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*For all EQUIPMENT and SYSTEMS

 

Guidance and Manufacturer's Declaration - Electromagnetic 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

 

Electromagnetic 

environment -guidance

 

Electrostatic 

Discharge 

(ESD) 

IEC 61000-4-2 

±8 kV contact 

±15 kV air 

±8 kV contact 

±15 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 / 

Burst 

IEC 61000-4-

±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 

Mains power quality 

should be that of a 

typical commercial or 

hospital environment. 

Voltage dips, 

short 

interruptions, 

and voltage 

variations on 

power supply 

input lines 

IEC 61000-4-

11 

0% UT in 0.5 cycle 

at 0°, 45°, 90°, 

135°, 180°, 225°, 

270°, and 315° 

0% UT in 1 cycle at 

0° 

70% UT in 25/30 

cycles at 0° 

0% UT in 250/300 

cycles at 0° and 

180° 

0% UT in 0.5 cycle 

at 0°, 45°, 90°, 

135°, 180°, 225°, 

270°, and 315° 

0% UT in 1 cycle at 

0° 

70% UT in 25/30 

cycles at 0° 

0% UT in 250/300 

cycles at 0° and 

180° 

Mains power quality 

should be that of a 

typical commercial or 

hospital environment. 

Power 

Frequency 

(50/60 Hz) 

30 A/m 

30 A/m 

Power frequency 

magnetic fields 

should be at levels 

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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