figure 22. nVISION Settings Window ................................................................. 31TablesTable 1. Labeling Symbols.................................................................................. 4Table 2. Error Codes......................................................................................... 25Table 3. Electromagnetic Emissions ................................................................. 37Table 4. Electromagnetic Immunity................................................................... 38Table 5. Guidance and Manufacturer’s Declaration—Electromagnetic Immunity ................................................................ 39Table 6. Recommended Separation Distances................................................. 40

1Indications for UseIndications for UseThe Nonin Model 3150, WristOx2™ Pulse Oximeter is a small, wrist-worn device indicated for use in measuring, displaying, and storing functional oxygen saturation of arterial hemoglobin (%SpO2) and pulse rate of adult and pediatric patients. It is intended for spot-checking and/or data collection and recording of patients during both no motion and motion conditions, and for patients who are well or poorly perfused. The intended use environments are sleep and pulmonary rehab labs, surgical recovery, critical care, emergency room, long-term care, home use, and mobile units. ContraindicationsDo not use this device in a Magnetic Resonance (MR) environment or in the presence of flammable anesthetics or gases.This device is not defibrillation proof per IEC 60601-1:1988/A2:1995 clause 17h.Warnings This device is intended only as an adjunct device in patient assessment. It must be used in conjunction with other methods of assessing clinical signs and symptoms.Carefully route patient cables and connections to reduce the possibility of patient entanglement or strangulation.Use only Nonin-branded PureLight® pulse oximeter sensors. These sensors are manufactured to meet the accuracy specifications for Nonin pulse oximeters. Using other manufacturers’ sensors can result in improper pulse oximeter performance.This device is a precision electronic instrument and must be repaired by qualified technical professionals. Field repair of this device is not possible. Except to replace batteries, do not attempt to open the case or repair the electronics. Opening the case may damage the device and void the warranty.The USB cable must be unplugged from the device before replacing batteries. This device should not be used adjacent to or stacked with other equipment. If adjacent or stacked use is necessary, the device should be observed carefully to verify normal operation.The use of accessories, sensors, and cables other than those listed in this manual may result in increased electromagnetic emission and/or decreased immunity of this device.Do not use the device when alarms are required.Do not use a damaged sensor.This equipment complies with International IEC 60601-1-2:2007 for electromagnetic compatibility for medical electrical equipment and/or systems. This standard is designed to provide reasonable protection against harmful interference in a typical medical installation. However, because of the proliferation of radio-frequency transmitting equipment and other sources of electrical noise in healthcare and other environments, it is possible that high levels of such interference due to close proximity or strength of a source might disrupt the performance of this device. Medical electrical equipment needs special precautions regarding EMC, and all equipment must be installed and put into service according to the EMC information specified in this manual.Only use Nonin-branded sensors with a length of 1 meter or less. Accuracy may degrade if sensor cable is over 1 meter in length. Using the sensor cable adapter does not affect accuracy.

2Indications for UseCautions If this device fails to respond as described, refer to “Troubleshooting” or discontinue use until the situation has been corrected. Contact Nonin Technical Service.This device has motion tolerant software that minimizes the likelihood of motion artifact being misinterpreted as good pulse quality. In some circumstances, however, the device may still interpret motion as good pulse quality.Check the pulse oximeter sensor application site every 6-8 hours to determine the positioning of the sensor and the circulation and skin sensitivity of the patient. Patient sensitivity varies depending on medical status or skin condition.Do not place liquids on top of this device.Do not place the WristOx2, Model 3150, in liquid or clean it with agents containing ammonium chloride or isopropyl alcohol. Refer to the “Care and Maintenance” section of this operator’s manual. Use a detergent that is safe for skin and washable surfaces. Most detergents can be high sudsing, so use sparingly. Wipe with a damp, detergent free cloth to remove residue. Follow local, state, and national governing ordinances and recycling instructions regarding disposal or recycling of the device and device components, including batteries.In compliance with the European Directive on Waste Electrical and Electronic Equipment (WEEE) 2002/96/EC, do not dispose of this product as unsorted municipal waste. This device contains WEEE materials; please contact your distributor regarding take-back or recycling of the device. If you are unsure how to reach your distributor, please call Nonin for your distributor’s contact information.This device is designed to determine the percentage of arterial oxygen saturation of functional hemoglobin. Factors that may degrade pulse oximeter performance or affect the accuracy of the measurement include the following:• excessive ambient light• excessive motion• electrosurgical interference• blood flow restrictors (arterial catheters, blood pressure cuffs, infusion lines, etc.)• moisture in the sensor• improperly applied sensor• incorrect sensor typeDo not perform any testing or maintenance on this device while it is being used to monitor a patient.Verify all visible indicators appear during the start-up (initialization) sequence. If any indicator does not appear, do not use the device. Contact Nonin Technical Service for assistance.Portable and mobile RF communications equipment can affect medical electrical equipment.Batteries may leak or explode if used or disposed of improperly. Remove batteries if the device will be stored for more than 30 days. Do not use different types of batteries at the same time. Do not mix fully charged and partially charged batteries at the same time. These actions may cause the batteries to leak.To avoid the risk of confusing or misinterpreting patient data when transmitting data via Bluetooth, verify the device is paired with the correct display unit. The pulse oximeter may not work when circulation is reduced. Warm or rub the finger or reposition the sensor.A functional tester cannot be used to assess the accuracy of the oximeter or sensor.Do not fasten the device too tightly around the patient’s wrist. Inaccurate readings and patient discomfort could result. • poor pulse quality• venous pulsations• anemia or low hemoglobin concentrations• cardiogreen and other intravascular dyes• carboxyhemoglobin• methemoglobin• dysfunctional hemoglobin• artificial nails or fingernail polish

