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FCC Compliance

 

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 undesignated operation.

 

Federal Communications Commission (FCC) Notice

 

This equipment 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 equipment 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 

equipment off and on. The user is encouraged to try to correct the interference by 

one or more of the following measures:

 

(1) Reorient or relocate the receiving antenna.

 

(2) Increase the separation between the equipment and receiver.

 

(3) Connect the equipment into an outlet on a circuit different from that to which the 

receiver is connected.

 

(4) Consult the dealer or an experienced radio/TV technician for help.

 

The device is designed and manufactured not to exceed the emission limits for 

exposure to radio frequency (RF) energy set by the Federal Communications 

Commission of the U.S. Government. 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 equipment has been shown to be capable of

 

compliance for localized specific absorption rate (SAR) for uncontrolled environment/ 

general population exposure limits specified in ANSI/IEEE Std. C95.1-1992 and has 

been tested in accordance with the measurement procedures specified in IEEE Std. 

1528-200X (Draft 6.5, January 2002).

 

FCC Radiation Exposure Statement

 

For body worn operation, to maintain compliance with FCC RF exposure guidelines, 

use only accessories that contain nonmetallic components. RF exposure separation 

distance is 5 mm. Use of other accessories may violate FCC RF exposure guidelines 

Summary of Contents for Guardian Angel Rx

Page 1: ...Instructions For Use ____________________________________________________________ 7MN00057 00 Guardian Angel Rx Infant Oximeter Module...

Page 2: ...in this manual shall imply Taiwan Aulisa Medical Devices Technologies Inc Aulisa is a registered trademark of Taiwan Aulisa Medical Devices Technologies Inc Taiwan Aulisa Medical Devices Technologies...

Page 3: ...le of Operation 9 Device Set Up 9 Device Pairing 12 Automatic Pairing 12 Manual Pairing 12 Device Power Off 13 Device Charging 13 Alarms 14 Care and Maintenance 14 Cleaning 14 Reuse Life 14 Troublesho...

Page 4: ...3 Guide to Symbols...

Page 5: ...4 MR Unsafe must not be used in an MRI environment...

Page 6: ...2 A functional tester cannot be used to assess the accuracy of this device This device does not require calibration 3 This device readings may be affected by the use of an electrosurgical unit 4 Anem...

Page 7: ...instructions 18 Failure to follow instructions and warnings may result in serious injury or death Cautions 1 This device complies with International Standard IEC 60601 1 2 2014 for electromagnetic com...

Page 8: ...t use caustic or abrasive cleaning agents on the device 12 Do not gas sterilize or autoclave this device 13 Batteries might leak or explode if used or disposed of improperly 14 Follow local governing...

Page 9: ...8 Device Overview Device Components Infant Oximeter Box Infant Oximeter Disposable Sensor Cable Infant Oximeter Reusable Sensor Cable Adhesive Patch Leg Band Charging Adaptor...

Page 10: ...le is reusable Discard the Adhesive Patch after each use Device Intended Use The Aulisa Infant Oximeter Module is intended to measure SpO2 and pulse rate of infant patients during non motion and under...

Page 11: ...with Infant Oximeter Disposable Sensor Cable peel off the release paper on the sensor first and wrap the adhesive patch around the toe If you go with Infant Oximeter Reusable Sensor Cable peel off th...

Page 12: ...he MAIN screen NOTE The power LED will light green when the power is ON NOTE Refer to the Instructions for Use of Guardian Angel Rx Digital Vital Sign Monitoring System for set up instructions and ver...

Page 13: ...er Box Step 4 Press CONFIRM if the serial number SN displayed matches with the one on the Infant Oximeter Box Step 5 To confirm that the process was successful ensure that the Bluetooth connection sta...

Page 14: ...power outlet NOTE The device remains paired with the system until the serial number is deleted from the list NOTE The device must be placed within 32 8 feet 10 meters to Guardian Angel Rx Digital Vit...

Page 15: ...imes of cleaning within 1 5 years of re use life Do not use the device that has exceeded its re use life We recommend you clean and disinfect the device with the instructions below First lightly wipe...

Page 16: ...egrade and do harm to the user CAUTION Do not pour or spray any liquids onto this device and do not allow any liquids to enter any openings in the device CAUTION Do not immerse the device in liquid an...

Page 17: ...to rest comfortably without squeezing or pressing the sensor probe on a hard surface 7 Make sure the device is within 32 8 feet 10 meters spherical radius to the Guardian Angel Rx Digital Vital Sign M...

Page 18: ...le and keep it motionless for at least 10 seconds 2 Relocate the sensor cable to a different site Cannot establish system connection 1 Make sure the device is within 32 8 feet 10 meters spherical radi...

Page 19: ...hown are calculated per Bland JM Altman D 2007 Agreement between methods of measurement with multiple observations per individual Journal of Biopharmaceutical Statistics 17 571 582 Root mean square er...

Page 20: ...ls with combinations of Pulse Amplitude settings of 0 5 1 3 5 7 10 12 15 17 and 20 and SpO2 settings of 100 95 90 85 80 75 and 70 All 1960 combinations of testing points 7 x 28 x 10 of Pulse Rate pass...

Page 21: ...ent Emissions test Compliance Electromagnetic environment guidance RF emissions CISPR 11 Group 1 This device uses RF energy only for its internal function Therefore its RF emissions are very low and a...

Page 22: ...4 4 2 kV for power supply lines 2 kV for power supply lines Mains power quality should be that of a typical commercial or hospital environment Surge IEC 61000 4 5 1 kV Line to Line 1 kV Line to Line...

Page 23: ...22 Magnetic Field IEC 61000 4 8 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...

Page 24: ...the transmitter Field strengths from fixed RF transmitters as determined by an electromagnetic site survey a should be less than the compliance level in each frequency range b Interference may occur...

Page 25: ...iance 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 thedevice b Over t...

Page 26: ...nna 2 Increase the separation between the equipment and receiver 3 Connect the equipment into an outlet on a circuit different from that to which the receiver is connected 4 Consult the dealer or an e...

Page 27: ...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 CAUTION No modifications to this d...

Page 28: ...n the Warranty Period ii purchaser has returned the product to Aulisa in accordance with instructions provided on Aulisa s support webpage and iii Aulisa has verified that the product is defective Aul...

Page 29: ...ttery Life 6 hours of continuous operation Temperature Operating 5 C to 40 C Storage Transportation 25 C to 70 C Humidity Operating 15 to 90 R H non condensing Storage Transportation 10 to 93 R H non...

Page 30: ...29 Internally powered on battery power Type of Protection Type BF Applied Part Mode of Operation Continuous...

Page 31: ...GA AD0001 Infant Oximeter Module Box Disposable Sensor Cable GA OM0011 Infant Oximeter Module Box Reusable Sensor Cable GA OM0009 You may also contact your distributor or contact Aulisa by going onlin...

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