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Part No. 715-0088, Rev. B
- 11 -
Do not use the AeroNOx 2.0 with helium/oxygen mixtures. The AeroNOx 2.0 is only intended to
deliver NO in conjunction with oxygen/air mixtures.
Anytime a new NO gas cylinder and regulator is used, the user must purge to prevent inadvertent
delivery of NO
2
to the patient.
If the AeroNOx 2.0 is not going to be used within 10 minutes, depressurize the regulator supply line.
If the AeroNOx 2.0 is pressurized and not used within 10 minutes, repeat the purge procedure.
If the AeroNOx 2.0 is not depressurized and not used within 12 hours, repeat the pre-use procedure.
A backup NO delivery system must always be available in the event the primary system should fail.
Set AeroNOx 2.0 alarm thresholds for the current patient conditions to monitor any inadvertent
changes in treatment. For alarm information, see the ALARMS section in the Operators Manual (p/n
715-0086).
Be certain all lines and cables are organized to prevent damage or occlusion.
Use only parts, accessories, transducers, and cables designated by International Biomedical for use
with the AeroNOx 2.0 . Cables and accessories other than those supplied by International
Biomedical may result in unacceptable operation of the AeroNOx 2.0 and will void the equipment
warranty.
The AeroNOx 2.0 samples gas at a rate of 220 mL/min; this can affect the sensitivity of flow triggered
synchronized breath of some ventilators. The trigger sensitivity, if equipped, should be checked after
connecting AeroNOx 2.0 to the breathing circuit.
Do not change NO, NO
2
, or O
2
sensors while in use.
Do not attempt to maintain, diagnose, or repair the AeroNOx 2.0 while delivering NO to a patient.
No modification of the AeroNOx 2.0 is allowed.
Improper sensor or battery replacement will result in a non-functional or inaccurate device.
Sample/Delivery accessories are single patient use only. DO NOT re-use.
Improper maintenance or replacement of sensors may pose a safety risk to the patient. Maintenance
should be performed by qualified service personnel per the instructions.
Perform cylinder connection and purge procedures in well-ventilated areas to prevent inadvertent
exposure to Nitric Oxide or nitrogen dioxide gas. Follow your facilitys safety procedures for handling
medical gas cylinders.
Overexposure to NO or NO
2
can lead to physiological effects such as hypoxia which are not apparent
to the operator.
The IP33 rating applies when the AeroNOx 2.0 is on battery power with the DC Input jack properly
sealed.
Summary of Contents for AeroNO 2.0
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Page 78: ...Par rt No 715 008 88 Rev B 5 12 3 Re 5 12 4 Fr ear Interna ront Intern al Layout al Layout 75 ...
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Page 95: ...Par rt No 715 008 7 3 88 Rev B Nitric Oxid de Sensor S Specificatio 92 ns ...
Page 96: ...Par rt No 715 008 88 Rev B 93 ...
Page 97: ...Par rt No 715 008 7 4 88 Rev B NO2 Senso or Specifica ations 94 ...
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Page 99: ...Par rt No 715 008 7 5 88 Rev B Oxygen Se ensor Spec cifications 96 ...
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