3Indications for UseDeclaration of Conformity with FCC and Canadian Ministry of Health Rules for Electromagnetic Compatibility • Nonin Medical, Inc., of 13700 1st Avenue North, Plymouth, Minnesota, 55441, declares under its sole responsibility that Model 3150, WristOx2 Pulse Oximeter, to which this declaration relates, complies with part 15 of the FCC Rules. Operation is subject to the following two conditions: (1) this device may not cause harmful interference, and (2) this device must accept any interference received, including interference that may cause undesired operation.• Ministry of Health (Canada), Safety Code 6: standards include a substantial safety margin designed to ensure the safety of all persons, regardless of age and health. The exposure standard for wireless mobile phones employs a unit of measurement known as the Specific Absorption Rate, or SAR. The SAR limit set by the FCC is 1.6 W/kg. Federal Communications Commission (FCC) Notice This device has been tested and found to comply with the limits for a class B digital device, pursuant to part 15 of the FCC Rules. These limits are designed to provide reasonable protection against harmful interference in a residential installation. This device generates, uses, and can radiate radio frequency energy. If not installed and used in accordance with the instructions, it may cause harmful interference to radio or television reception, which can be determined by turning the device off and on. The user is encouraged to try to correct the interference by one or more of the following measures: • Reorient or relocate the receiving antenna.• Increase the distance between the device and the receiver.• Connect the device to an outlet on a circuit different from the outlet where the receiver is connected• Consult the dealer or an experienced radio/TV technician for assistance.• RF Exposure: For body worn operation, to maintain compliance with FCC RF exposure guidelines, use only accessories that contain no metallic components. Use of other accessories may violate FCC RF exposure guidelines and should be avoided.• The WristOx2, Model 3150, is designed and manufactured not to exceed the emission limits for exposure to radio frequency (RF) energy set by the United States FCC. These limits are part of comprehensive guidelines and establish permitted levels of RF energy for the general population. The guidelines are based on the safety standards previously set by both U.S. and international standards bodies. This device has been shown to be compliant for localized specific absorption rate (SAR) for uncontrolled environment/general population exposure limits specified in ANSI/IEEE Std. C95.1-2005.• The FCC requires the user to be notified that any changes or modifications to this device that are not expressly approved by Nonin Medical, Inc. may void the user’s authority to operate the device.

4Guide to SymbolsGuide to SymbolsThis chapter describes the symbols that are found in this manual and on the WristOx2, Model 3150. Detailed information about display symbols can be found in “Displays, Controls, and Indicators.” Symbol Description!ECREP0123®Table 1: Labeling SymbolsCaution!Consult Instructions for Use. Authorized Representative in the European Community.CE Marking indicating conformance to EC directive No. 93/42/EEC concerning medical devices.Type BF-Applied Part (patient isolation from electrical shock)No alarmsIndicates separate collection for electrical and electronic equipment (WEEE).Continua Certified™ signifies that this product has been tested and proven to be interoperable with other products that carry the Continua Certified symbol.Bluetooth® figure markNon-ionizing electromagnetic radiation. Equipment includes RF transmitters. Interference may occur in the vicinity of equipment marked with this symbol.UL Mark for Canada and the United States with respect to electric shock, fire, and mechanical hazards only in accordance with UL 60601-1 and CAN/CSA C22.2 No. 601.1.IP33 Protected against spraying water and against access to hazardous parts with a tool, per IEC 60529.

Activation Switch Sensor Port 5Displays, Controls, and IndicatorsDisplays, Controls, and IndicatorsFigure 1: Front Display (Startup Screen) %SpO2 DisplayThis 3-digit display, located in the upper left corner of the LCD, shows percent blood oxygen saturation (%SpO2). The range is from 0 to 100 %. This display also shows the month, year, and hour (24-hour clock format) during startup. Pulse Rate DisplayThis 3-digit display, located below the %SpO2 display, shows the pulse rate in beats per minute (BPM). The range is from 18 to 321 BPM. This display also shows the day and minute during startup.

FullHalfCriticalLow6Displays, Controls, and IndicatorsActivation SwitchThis switch is located next to the sensor port. Pressing this switch activates the Bluetooth radio for 3 minutes. It can also be used to turn the device on when it is in Standby mode. See “Activation Switch” section for more information. Sensor Fault IndicatorThis indicator displays if the device determines a sensor fault exists (e.g., sensor disconnect, misalignment, or incompatibility with the device). It also displays when the finger is removed from the sensor.Pulse Strength Indicator This heart-shaped indicator is followed by up to nine curved bars. The heart shape is always visible, and the number of curved bars on the display depends on the pulse strength as determined by the oximeter.Poor Pulse Signal IndicatorThis indicator displays when the pulse signal is inadequate or the device does not sense a pulse. It may also display if there is excessive motion at the sensor site. Battery IndicatorThis indicator shows remaining battery life as either full, half, low, and critical (as shown at left). Replace the batteries when device reaches low state. When the battery reaches critical state, all indicators clear from the display except for the blinking critical battery indicator, the current session closes, and the Bluetooth radio shuts down.

8IntroductionIntroductionThe Bluetooth-enabled WristOx2, Model 3150, is a small, wrist-worn device that displays, measures, and stores patient SpO2 and pulse rate data. The device includes a Bluetooth radio with a range (spherical radius) of approximately 100 meters (328 feet). The device ships ready to use in Spot Check turn on mode. In Spot Check turn on mode, inserting a finger in the sensor automatically turns the device on. Approximately 10 seconds after the finger is removed, the device enters Standby mode. Advanced memory and programming features are available with Nonin’s nVISION® software (version 6.3 or greater). See the “nVISION Software” section to learn more about using the device with nVISION.Unpacking the WristOx2, Model 3150The WristOx2, Model 3150, standard or starter kit includes the items listed below. Once the shipping carton is unpacked, verify these items were received. Contact the carrier immediately if the shipping carton is damaged. Standard Kit• Model 3150, WristOx2 Pulse Oximeter• Model 8000SM-WO2, reusable soft sensor • 3 two-piece wrist bands, 1 each of the following:• 6 in. (15 cm)• 8 in. (20 cm)• 10 in. (25 cm)• 2 AAA (1.5 volt) alkaline batteries • Operator’s manual (CD)• USB driver software (on operator’s manual CD) – required to use the PC USB interface cable Starter KitA starter kit is required to configure the device and download data to a PC. The starter kit consists of the standard kit, plus:• 9 pack of two-piece wrist bands, 3 each of the following: • 6 in. (15 cm)• 8 in. (20 cm)• 10 in. (25 cm)• nVISION SpO2 data management software (CD)• PC USB interface cable

