TM Guardian Angel ™ Rx GA2000 Digital Vital Sign Monitoring System Instructions For Use
Read this entire manual carefully before using Aulisa GA2000 Digital Vital Sign Monitoring System. Caution! At the time of publication, this manual is believed to be accurate and up-to-date. In the interest of continued product development, Taiwan Aulisa Medical Devices Technologies, Inc. reserves the right to make changes and improvements to this manual and the products described within at any time, without notice or obligation.
Table of Contents .............................................................................. .......................................................................... Precautions for Use ...... ............................................................................ Intended Use Principle of Operation .................................................................... .......................................................................... System Overview ........................................
Guide to Symbols Refer to instruction manual Type BF-Applied Part (patient isolation from electrical shock) Indicates separate collection for electrical and electronic equipment (WEEE). Non-ionizing electromagnetic radiation. Equipment includes RF transmitters. Interference may occur in the vicinity of equipment marked with this symbol.
Prescription use only Temperature limit NON STERILE IP22 Non-sterile Classification for water ingress and particulate matter Date of Manufacturer Warning Charging Port 2
Precautions for Use Contraindications Caution! 1. Do not use any part of this system in an MRI environment. 2. Explosion Hazard: Do not use this system in an explosive atmosphere or in the presence of flammable anesthetics or gases. 3. This device is not a replacement for a caregiver. Warnings Warning! 3 1. Aulisa GA2000 Digital Vital Sign Monitoring System is intended only as an adjunct in patient assessment. It must be used in with other methods of assessing clinical signs and symptoms. 2.
strangulation or injury to the patient. 7. Be careful with small parts that can be removed from the device and swallowed, such as port covers. They are hazardous to children. 8. Excessive pressure to the sensor application site for prolonged periods may cause damage to the skin beneath the sensor. 9. Do not use a damaged sensor. If the sensor is damaged in any way, discontinue use immediately and replace the sensor. 10.Do not use in or around water or any other liquid when AC power adaptor is used. 11.
Cautions Caution! 5 1. This equipment complies with International Standard IEC 60601-1-2: 2014 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.
components in any liquids. 12.Do not use caustic or abrasive cleaning agents on the device. 13.Do not gas sterilize or autoclave this pulse oximetry system. 14.Batteries might leak or explode if used or disposed of improperly. 15.Follow local governing ordinances and recycling instructions regarding disposal or recycling of the device and device components, including batteries. 16.Do not subject the system to extreme hot or cold temperatures, humidity, or direct sunlight. 17.
Using Aulisa GA2000 Digital Vital Sign Monitoring System This chapter describes how to use Aulisa GA2000 Digital Vital Sign Monitoring System (hereinafter referred to as Aulisa GA2000 system). The system includes the following components and accessories*: *The system comes with either two Pediatric or two Adult Oximeter Sensor Cables.
Adult Oximeter Sensor Cable Pediatric Oximeter Sensor Cable Wristband 8
Charging AdaptorOximeter Box Charging AdaptorDisplay Unit Stand-Display Unit 9
Charging AdaptorReceiver/Transponder ClampReceiver/Transponder StickerReceiver/Transponder Velcro StrapReceiver/Transponder 10
Intended Use TM The Guardian Angel Rx GA2000 Digital Vital Sign Monitoring System is indicated for use in measuring and displaying functional oxygen saturation of arterial hemoglobin (SpO 2 ) and pulse rate of adult and pediatric patients. It is indicated for spot-checking and / or continuous monitoring of patients during non-motion and under well-perfused conditions. The intended environment of use is hospital, medical facilities, home care, and subacute environments. This system is a reusable device.
Device Overview Oximeter Box The Oximeter box includes a Bluetooth transmitter and a sensor chip, which is worn by the patient for vital sign monitoring. It features a sensor chip, along with electronics for vital sign measuring and analyzing. The Oximeter Box must be used within 10 meters from the Receiver/Transponder.
Receiver/Transponder The Receiver/Transponder features Bluetooth/Wi-Fi communication interfaces and an audio/video camera. It receives vital signs monitoring data from the Oximeter Box via Bluetooth, integrates audio and video of the patient, and then converts the data to Wi-Fi signals, which are transmitted to and displayed by the Display Unit.
