Introduction ............1 Important Safeguards ........2 Warranty ............5 Classifications and Markings ......6 Aeroneb Go System Parts ......7 ® Unit Assembly and Usage ........ 7 Prior to Assembly..........7 Assembly/Functional Test ......... 8 How to Operate the Aeroneb Go Nebulizer ..
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The Aeroneb Go, for use by paediatric and adult patients, ® is intended to aerosolize physician-prescribed solutions for inhalation that are approved for use with a general-purpose nebulizer.
You may finish your treatment and then change (or replace and recharge) the three “AA” batteries immediately. • Do not share your Aeroneb Go Nebulizer with others. ® It is intended for use by a single user. If more than one person uses it, there is a risk of spreading infectious illness.
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The user should ensure that exhaled medication is directed away from bystanders. • Do not microwave any parts. • By connecting the AC/DC adapter to the Aeroneb ® Control Module, the Aeroneb Go Control Module and ® batteries are not being charged.
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Store your Aeroneb Go in the carrying case. ® • Do not store the Aeroneb Go in a location where it is ® exposed to direct sunlight, extreme heat or cold, dust or water. Store out of reach of children. •...
WARRANTY The Aeroneb Go Control Module and AC/DC Adapter are ® warranted for a period of two years from the date of purchase against defects in manufacturing. The Aeroneb Go nebulizer ® unit is warranted for one year from date of purchase against defects in manufacturing.
CLASSIFICATIONS AND MARKINGS The symbols that appear on the Aeroneb Go Nebulizer and ® its accessories are described in the table below: Symbol Meaning Attention, consult accompanying documents Class II equipment per IEC/EN 60601-1 Type BF equipment per IEC/EN 60601-1. This label...
PRIOR TO ASSEMBLY: Check all parts for visible damage. Replace any damaged parts before you use the Aeroneb Go. In the case of missing ® parts, malfunction or damage, contact your local Aeroneb ® representative or equipment supplier.
Insert the nebulizer cable into the back of the nebulizer unit. Add Aeroneb Go base to the bottom of ® the handset. Fill Medication with prescribed nebulizer medication. Never pour more than 6 mL into the cup.
HOW TO OPERATE THE AERONEB GO NEBULIZER ® Turn the Aeroneb Go Control Module ® upside down. Slide the battery cover in the direction of the arrow to remove the lid. Put in three (3) “AA” batteries (not included). Replace the cover on...
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Alternatively, you can power the device by using the AC/DC Adapter if provided (refer page 7). Plug the AC/DC adapter into a standard AC electrical outlet, a green light on the adapter indicates that the AC/DC adapter is turned on. Plug the AC/DC cable into the Control Module, indicated by the DC Voltage Symbol (...
CLEANING AND STORING YOUR AERONEB ® AFTER EVERY USE: Disconnect the control module before you take the nebulizer apart to rinse it. 1. Rinse the Nebulizer Unit (Medication Cup, Nebulizer Body, Base and Mouthpiece or Mask Adapter) under running hot tap water after every use.
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OPTIONAL DISINFECTION: If you would like to disinfect your Aeroneb Go Nebulizer, ® you may choose one of the following two options; Boiling or Vinegar Solution. BOILING: Rinse the Nebulizer Unit (Medication Cup, Nebulizer Body, Base and Mouthpiece or Mask Adapter) under running hot tap water after every use.
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OPTIONAL DISINFECTION VINEGAR SOLUTION: Rinse the Nebulizer Unit (Medication Cup, Nebulizer Body, Base and Mouthpiece or Mask Adapter) under running hot tap water after every use. Shake off excess water, and allow parts to fully air dry on a clean, dry towel, out of the reach of children.
TROUBLESHOOTING GUIDE If you have difficulty operating your Aeroneb Go, check the ® following points: Problem Check Remedy No visible Check that the Using the markings aerosol batteries are under each battery when using inserted correctly. location, place batteries each battery in the Control Module housing.
Check that the Clean the functioning nebulizer has been Aeroneb Go. Refer ® properly cleaned. to page 11. If above remedies do not work, call your local supplier. ELECTROMAGNETIC SUSCEPTIBILITY This device meets the requirements of IEC/EN60601-1-2...
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• Only use the Aeroneb Go nebulizer with components ® specified in the Instructions for Use. Use of the Aeroneb ® Go nebulizer with components other than those specified in the Instructions for Use may result in increased emissions or decreased immunity of the Aeroneb ®...
SPECIFICATIONS Physical Aeroneb Go nebulizer unit (assembled): 40 x 105 x 95 mm Aeroneb Go Control Module: 70 x 110 x 32 mm AC/DC adapter: 74 (H) x 72 (D) x 49 (L) mm Aeroneb Go Nebulizer Unit: 65 g...
PERFORMANCE: Aerosol flow rate: > 0.3 mL/min Average tested flow rate: 0.4 mL/min Particle Size: As measured with the Andersen Cascade Impactor: Specification Range: 1-5 μm. Average Tested: 3.1 μm. As measured with the Marple 298 Cascade Impactor: Specification Range: 1.5-6.2 μm. Average Tested: 3.9 μm.
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50.0 Aerodynamic Size (µm) Power Power Source: Aeroneb Go Control Module - 4.5 VDC (3 “AA” disposable or rechargeable batteries), 350 mA. AC/DC Adapter: 100-240 VAC, 5 VDC, 315 mA, 50-60 Hz. Power Consumption: Less than 2 watts (nebulizing) Patient Isolation: Control module circuitry provides 4 kilovolt...
* Contact your local supplier for reorder number specific for your geographical region. To order replacement parts or accessories, contact your local supplier. If you have any questions or problems regarding your Aeroneb Go nebulizer unit, call your local supplier. ®...
The following Tables are provided in accordance with IEC/ EN 60601-1-2: Guidance and manufacturer’s declaration – electromagnetic emissions The Aeroneb Go nebulizer system is intended for use in the electromagnetic environment specified below. The customer or the user of the Aeroneb Go nebulizer system should assure that it is used in such an environment.
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Recommended separation distances between portable and mobile RF communication equipment and the Aeroneb Go The Aeroneb Go nebulizer system is intended for use in the electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the Aeroneb Go can help prevent electromagnetic interference...
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Guidance and manufacturer’s declaration – electromagnetic immunity The Aeroneb Go nebulizer system is intended for use in the electromagnetic environment specified below. The customer or the user of the Aeroneb Go should assure that it is used in such an environment.
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Note: Ut is the a.c. mains voltage prior to application of the test level. Guidance and manufacturer’s declaration – electromagnetic immunity The Aeroneb Go nebulizer system is intended for use in the electromagnetic environment specified below. The customer or the user of the Aeroneb Go should assure that it is used in such an environment.
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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 Aeroneb Go is used exceeds the applicable RF compliance level above, the Aeroneb Go should be observed to verify normal operation.
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