9IntroductionBatteriesThe device uses 2 AAA alkaline batteries. With new alkaline batteries, battery life is approximately 48 hours (minimum) when not connected to a Bluetooth device. When connected to a Bluetooth device, battery life will vary depending on class of operation. See “Specifications” for detailed battery life information.The battery indicator shows one of four states: full, half, low, and critical. Replace the batteries when device reaches low state. A low battery has a minimum of 10 minutes before it reaches critical state. Actual battery life depends on Bluetooth radio use. In critical battery mode, the battery indicator blinks and the device no longer monitors or records patient data. When batteries are removed, the device maintains the time and date for up to 30 seconds. If replacing batteries takes more than 30 seconds, or if the battery level is at or below the critical level, clock settings are lost and the device reverts to Spot Check mode. Use nVISION software to reset the clock and change the operation mode. Remove the batteries and disconnect the sensor if the device is to be stored for more than 1 month. In storage, battery life is approximately 9 months.Bluetooth TechnologyBluetooth technology allows wireless connections between electronic communications and computing devices. The technology is based on a radio link that offers fast and reliable data transmissions. Bluetooth uses a license-free, globally available frequency range in the ISM band—intended to ensure communication compatibility worldwide.Nonin’s use of Bluetooth wireless technology allows SpO2 and pulse rate data to be transmitted through a Bluetooth radio to a compatible Bluetooth-enabled device. Nonin’s wireless system removes the cable connection from the device, giving patients increased ability to move freely. To make efficient use of battery life, Nonin’s WristOx2, Model 3150, uses an automatically switchable Class 1/Class 2 Bluetooth radio with a maximum range (spherical radius) of about 100 meters (328 feet). Obstacles and other conditions may affect range, and class of operation and connection mode will impact battery life. See “Specifications” for detailed battery life information. NOTES:• This device contains non-volatile memory. Removing or replacing batteries does not affect the data stored in memory. Stored data remains in memory until overwritten by newer data or cleared from memory with nVISION software (version 6.3 or greater).• If batteries are replaced while recording data, the session will terminate and some data from the session may not be saved. The terminated session will be time stamped with the current date/time the next time the device turns on. • If clock settings are lost, the date and time restarts at 01:01:10:00:00.

10Operation ModesOperation ModesThe WristOx2, Model 3150, has three states: Cable, Standby, and On.Cable The device is in Cable mode when it is connected to a PC using the USB interface cable. While in Cable mode, the device does not collect or save data and the Bluetooth radio is off. Standby When the device is in Standby mode, the screen is blank and the device appears to be off. In Standby, it is ready for a signal that will turn the device on (e.g., pressing activation switch, inserting finger in sensor [Spot Check mode], connecting sensor [Sensor Activation mode], or programmed start time [Programmed mode]). While in Standby mode, the device does not collect or save data and the Bluetooth radio is off. OnWhen the device is on, it can collect and save data. The device features three turn on modes: • Spot Check mode• Sensor Activation mode• Programmed modeThe device is delivered in Spot Check mode. nVISION software (version 6.3 or higher) is needed to access the device settings and change Spot Check mode to Sensor Activation or Programmed mode (see “nVISION Software”).The device recalls the active settings when the device is shut off and turned on again. Spot Check ModeSpot Check mode is the default turn on operation mode. The device automatically turns on when a finger is inserted into the sensor. It enters Standby mode 10 seconds after the finger is removed. If the sensor is disconnected, the device enters Standby mode immediately. In this mode, the sensor can be left connected to the device.NOTE: If the device determines that a sensor fault exists (a sensor failure, misalignment, or incompatibility with the device) or if a pulse oximeter sensor signal cannot be detected, the device enters Standby mode after 3 minutes.

11Operation ModesSensor Activation ModeSensor Activation mode may be selected through nVISION software. In this mode, the device turns on when the activation switch is pressed or when the sensor is disconnected and reconnected. This mode is useful when using a sensor that is not easily removed from the sensor site (e.g., disposable or wrap sensor). If the sensor is not used for at least 10 minutes or if an inadequate pulse signal is detected, the device automatically enters Standby mode. To turn the device on again, press the activation switch or disconnect and reconnect the sensor.This mode allows for Full or Partial display (see figure 2 for display comparison). When using Partial display, the SpO2 and pulse rate readings do not display. The user will only see the battery indicator and the animated pulse strength indicator.Full Display Partial DisplayFigure 2: Comparison of Full and Partial Display Programmed ModeProgrammed mode may be selected and setup through nVISION software. With the software, the user can program the device to start and stop for up to three sessions. Once programmed, the next start time displays on the LCD every 30 seconds in HH:MM format. A sensor must be connected for Programmed mode to function.If the programmed device is in Standby mode and the activation switch is pressed, the user activates the Bluetooth radio and the device for 3 minutes. During this time, the user is able to take and store measurements. After 3 minutes, the device returns to Standby mode. This mode allows for Full or Partial display (see figure 2 above for display comparison). When using Partial display, the SpO2 and pulse rate readings do not display. The user will only see the battery indicator and the animated pulse strength indicator.NOTE: The sensor does not need to be applied to a finger to turn the device on. NOTE: A programmed device reverts to Spot Check mode if the clock is not set or if the clock settings are lost when replacing the batteries.

12Using the WristOx2, Model 3150Using the WristOx2, Model 3150Installing Batteries1. Open the battery compartment by sliding the battery door off the back of the device (figure 3). Figure 3: Remove Battery Door2. Insert 2 new AAA alkaline batteries (figure 4). Battery orientation is shown inside the battery compartment. Figure 4: Insert Batteries3. Replace battery door by sliding it back into place. 4. Inserting batteries does not turn the device on. In Spot Check mode, the device turns on when a finger is inserted in the sensor. WARNING: Do not use the device when alarms are required.WARNING: The USB cable must be unplugged from the device before replacing batteries.NOTE: When batteries are removed, the device maintains the time and date for up to 30 seconds. If replacing batteries takes more than 30 seconds, or if the battery level is at or below the critical level, the operation mode reverts to Spot Check mode. Use nVISION software to reset the clock and change the operation mode.