Display Unit The Display Unit features a 10.1” LCD multi-touch display with Wi-Fi connectivity capability. The Display Unit displays real-time vital signs measured by the Oximeter Box. The Display Unit will display informational text messages, alarm text messages, and beep made audible upon an alarm condition trigger event. The Display Unit incorporates a talking and listening function that allows audio messages to be received and sent via the Receiver/ Transponder.
Displays, Indicators, and Controls This section describes the displays, indicators, and controls for the Aulisa GA2000 System. Display Icons and Indicators Name SpO 2 % bpm Blood Oxygen This icon identifies the window showing the functional blood oxygen saturation in percent. Pulse Rate This icon identifies the window showing the pulse rate in bpm. Pulse Amplitude This icon identifies the window showing the pulse amplitude.
Indicator RT Name Description Measurement Site Status This icon displays whether there is a finger inserted in the sensor. A system alarm will be displayed on the Display Unit if no fingers are detected. Sensor Cable Connection Status This icon displays whether the sensor cable is connected to the Oximeter Box. A system alarm will be displayed on the Display Unit if the cable is disconnected. Battery Level of Oximeter Box These icons signify the battery level at Full, Medium, or Low.
Indicator 17 Name Description Wi-Fi Strength Indicator This icon indicates whether there is a strong connection between the Display Unit and customer Wi-Fi Network. Alarm Indicator This icon identifies an alarm condition exists. !!! represents high priority and !! represents medium priority Alarm Off This icon indicates that the alarm is turned off for the corresponding physiological condition. Audio Paused This icon indicates that the alarm audio is silenced for 2 minutes.
Software Control Buttons Button ALARM LIMITS Name Set Alarm Limits Description Tap on this button on the MAIN screen to adjust the alarm limits for each vital sign. (See “Alarm and Limits” section on page 38 for more information on adjusting the alarm limits.) NOTE: The button is operable only when the system connection is established. System Settings Tap on this button on the top right corner of the MAIN screen to access the settings menu of the system.
Button CONNECTION PAIRING DEFAULT ALARM Name Description Connection Setup In the settings menu, tap on this button to change the Wi-Fi network of the Display Unit or of the Receiver/Transponder, and to modify the password for the Receiver/Transponder. Pair new Oximeter Box or Receiver/ Transponder Restore Default Alarm In the settings menu, tap on this button to restore alarm limits to manufacturer-configured values.
Button Name Pause Alarm Audio Turn Off Alarm Audio Description This button appears on the MAIN screen when an alarm is triggered. Tap on the button to temporarily silence the alarm audio of the current triggered alarm event for 2 minutes. The button appears on the MAIN screen when an alarm is triggered. Tap on the button to permanently silence the alarm audio of the current triggered alarm event.
Use the following procedure to set up the Aulisa GA2000 System: It is recommended to charge the Oximeter Box fully prior to setting up Aulisa GA2000 System as it takes around 3 hours to fully charge and cannot be operated while charging (See “Powering and Charging” section on page 44 for more information.) 1. Connect the charging adaptor (black with a micro USB end) to the Receiver/Transponder and a power outlet. (See “Power and Charging” section on page 47 for more information.
Keep the Receiver/Transponder plugged in at all times. Caution! 2. Press and hold the power On/Off button for three (3) seconds to turn on the Receiver/Transponder. NOTE: The power On/Off LED will light green when the power is on. 3. Connect the charging adaptor (black with Type-C end) to the Display Unit and a power outlet. (See “Power and Charging” section on page 46 for more information.) 4. Press and hold the power On/Off button for three (3) seconds to turn on the Display Unit.
Only use sensor cables supplied or manufactured by Taiwan Aulisa Medical Devices Technologies, Inc. Caution! Do not charge the device via this port. Charging through this port will cause permanent damage to the device. Caution! 7. Secure the wristband onto the patient's wrist with the holder facing outwards. Slip the velcro end through the hole and loop around to secure the wristband. Adjust the wristband according to wrist size, leaving proper space of about one or two fingers to allow ventilation.
9. Click the power On/Off button to turn on the Oximeter Box. NOTE: The power On/Off LED will light green when the power is on. 10. The Receiver/Transponder will automatically connect to a paired Oximeter Box under the control of the Display Unit. NOTE: The Oximeter Box must be placed within 10 meters (32.8 feet) from the Receiver/Transponder. NOTE: The Bluetooth connection status on the Display Unit will turn blue once the connection between the Oximeter Box and the system is established.