13Using the WristOx2, Model 3150Wrist StrapsThe WristOx2, Model 3150, is designed to be applied to the patient’s wrist using a two-piece wrist band. The two-piece wrist band consists of a ring strap and an adjustable strap. For pediatrics and petite adults, the device may be applied using a single adjustable strap. The single adjustable strap is the longer of the two straps in the two-piece wrist band package. Straps have hook and loop fasteners on one side. The other side has a smooth, woven fabric. When the straps are attached to the device, the woven side should touch the patient’s skin. This section contains descriptions of the straps and instructions for attaching the straps to the device. See the “Patient Application” section for instructions on how to apply the device to the patient. Ring Strap DescriptionOne end of the ring strap has a plastic ring. The square end has a hook and loop fastener (figure 5). The square end attaches to the strap bar at the top of the device, by the sensor port(see “Attach Ring Strap to Device”). Attach this end to strap bar by sensor portFastenerHook and Loop SideWoven SideFigure 5: Ring Strap NOTE: A wrist strap has a maximum of 10 uses before replacement is required.

14Using the WristOx2, Model 3150Attach Ring Strap to Device1. Place device face down.2. Locate strap bar at top of device (by sensor port). 3. Position ring strap so hook and loop side of strap faces up. 4. Thread square end fastener through the strap bar by the sensor port. Start fromthe back of the device and thread it towards the front of the device (figure 6). .Strap bar at top of device (by sensor port)Figure 6: Thread Ring Strap5. Fold strap so fastener adheres to the strap (figure 7). Figure 7: Attach Ring Strap6. Continue to “Attach Adjustable Strap to Device.”

15Using the WristOx2, Model 3150Adjustable Strap DescriptionThis strap is part of the two-piece wrist band and may also be used to apply the device using a single strap. The adjustable strap is available in various lengths (see “Parts and Accessories”). It has hook and loop fasteners at both ends (figure 8). The square end attaches to the strap bar at the bottom of the device, by the battery door (see “Attach Adjustable Strap to Device” section). Hook and Loop SideWoven SideAttach square end to strap bar by battery doorRounded End FastenerSquare End FastenerFigure 8: Adjustable StrapAttach Adjustable Strap to Device1. Place device face down. 2. Locate strap bar at bottom of device (by battery door).3. Position adjustable strap so hook and loop side of strap faces up.

16Using the WristOx2, Model 31504. Thread square end fastener through the strap bar by the battery door. Start from the back of the device and thread it towards the front of the device (figure 9). Strap bar by battery doorFigure 9: Thread Adjustable Wrist Strap5. Fold square end of strap so square end fastener adheres to the strap (figure 10). Figure 10: Attach Adjustable Wrist Strap

17Using the WristOx2, Model 31506. Verify straps are attached properly (figure 11). The smooth, woven side of the strap should contact the patient.Front ViewBack View Figure 11: Device with Wrist Straps Attached (Front and Back Views)

19Using the WristOx2, Model 3150Patient ApplicationThe WristOx2, Model 3150, is usually worn on the back of a patient’s wrist. This section describes how to secure the device to a wrist using either the two-piece wrist band or a single strap. Two-Piece Wrist Band Application1. Verify the ring strap and the adjustable strap have been attached properly to the device (figure 13). If straps have not been attached to the device, see “Attach Ring Strap to Device” and “Attach Adjustable Strap to Device.”Back ViewFront ViewFigure 13: Verify Two-Piece Wrist Band AttachmentNOTE: Straps can be used to secure the device to an alternate location (e.g., the upper arm or a bed rail). See “Part and Accessories” for additional strap lengths. NOTE: Ensure the wrist band fits comfortably on the patient’s arm. Do not over-tighten the wrist band.

20Using the WristOx2, Model 31502. Place the device on the back of the patient’s arm. 3. Thread the rounded end of the adjustable strap through the plastic ring on the ring strap. Pull the adjustable strap through the plastic ring until the device fits comfortably on the wrist (figure 14). FastenerPlastic RingFigure 14: Thread and Tighten Two-Piece Wrist Band4. Fold the adjustable strap back over the plastic ring and attach the fastener to the adjustable strap (figure 15). Figure 15: Fasten Two-Piece Wrist Band5. Attach the sensor if it is not already connected (see “Attaching the Sensor”).6. Apply the sensor to the patient (figure 16). Refer to the sensor Instructions for Use for proper sensor application sites and sensor application cautions and warnings.

21Using the WristOx2, Model 3150Figure 16: Apply Sensor to Patient7. When in Spot Check mode, inserting a finger in the sensor automatically turns the device on. When the finger is removed, the device enters Standby mode in approximately 10 seconds.8. If the device does not turn on, verify battery orientation, operation mode, and sensor connection. Refer to “Troubleshooting” for additional information. Single Strap Application1. Verify the adjustable strap has been attached to the device by the battery door (figure 17). If strap has not been attached, see “Attach Adjustable Strap to Device.”Front ViewBack ViewFigure 17: Verify Single Strap Attachment NOTE: Depending on the sensor and ambient light conditions, it may take up to 3 minutes for the device to enter Standby mode. NOTE: Patients using a single strap may need assistance applying the device. NOTE: Ensure the wrist band fits comfortably on the patient’s arm. Do not over-tighten the wrist band.

22Using the WristOx2, Model 31502. Place the device on the back of the patient’s arm and wrap the strap around the patient’s arm. 3. Thread the rounded end of the strap through the strap bar by the sensor port (figure 18). Start from the back of the device and pull it towards the front of the device.Figure 18: Thread Single Strap4. Pull the strap through the strap bar until the device fits comfortably on the patient’s wrist (figure 19). Figure 19: Tighten Single Strap

24Using the WristOx2, Model 3150Verifying OperationWhen the WristOx2, Model 3150, first turns on, it performs a startup sequence and self-test. It occurs:• When a sensor is applied to a patient (Spot Check mode).• When a sensor is attached to the device (Sensor Activation mode).• At a programmed start time when a sensor is attached to the device (Programmed mode). • After the activation switch is pressed while the device is in Standby mode.• After the device disconnects from nVISION (Bluetooth connection only).Verify all indicators display during the startup sequence. Indicators appear in the following order for 1 second each.Startup Sequence and Self-TestIf the time is not set, the device displays 01:01:10:00:00. If any indicator does not display, do not use the device. Contact Nonin Technical Service for assistance. 1. r and the software revision level:2. All display icons: 3. Date/time using 24-hour clock format (MM:DD:YY:HH:MM) (example shows 23 April 2010 at 5:57 p.m.): Month and Day Year  (MM:DD) (YY) Hour and Minutes (HH:MM)

25Using the WristOx2, Model 3150Activation SwitchThe activation switch is located next to the sensor port at the top of the WristOx2, Model 3150. It is primarily used to:• Activate the Bluetooth radio when the device is either on or in Standby.• Activate the device when it is in Sensor Activation mode so the user does not need to disconnect and reconnect the sensor. It will also activate the device when it is in Spot Check and Programmed modes. Activate Bluetooth RadioWhen the device’s Bluetooth radio is on, a master device can connect to it. If a connection is not made, the Bluetooth radio shuts down. Pressing the activation switch turns the Bluetooth radio on for 3 minutes. The device will remain on until the Bluetooth radio shuts down. For example, if in Sensor Activation mode, unplugging the sensor will not put the device in Standby. Activate DeviceWhen in Sensor Activation mode, the device enters Standby mode after 10 minutes without a signal. Pressing the activation switch allows the user to turn the device on without disconnecting and reconnecting the sensor. Error CodesThis device includes error codes that indicate problems with the unit. When an error occurs, the device displays the letters “Er” and a two-digit code (table 2). Table 2: Error CodesSome error codes may be corrected by the user. See “Troubleshooting” for more information. Error Code Description01 Configuration sector error02 Patient data pointer error03 Main memory pointer error (Device memory is intact; however, the most recent session may be missing from the device.)04 Data format 13 stored packet pointer error05 Main data format 13 pointer error (Device memory is intact; however, the most recent stored measurement may be missing from the device.)

26TroubleshootingTroubleshootingProblem Possible Cause Possible SolutionDevice will not activate. Batteries inserted wrong. Check batteries.Batteries are depleted. Replace batteries.Sensor is disconnected. Reconnect sensor.Device is in Sensor Activation mode and has timed out. Press the activation switch.Disconnect and then reconnect the sensor.Device is in Programmed mode. Use nVISION software to select Spot Check or Sensor Activation mode.%SpO2 and pulse rate do not display. Device set in Partial Display mode. Use nVISION software to select Full Display mode. Reconnect sensor. Poor pulse signal indicator displays. Excessive patient motion. Reduce patient motion.Poor pulse signal indicator displays and pulse strength indicator shows two bars or less.Inadequate pulse signal. Reposition or replace sensor, or place sensor on a different finger.Remove and reconnect sensor. Hands are cold. Warm sensor application site.No pulse display on pulse strength bar graph indicator.Sensor applied incorrectly. Refer to sensor Instructions for Use for proper sensor application.Device needs repair. Contact Nonin Technical Service.Possible interference from blood flow restrictors (arterial catheters, blood pressure cuffs, infusion lines, etc.).Reduce or eliminate restriction.Reduced circulation due to excess pressure from sensor. Check sensor alignment, reposition sensor, verify correct sensor size.Excessive ambient light. Shield sensor from light source. Check sensor alignment.

27TroubleshootingIf these solutions do not correct the problem, please contact Nonin Technical Service at (800) 356-8874 (USA and Canada) or + 1 (763) 553-9968.No pulse display on pulse strength indicator (continued).Sensor applied to polished or artificial nail. Remove fingernail polish or an artificial nail.Sensor Light-Emitting Diode (LED) is not lit. Contact Nonin Technical Service. Er 01 displays on LCD. Device configuration memory failure. Device reverts to default settings (Spot-Check mode, 4-second sample rate). Use nVISION software to change settings. If error code continues, contact Nonin Technical Service. Er 02 or 04 displays on LCD. Device memory failure. Contact Nonin Technical Service. Er 03 or 05 displays on LCD. Device failure. Device memory intact, but device may have lost most recent session or stored data.If error code continues, contact Nonin Technical Service. Dashes continually display on LCD. Sensor malfunction. Replace sensor with a Nonin-branded sensor. Device does not record in Programmed mode.Data collection start and stop times are set incorrectly. Use nVISION software to program correct start and stop times.Clock settings are lost after replacing batteries. Use nVISION software to reset clock.Devices will not pair. Device is out of range. Verify device is in range while being paired (approximately 100 meters [328 feet] spherical radius).Bluetooth radio has timed out. Press activation switch to turn on Bluetooth radio.Problem Possible Cause Possible Solution

28Care and MaintenanceCare and MaintenanceThe device requires no calibration or maintenance other than battery replacement.Cleaning the DeviceWipe the device with a soft cloth dampened with a 10% bleach solution. Do not use undiluted bleach or any cleaning solution other than those recommended here, as permanent damage could result. Dry with a soft cloth, or allow to air dry. Clean once per week or more frequently if handled by multiple users. !CAUTION: Do not place the WristOx2, Model 3150, in liquid or clean it with agents containing ammonium chloride or isopropyl alcohol. Cleaning the SensorRefer to the sensor Instructions for Use for cleaning information.Cleaning the Wrist BandThe wrist band is designed for single-patient use and may be used up to 10 times. If it needs to be cleaned, hand wash with a mild detergent (see note) in cool water (30 °C/86 °F). Allow to air dry. Do not machine wash or dry. The wrist band will shrink if placed in a dryer. CAUTION: Use a detergent that is safe for skin and washable surfaces. Most detergents can be high sudsing, so use sparingly. Wipe with a damp, detergent free cloth to remove residue. StoringStore the device within the stated environmental specifications. See “Specifications” for additional information. Remove the batteries and disconnect the sensor if it is to be stored for more than 1 month. NOTE: Mild detergents, such as hand and dish washing liquid detergents, dissolve dirt and grease. To clean washable surfaces, use in a solution of warm water.