System Connection Wi-Fi Network Setup First-Time Users Use the following procedures to establish a Wi-Fi connection between the Display Unit and the Receiver/Transponder: 1. Power the Display Unit and the Receiver/Transponder with their respective charging adaptors. (See “Powering and Charging” section on page 44 for more information.) 2. Press and hold the power On/ Off button for three (3) seconds to turn on the Receiver/Transponder. Wait until the Wi-Fi Link LED on the Receiver/ Transponder blinks red.
6. Select the correct time zone. NOTE: On the top right of the MAIN screen of the Display Unit, ensure the Receiver/Transponder connection indicator is lit blue and the Display Unit Wi-Fi connection indicator has a strong signal. Reset Wi-Fi Network For Display Unit Use the following procedures to change the Wi-Fi network of the Display Unit: 1. On the Display Unit, tap on the “SETTINGS” icon. Then, tap on “CONNECTION”. 2. Tap on “DISPLAY UNIT”. 3.
3. Press and hold the power On/ Off button of Receiver/Transponder for ten (10) seconds until “RESET” is heard. Wait until the Receiver/ Transponder plays a melody (around a minute). 4. Select the desired Wi-Fi network from the list of available connections displayed on the MAIN screen. Enter the network security password. Then, press “CONFIRM”. NOTE: Beware of connecting to an unsecured network provides no security and exposes al your network traffic.
Pairing Oximeter Box The system will automatically scan and pair to the Oximeter Box from the same starter kit only when the connection between the Display Unit and the Receiver/Transponder has been established. NOTE: The Oximeter Box must be used within 10 meters (32.8 feet) from the Receiver/Transponder. NOTE: The Bluetooth connection status icon on the Display Unit will turn blue once the Oximeter Box is paired.
Receiver/Transponder Use the following procedure to manually setup pairing of a new Receiver/ Transponder: NOTE: Only one Receiver/Transponder can be stored on the Display Unit at a time. NOTE: The alarm event history on the Display Unit is managed via the Receiver/Transponder, so you won’t be able to see the current alarm event history when the Display Unit is paired to a new Receiver/ Transponder. 1. Turn on the desired Receiver/Transponder by pressing and holding the power On/ Off button for 3 seconds.
Verifying System Operation Use the following procedure to verify that the alarm systems are working properly. 1. Set up Aulisa GA2000 system according to instructions above. (See “Setting up Aulisa GA2000 system” section on page 21 for more information.) 2. Ensure there is a system connection established between the Oximeter Box, Receiver/Transponder and Display Unit. (See “System Connection” section on page 25 for more information.) 3. Detach the sensor cable from Oximeter Box. 4.
4. Verify that customer Wi-Fi network connection is stable. NOTE: On the top right of the MAIN screen, ensure the Receiver/ Transponder connection indicator is lit blue and the Display Unit Wi-Fi connection indicator has a strong signal. 5. Verify that a SpO2 reading is displayed, that a pulse rate value appears, and that a pulse amplitude reading is displayed. 6. Verify the live video is displayed on the MAIN screen.
Audio/ Video Feature Jane Video: View patient's video 2 3 Listening: Tap to turn on and receive patient’s audio Talking: Press and hold to send an audio message to patient NOTE: When patient privacy is desired, follow the instructions below to place the sticker over the camera and microphone of Receiver/Transponder. The sticker completely blocks the image but may not significantly block the sound.
Shutting off the System Use the following procedure to shut down the Display Unit, the Oximeter Box, and the Receiver/Transponder. Display Unit 1. Press and hold the power On/Off button for at least one (1) second. (A display message will appear.) 2. Choose “Power off” on the display message to turn off the Display Unit. NOTE: The Display Unit can also be put into sleep mode by pressing the “SLEEP” button on the MAIN screen. Oximeter Box Click the power On/Off button to turn off the Oximeter Box.
Alarms and Limits This chapter describes alarms and limits for Aulisa GA2000 System. Alarms The Display Unit provides high and medium priority audible and visual alarms. High Priority Alarms High priority alarms are those that require immediate attention to the patient. They include SpO 2 and pulse rate alarms. On the Display Unit, high priority alarms are indicated with rapid blinking vital sign readings in red color and with alarm text message when alarm limits are met or exceeded.
Medium Priority Alarms Medium priority alarms are those that signal potential problems with the equipment or other non-life-threatening situations. On the Display Unit, medium priority alarms are indicated with slow blinking yellow displays and with alarm text message. NOTE: Alarm LED indicator on the Oximeter Box will blink yellow along with displays on the Display Unit. NOTE: The following table describes alarm conditions and visual indicators.
John O X I M E T E R B O X B AT T E R Y L O W 36
John Smith John 2019-06-03 16:24 150 PR bpm 40 PULSE RATE LOW 50 O X I M E T E R B O X B AT T E R Y L O W NOTE: The volume for audio alarms cannot be adjusted. Silencing alarms does not mean the situation has been resolved. Tapping on “AUDIO OFF” button will permanently silence the alarm audio of the current triggering alarm event. A potential hazard exists if different alarm presets are used for the same or similar equipment in any single area.
Follow the instructions below to review or set alarm limits. To restore alarm settings to default values, refer to “Default Alarm Settings.” 1. Ensure the system connection is established. (See “System Connection” section on page 25 more information.) 2. Tap on "SETTINGS" button on the MAIN screen, and then tap on “ALARM LIMITS” button. John NOTE: Alarm limits can be adjusted only when the Oximeter Box has been paired.
John 150 PR bpm 40 PULSE RATE LOW 50 3. To turn alarm limits on or off, tap on “ON/OFF” button. (Turn on the alarm before adjusting the value.) NOTE: SpO2 max limit is turned off by default. NOTE: There is no alarm setting for pulse amplitude.
4. Tap on ʻʻ + ʼʼ or ʻʻ– ʼʼ buttons or drag the ʻʻseekbarʼʼ to adjust the values. NOTE: The minimum alarm limit cannot exceed the max alarm limit, even if the max alarm limit is turned off. For example, if the max SpO 2 limit is turned off but was previously set at 90%, the min SpO 2 limit cannot be set higher than 90%. If you want to set min SpO 2 limit at 90%, turn on the max SpO 2 limit, set it above 90% and turn it off again as you wish.
When turned off, the alarms will no longer be displayed or sound. Follow the instructions above to turn on the alarms. Consult a physician about the appropriate vital signlimits for the user before adjusting an alarm.
Alarm Delay Function In the traditional alarm management system, upper and lower alarm limits are set so alarms are issued at specific SpO 2 levels. When the SpO 2 level fluctuates near an alarm limit, each breach will trigger an alarm. Aulisa GA2000 monitors the gradient, the depth and the duration of SpO 2 reduction as the factors to determine the alarm riggering delay.
Follow the instructions below to restore alarm settings to default values. 1. Ensure there is a system connection established between the Oximeter Box, the Receiver/Transponder and the Display Unit. See “System Connection” section on page 25 more information.) NOTE: Default alarm settings can be restored only when the system connection is established. 2. Tap on “SETTINGS” button located on the top right corner of the MAIN screen. 3. Tap on “DEFAULT ALARM” button. 4.
Powering and Charging Charging the Oximeter Box Charge the Oximeter Box with the charging adaptor (white) by following the steps below. NOTE: The Display Unit will alarm the user when the Oximeter Box is low on battery. Once on low battery, the Oximeter Box will work for up to another 2 hours (working time on low battery depends on user). 1. Plug the mini-USB end of the cable into the charging port on the Oximeter Box marked by .
2. Attach the wall adaptor to a power outlet. NOTE: The power On/Off LED indicator will light blue while charging and turn off when fully charged. NOTE: It takes about 3 hours to fully charge the Oximeter Box. NOTE: Verify operation of the system (See “Verifying System Operation” section on page 30 for more information) and check the battery status on the MAIN screen of the Display Unit. NOTE: The Oximeter Box cannot be used to measure vital signs while it is being charged.
Powering the Display Unit The Display Unit is meant to be used with the charging adaptor (black with a Type-C end) plugged in. If, for some reason, the Display Unit is disconnected from the charging adaptor, proceed with the following steps to charge and power the Display Unit. The Display Unit will alarm the user when the Display Unit itself is low on battery. 1. Plug the Type-C end of the charging adaptor (black with a Type-C end) into the Display Unit. 2. Attach the wall adaptor to a power outlet. 3.
Powering the Receiver/ Transponder The Receiver/Transponder is meant to be used with the charging adaptor (black with micro-USB end) plugged in. 1. Plug the micro-USB cable end of the charging adaptor into Receiver/Transponder. 2. Plug the wall adaptor to a power outlet. NOTE: The AC power LED indicator will light green when AC adaptor is ON. NOTE: The charging LED indicator will light blue when internal battery is charging and will turn off when it is fully charged.