29Memory and DataMemory and Data The WristOx2, Model 3150 measures, collects, and stores up to 1,080 hours of SpO2 and pulse rate data with a 4-second data collection rate. Data collected at a 1 or 2-second rate reduces memory capacity to 270 or 540 hours, respectively. When the memory is full, the device overwrites the oldest existing data with the new data. Each time the device is turned on, data are automatically stored in memory. Data collection of less than 1 minute is not retained in memory. Each time the device turns on, the current oximeter time and date (if the clock is set properly) are stored in memory to allow quick differentiation of recording sessions. Patient SpO2 and pulse rate are stored every 4 seconds (default), or every 1 or 2 seconds if programmed using nVISION software. The oxygen saturation values are stored in 1% increments in the range of 0 to 100%.This device contains non-volatile memory. Removing or replacing batteries does not affect the data stored in memory. Stored data remains in memory until overwritten by newer data or cleared from memory with nVISION software.NOTE: Downloading data in memory does not clear memory. To clear memory, see “nVISION Settings.”

30nVISION SoftwarenVISION SoftwareNonin’s nVISION software (version 6.3 or greater) works with Microsoft Windows® 2000/XP/Vista/7 operating systems. It allows users to transfer recorded patient data from the device to a PC and then analyze, report, and archive the data. The software is required to access the device’s additional modes of operation and advanced features. nVISION SettingsThe following WristOx2, Model 3150, settings are programmed using nVISION:• Date and time – 24-hour clock format • Display options – allows clinicians to choose the best display option for each patient:• Full display shows %SpO2 and pulse rate data• Partial display shows pulse strength indicator, but not %SpO2 and pulse rate data• Patient data storage (sample) rate – 1, 2, or 4 seconds • Operation Modes – Sensor Activation, Spot Checking, and Programmed (see “Activation Options”)• Patient ID – up to 50 alphanumeric characters• Bluetooth Radio – disable at startup• Synchronize device time/date to the PC time/date • Download and save patient data to a PC • Clear device memoryTo access nVISION settings, connect the device to a PC using either the PC USB interface cable or a Bluetooth connection. Accessing nVISION Settings1. Connect the device to a PC using the USB interface cable (see “Cable Connection”) or Bluetooth (see “Bluetooth Connection”).2. Open nVISION.3. Click the Data Capture icon, or select New Data Capture from the File drop down menu. 4. Select 3150 from the list of oximeters.5. Click Settings.6. “Enter Wrist Oximeter Settings” window opens (figure 22). Update or change settings as needed. 7. Click OK.8. For more information, see nViSION Help.

31nVISION Software. Figure 22: nVISION Settings WindowCable ConnectionTo connect the device to a PC, use the PC USB interface cable found in the starter kit. Once connected to a PC, the device settings may be accessed and data can be downloaded using nVISION software. The USB driver software for the cable needs to be installed before the device can connect to the PC. The software is located in the USB Driver folder on the Operator’s Manual CD. 1. Install USB driver if needed. See appropriate “USB Driver Installation” section for more information. 2. Connect the cable to the USB port on the PC.3. Connect the cable to the device’s sensor port.

33nVISION SoftwareUSB Driver Installation (Vista) 1. Connect the USB cable to the sensor port on the device and a USB port on the PC. 2. In the Found New Hardware window, select Locate and install driver software (recommended).3. Windows needs your permission to continue pop up appears. Continue with installation. 4. The USB driver software is on the Operator’s Manual CD. Insert the CD into the PC’s CD-DVD drive and click Next. 5. Update Driver Software - Model 3150 window opens. Choose Browse my computer for driver software.6. Browse to the USB Driver folder on the Operator’s Manual CD and click OK. 7. Click Next. 8. In the Windows Security pop-up window, select Install this driver software anyway.9. Driver software installs. When Windows has successfully updated the driver software, click Close.10. Open the Device Manager by clicking Start / Control Panel / Device Manager.11. In the Device Manager window, look up the communications (comm or COM) port for the device. Expand Ports (COM & LPT). One port should say “Nonin Model 3150 (COM#).” Make a note of the COM#. It is needed to set up the device with nVISION.USB Driver Installation (Windows 7)1. The USB driver software is on the Operator’s Manual CD. Insert the CD into the PC’s CD-DVD drive. 2. Connect the USB cable to the sensor port on the device and a USB port on the PC.3. Open the Device Manager by clicking Start / Control Panel / System and then selecting Device Manager.4. Expand Other devices.5. Right click Model 3150 and select Update Driver Software...6. Update Driver Software - Model 3150 window opens. Choose Browse my computer for driver software.7. Browse to the USB Driver folder on the Operator’s Manual CD and click OK. 8. Click Next. 9. In the Windows Security pop-up window, select Install this driver software anyway.10. Driver software installs. When Windows has successfully updated the driver software, click Close.11. In the Device Manager window, look up the communications (comm or COM) port for the device. Expand Ports (COM & LPT). One port should say “Nonin Model 3150 (COM#).” Make a note of the COM#. It is needed to set up the device with nVISION.

34nVISION SoftwareBluetooth ConnectionBefore a Bluetooth master device can connect with the WristOx2, Model 3150 (slave device), the devices must be paired. Once paired, the WristOx2, Model 3150, will automatically connect with the last paired master device when turned on or activated.1. To connect the WristOx2, Model 3150, to a PC or another device using Bluetooth, see Nonin’s online Bluetooth Connection Tutorial: http://www.nonin.com/training/products/3150/bluetooth_connection_tutorial/2. When nVISION connects to the WristOx2, Model 3150, the device stops recording patient data and the following indicators display on the LCD:•CP • Battery indicator• Bluetooth icon with animated bars 3. For more information about nVISION, refer to nVISION Help.NOTE: Etched onto the device is the word “pin” followed by a 6-digit number. This is the device’s unique identification number, also known as the Bluetooth Passkey or PIN Code. This number is used when pairing the device to the host system. Refer to the host system’s operator’s manual for additional information.

35Parts and AccessoriesParts and AccessoriesFor more information about Nonin parts, accessories and sensors, contact your distributor, or contact Nonin at (800) 356-8874 (USA and Canada) or +1 (763) 553-9968. This information is also available on Nonin’s website: www.nonin.com. Model Number DescriptionReusable Pulse Oximeter Sensors3100CC Carrying Case 3150 Manual CD with Operator’s Manual and USB Driver Software3150SC PC USB Interface CablenVISION nVISION Software (version 6.3 or greater). Used with Microsoft Windows 2000/XP/Vista/7 operating systems.3150I Sensor Adapter Cable. Used to connect 1-meter, 9-pin connector sensors to the WristOx2, Model 3150. For compatible 1-meter sensors, contact Nonin, your distributor, or visit www.nonin.com. 3150WB Two-piece Wrist Band. Available lengths:6 in. (15 cm)8 in. (20 cm)10 in. (25 cm)13 in. (33 cm) 3150WBE Wrist Band Extender, 5 in. (13 cm) 8000AA-WO2 Adult Articulated Finger Clip Sensor 8000J-WO2 Adult Flex Sensor8000SS-WO2 Soft Sensor Small8000SM-WO2 Soft Sensor Medium8000SL-WO2 Soft Sensor Large

36Service, Support, and WarrantyService, Support, and WarrantyService and SupportFor information about the device and accessories, contact your local sales representative or distributor. For the sales representative or distributor in your area, contact Nonin. A return authorization number is required before returning any product to Nonin. To obtain this return authorization number, contact Nonin’s Technical Service Department at:Nonin Medical, Inc.13700 1st Avenue NorthPlymouth, Minnesota 55441-5443 USA(800) 356-8874 (USA and Canada) + 1 (763) 553-9968 Fax: + 1 (763) 553-7807E-mail: info@nonin.comwww.nonin.comWarrantyNONIN MEDICAL, INCORPORATED, (NONIN) warrants to the purchaser the Model 3150, WristOx2 Pulse Oximeter for 3 years from the date of purchase. NONIN shall repair or replace any WristOx2, Model 3150, found to be defective in accordance with this warranty, free of charge, for which NONIN has been notified by the purchaser by serial number that there is a defect, provided said notification occurs within the applicable warranty period. This warranty shall be the sole and exclusive remedy by the purchaser hereunder for any WristOx2, Model 3150, delivered to the purchaser that is found to be defective in any manner, whether such remedies be in contract, tort, or by law.This warranty excludes cost of delivery to and from NONIN. All repaired units shall be received by the purchaser at NONIN’s place of business. NONIN reserves the right to charge a fee for a warranty repair request on any unit found to be within specifications. The WristOx2, Model 3150, is a precision electronic instrument and must be repaired by knowledgeable and specially trained NONIN personnel only. Accordingly, any sign or evidence of opening the WristOx2, Model 3150, field service by non-NONIN personnel, tampering, or any kind of misuse of the WristOx2, Model 3150, shall void the warranty. All non-warranty work shall be performed according to NONIN standard rates and charges in effect at the time of delivery to NONIN.DISCLAIMER/EXCLUSIVITY OF WARRANTY:THE WARRANTIES IN THIS MANUAL ARE EXCLUSIVE, AND NO OTHER WARRANTIES OF ANY KIND, WHETHER STATUTORY, WRITTEN, ORAL, OR IMPLIED, SHALL APPLY.

37Technical InformationTechnical InformationManufacturer’s DeclarationRefer to the following table for specific information regarding this device’s compliance to IEC 60601-1-2. Emissions Test Compliance Electromagnetic Environment—GuidanceThis device is intended for use in the electromagnetic environment specified below. The customer and/or user of this device should ensure that it is used in such an environment.RF Emissions CISPR 11 Group 2 This device must emit electromagnetic energy in order to perform its intended function. Nearby electronic equipment may be affected. RF EmissionsCISPR 11 Class B This device is suitable for use in all establishments, including domestic and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes.Harmonic EmissionsIEC 61000-3-2N/AVoltage Fluctuations/Flicker EmissionsIEC 61000-3-3N/ATable 3: Electromagnetic Emissions

38Technical Information Immunity Test IEC 60601 Test Level Compliance Level Electromagnetic Environment—GuidanceThis device is intended for use in the electromagnetic environment specified below. The customer and/or user of this device should ensure that it is used in such an environment.Electrostatic Discharge (ESD)IEC 61000-4-2±6 kV contact±8 kV air ±6 kV contact±8 kV air Floors should be wood, concrete, or ceramic tile. If floors are covered with synthetic material, relative humidity should be at least 30%. Electrical Fast Transient/BurstIEC 61000-4-4±2 kV for power supply lines±1 kV for input/output linesN/A Mains power quality should be that of a typical commercial or hospital environment.Surge IEC 61000-4-5 ±1 kV differential mode±2 kV common mode N/A Mains power quality should be that of a typical commercial or hospital environment.Voltage dips, short interruptions, and voltage variations on power supply input linesIEC 61000-4-11±5% UT (>95% dip in UT) for 0.5 cycle±40% UT (60% dip in UT) for 5 cycles±70% UT (30% dip in UT) for 25 cycles<5% UT (>95% dip in UT) for 5 sec.N/A Mains power quality should be that of a typical commercial or hospital environment. Power Frequency(50/60 Hz) Magnetic FieldIEC 61000-4-83 A/m 3 A/m Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment.NOTE: UT is the AC mains voltage before application of the test level. Table 4: Electromagnetic Immunity

Immunity Test IEC 60601 Test Level Compliance Level Electromagnetic Environment—GuidanceThis device is intended for use in the electromagnetic environment specified below.The customer and/or user of this device should ensure that it is used in such an environment.Portable and mobile RF communications equipment should be used no closer to any part of the device, including cables, than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter.Recommended Separation DistanceConducted RFIEC 61000-4-6 3 Vrms150 kHz to 80 MHz3 Vrmsd1.17 P=Radiated RFIEC 61000-4-3 3 V/m80 MHz to 2.5 GHz3 V/m3 V/m80 kHz to 800 MHz d1.17 P=800 MHz to 2.5 GHz d2.33 P=where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer and d is the recommended separation distance in meters (m). Field strengths from fixed RF transmitters, as determined by an electromagnetic site surveya, should be less than the compliance level in each frequency range.bInterference may occur in the vicinity of equipment marked with the symbol: NOTES: 1. At 80 MHz and 800 MHz, the higher frequency range applies.2. These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people.a. Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile radios, amateur radio, AM and FM radio broadcast, and TV broadcast cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the device is used exceeds the applicable RF compliance level above, the device should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the device.b. Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.39Technical Information Table 5: Guidance and Manufacturer’s Declaration—Electromagnetic Immunity