Care and Maintenance The advanced digital circuitry within the Oximeter Box of this system requires no calibration or periodic maintenance, neither does the Display Unit or the Receiver/Transponder. Field service or repair of this system is not possible. Do not attempt to open the case. Opening the Oximeter Box, the Receiver/Transponder or the Display Unit will damage the device and void the warranty. If the system is not functioning properly, see “Troubleshooting” section on page 48 for more information.
Troubleshooting Problem Possible Solution Click the power On/Off button. Cannot turn on the Oximeter Box Cannot turn on the Display Unit Cannot turn on the Receiver/Transponder Unable to obtain a valid SpO 2 or pulse rate reading NOTE: In some instances, patient perfusion may be inadequate for pulse detection. Fully charge the Oximeter Box until the blue LED goes off. Press and hold the power On/Off button for at least three (3) seconds.
Problem Possible Solution Make sure the system connection is established. Reduce or eliminate any interference. Make sure that the finger sensor is not placed on the same wrist being used for other patient therapies or diagnostics (e.g. blood pressure cuff). Unable to obtain a valid SpO 2 or pulse rate reading. NOTE: In some instances, patient perfusion may be inadequate for pulse detection. Make sure the sensor probe is attached to the finger securely.
Problem Possible Solution Make sure the sensor probe is attached to the finger securely. Unstable/Constant SpO 2 and Pulse Rate readings Make sure the sensor cable is securely attached to the Oximeter Box. Check the sensor cable for any visible signs of deterioration. Reduce patient motion. Make sure the sensor cable is securely attached to the Oximeter Box. A dash “---” appears in the vital sign display. Make sure the sensor probe is attached to the finger securely.
Problem The unit is in Alarm mode, but no audible alarms can be heard. Possible Solution Wait for two minutes and alarm tones will automatically re-engage if it was silenced temporarily. Make sure there are no headphones inserted into the headphone jack of the Display Unit. Ensure that the Oximeter Box is within 10 meters spherical radius to Receiver/ Transponder while being paired.
Device Performance SpO 2 Accuracy SpO 2 accuracy testing is performed by in vivo accuracy testing under laboratory conditions on healthy adult subjects with varying skin pigmentation in an independent research laboratory through induced hypoxia studies. Analysis of bias1 was performed vs. Hemoximeter data. The limits of agreement shown are calculated per: Bland JM, Altman D. (2007) Agreement between methods of measurement with multiple observations per individual.
2 2 The graph below shows the error (SpO 2 -SaO 2 ) plots of each subject measured by the Aulisa GA2000 with upper and lower 95% limits of agreement. Each sample data point is from a clinical study in healthy adult volunteers. 2 Pulse Rate Accuracy Pulse rate accuracy has been functionally tested against an electronic pulse simulator at 30, 50, 80, 100, 150, 200, 250, and 290 bpm, with combinations of Pulse Amplitude settings of 0.
Manufacturer's Declaration Refer to the following table for specific information regarding compliance to IEC 60601-1-2 for this device. Guidance and Manufacturer's Declaration - Electromagnetic Emissions - for all EQUIPMENT and SYSTEMS Guidance and Manufacturer's DeclarationElectromagnetic Emission This 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.
Guidance and Manufacturer's Declaration-Electromagnetic Immunity - for all EQUIPMENT and SYSTEMS Guidance and Manufacturer's DeclarationElectromagnetic Immunity This 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.
Immunity test IEC 60601-1-2 test level Compliance level Voltage dips, short interruptions, and voltage variations on power supply input lines Electromagnetic environmentguidance Mains power quality should be that of a typical commercial or hospital environment. IEC 61000-4-11 Power Frequency (50/60 Hz) Magnetic Field 30 A/m IEC 61000-4-8 30 A/m Power frequency magnetic fields should be at levels characteristic of a typical location in a typical commercial or hospital environment.
Guidance and Manufacturer's Declaration-Electromagnetic Immunity-for EQUIPMENT and SYSTEMS that are not LIFE-SUPPORTING Guidance and Manufacturer's DeclarationElectromagnetic Immunity This 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.
NOTE 1 At 80 MHz and 800 MHz, the higher frequency range applies. NOTE 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.
FCC Compliance For Oximeter Box Declaration of Conformity with FCC for Electromagnetic Compatibility This device 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.