40Technical Information This table details the recommended separation distances between portable and mobile RF communications equipment and this deviceThis device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. Users of this device can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communication equipment (transmitters) and the device as recommended below, according to maximum output power of the communications equipment.Separation Distance According to Frequency of TransmitterRated Maximum Output Power of Transmitter Wd1.17 P=150 kHz to 80 MHzd1.17 P=80 MHz to 800 MHzd2.33 P=800 MHz to 2.5 GHz0.01 0.12 0.12 0.230.1 0.37 0.37 0.7311.2 1.2 2.310 3.7 3.7 7.3100 12 12 23For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.NOTES: 1. At 80 MHz and 800 MHz, the higher frequency range applies. 2. These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption and reflection from structures, objects, and people. SpO2 Values Average LatencyPulse Rate Values Response LatencyEquipment Response TimeExample - SpO2 Exponential AveragingSpO2 decreases 0.75% per second (7.5% over 10 seconds)Pulse Rate = 75 BPMTable 6: Recommended Separation DistancesStandard/Fast Averaged SpO24 beat exponential 2 beatsStandard/Fast Averaged Pulse Rate 4 beat exponential 2 beats

60657075808590951000.08.016.024.032.040.048.056.064.072.080.0Time in secondsSpO2SaO2 Reference 4 Beat Average41Technical InformationSpecific to this example:• The response of the 4-beat average is 1.5 seconds.Testing SummarySpO2 accuracy and low perfusion testing was conducted by Nonin Medical, Inc., as described below.SpO2 Accuracy TestingSpO2 accuracy testing is conducted during induced hypoxia studies on healthy, non-smoking, light- to dark-skinned subjects during motion and no-motion conditions in an independent research laboratory. The measured arterial hemoglobin saturation value (SpO2) of the sensors is compared to arterial hemoglobin oxygen (SaO2) value, determined from blood samples with a laboratory co-oximeter. The accuracy of the sensors in comparison to the co-oximeter samples measured over the SpO2 range of 70 - 100%. Accuracy data is calculated using the root-mean-squared (Arms value) for all subjects, per ISO 9919:2005, Medical Electrical Equipment—Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use.Pulse Rate Motion TestingThis test measures pulse rate oximeter accuracy with motion artifact simulation introduced by a pulse oximeter tester. This test determines whether the oximeter meets the criteria of ISO 9919:2005 for pulse rate during simulated movement, tremor, and spike motions.Low Perfusion TestingThis test uses an SpO2 Simulator to provide a simulated pulse rate, with adjustable amplitude settings at various SpO2 levels for the oximeter to read. The oximeter must maintain accuracy in accordance with ISO 9919:2005 for heart rate and SpO2 at the lowest obtainable pulse amplitude (0.3% modulation).

42Technical InformationSpecificationsOximeter SpecificationsOxygen Saturation Display Range: 0 to 100 % SpO2Pulse Rate Display Range: 18 to 321 beats per minute (BPM)Displays:Numeric: 3-digit LCDPulse Strength: Pulse Strength Bar Graph Saturation Accuracy Armsa:a. ±1 Arms represents approximately 68% of measurements. 70 % to 100 %%SpO2: No Motion Motionbb. SpO2 accuracy in motion specified for 8000AA-W sensor.Low Perfusion8000AA-WO2: ±2 units ±2 units ±2 units8000J-WO2: ±3 units NA ±2 units8000SM-WO2: ±2 units NA ±2 unitsPulse Rate Accuracy: ±3 units ±3 units ±3 unitsMeasurement Wavelengths and Output Powerc:c. This information is especially useful for clinicians performing photodynamic therapy. Red: 660 nanometers @ 0.8 mW max. avg.Infrared: 910 nanometers @ 1.2 mW max. avg.

43Technical InformationSystem SpecificationsTemperature:Operating: -5 °C to 40 °C (23 °F to 104 °F)Storage/Transportation: -40 °C to 70 °C (-40 °F to 158 °F)Humidity:Operating: 10 % to 95 % noncondensingStorage/Transportation: 10 % to 95 % noncondensingOperating Altitude: Up to 12,192 meters (40,000 feet)Operating Hyperbaric Pressure: Up to 4 atmospheresPower Requirements: Two AAA (1.5V) alkaline batteriesBattery Life:Storage: Approx. 9 monthsOperating without Bluetooth: Approx. 48 hours (minimum) of continuous operation Operating with Bluetooth radio – Class 1a:a. When operating with Bluetooth, typical battery life may vary depending on proximity to host connection and configuration of host-to-device communications. Times provided are minimum times for common configurations.Approx. 8 hours minimum Operating with Bluetooth radio – Class 2: Approx. 24 hours minimumDimensions (without sensor or strap): 51 mm x 73 mm x 19 mm (H x W x D)(2.0 in. x 2.9 in. x 0.75 in.)Weight (with batteries and wrist strap): 64.0 g (2.3 oz) Memory: Type: Non-volatile Capacity: up to 1,080 hours (4 sec. data storage rate)up to 540 hours (2 sec. data storage rate)up to 270 hours (1 sec. data storage rate)Classification per IEC 60601-1 / CAN/CSA-C22.2 No. 601.1 / UL60601-1:Type of Protection: Internally powered (battery power)Degree of Protection: Type BF-Applied PartMode of Operation: ContinuousEnclosure Degree of Ingress Protection: IP33

44Technical InformationTransmitterBluetooth Compliance: Version 2.0Operating Frequency: 2.4 to 2.4835 GHzOutput Power: < 20 dBmOperating Range: 100-meter (328-foot) radius indoorsNetwork Topology: Point-to-PointOperation: SlaveAntenna Type: InternalModulation Type: Frequency Shift KeyingFrequency Hopping Spread SpectrumBand Width: 1 MHz

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