The FCC requires the user to be notified that any changes or modifications to this device that are not expressly approved by Taiwan Aulisa Medical Devices Technologies, Inc. may void the user's authority to operate the equipment. For Display Unit & Receiver/Transponder Declaration of Conformity with FCC for Electromagnetic Compatibility This device complies with Part 15 of the FCC Rules.
When suing IEEE 802.11a wireless LAN, this product is restricted to indoor use, due to its operation in the 5.15 to 5.25GHz frequency range. The FCC requires this product to be used indoors for the frequency range of 5.15 to 5.25GHz to reduce the potential for harmful interference to co channel mobile satellite systems. High-power radar is allocated as the primary user of the 5.25 to 5.35GHz and 5.65 to 5.85GHz bands. These radar stations can cause interference with and/or damage to this device.
Service, Support, and Warranty Warranty under “Contact Us”.
Device Privacy Policy This Privacy Policy was last updated on March 22, 2019. Our Policy This privacy policy applies to personal information collected by Taiwan Aulisa Medical Devices Technologies, Inc. (”Aulisa”, “we”, “us” and/or “our”) from users of the Aulisa remote patient monitoring devices (the “Devices”). “Personal Information” includes any information that can be used on its own or with other information to identify or contact a single person or to identify an individual in context.
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(7) protect our rights, privacy, safety or property, and/or that of yours or others; and (8) allow us to pursue available remedies or limit the damages we may sustain. Failure to Provide Information Providing your Personal Information is not statutorily or contractually mandated. If you choose not to provide this information, we cannot monitor your vital signs, and you will be unable to use our Devices.
We consider your information to be a vital part of our relationship with you. There are, however, certain circumstances in which we may share your Personal Information with certain third parties without further notice to you. Those circumstances are described below: With Our Provider Customers: If you are a Patient, we will share your Personal Information and Health Data with our Provider Customer(s) that provide healthcare services to you.
How Long Will You Retain the Information? We only store certain of your Personal Information for as long as you use the Devices and up to five (5) years after you cease to use the Devices. At the end of this five-year period, we will remove your Personal Information from our databases and will request that our business partners remove your Personal Information from their databases.
information@aulisa.com.
Where our processing of your Personal Information is based on consent, you have the right to withdraw that consent without detriment at any time by contacting us at information@aulisa.com . You can also exercise the rights listed above at any time by contacting us at information@aulisa.com . How Can I Update, Correct or Delete My Personal Information? If you need to make changes or corrections to your information, you may make such changes or corrections on the Device.
Specifications Aulisa GA2000 Digital Vital Sign Monitoring System Blood Oxygen Saturation Display Range (SpO 2 ) Pulse Rate Display Range Accuracy Blood Oxygen Saturation (%SpO 2 ) (± 1 S.D.
Measurement Wavelengths and Output Power Red Infrared 660 nanometers @ 1.8 mw nominal 905 nanometers @ 2 mw nominal Bluetooth Communication Range Protocol Direction Data rate 10-meter spherical radius Bluetooth 4.0 Bi-direction Up to 100kBps Wi-Fi Communication Protocol Direction 802.11 b/g/n/ac, 2.
Oximeter Box Internal Power Battery Operating Life Dimensions Without sensors 3.7 V battery 22 hours of continuous operation 0.7” x 1.3” x 2.7” 16 mm x 32 mm x 68 mm Weight 1 oz 28 g Wireless Communication Bluetooth IP22 Ingress Protection Display Unit Display Display panel Power Requirements Mains DC Input 10.1” IPS Touch Panel 100-240 V AC 50-60 Hz 5 V DC/AC adaptor Internal Power Battery Operating Life Dimensions 3.8 V battery 2 hours of continuous operation 7.04” x 10.35” x 0.
Dimensions Body Stand 2.6” x 4.6” x 2.7” 67 mm x 116 mm x 69 mm 3.5” x 3.6” x 1.
Parts and Accessories Model Number Oximeter Box GA-SM0001 Adult Oximeter Sensor Cable GA-RS0002 Pediatric Oximeter Sensor Cable GA-RS0004 Wristband GA-WB0002 Receiver/Transponder GA-RT0001 Display Unit GA-DU0003 Stand- Display Unit GA-SD0002 Charging Adaptor-Oximeter Box GA-CS0001 Charging Adaptor-Display Unit GA-CD0004 Charging Adaptor-Receiver/Transponder GA-CR0001 For more information about Aulisa parts and accessories, contact your distributor, or contact Aulisa by going online at ww
