Instruction Manual
6CLASSIFICATIONS AND MARKINGSThe symbols that appear on the Aeroneb® Go Nebulizer and its accessories are described in the table below:Symbol MeaningA
7AERONEB® GO SYSTEM PARTS:Medication Cup CapMouthpieceNebulizer bodyCableBaseControl Module AC/DC Adapter** Available with complete Aeroneb® Go System
8ASSEMBLY/FUNCTIONAL TEST1. Connect the Medication Cup to the Nebulizer Body by lining up the notches on the medication cup and nebulizer body.NOTE:
9HOW TO OPERATE THE AERONEB® GO NEBULIZER3 x AA LR61. Turn the Aeroneb® Go Control Module upside down. Slide the battery cover in the direction of th
10 5. 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 electr
11CLEANING AND STORING YOUR AERONEB® GOAFTER EVERY USE:Disconnect the control module before you take the nebulizer apart to rinse it.1. Rinse the Neb
12OPTIONAL DISINFECTION:If you would like to disinfect your Aeroneb® Go Nebulizer, you may choose one of the following two options; Boiling or Vinegar
13OPTIONAL DISINFECTION2. VINEGAR SOLUTION:i. Rinse the Nebulizer Unit (Medication Cup, Nebulizer Body, Base and Mouthpiece or Mask Adapter) under r
14TROUBLESHOOTING GUIDEIf you have difculty operating your Aeroneb® Go, check the following points:Problem Check RemedyNo visible aerosol when using
15Problem Check RemedyCheck that the AC/DC Adapter is not faulty.Try to operate the Control Module by using batteries instead of the AC/DC Adapter. If
16WARNINGS:• Only use the Aeroneb® Go nebulizer with components specied in the Instructions for Use. Use of the Aeroneb® Go nebulizer with component
17SPECIFICATIONSPhysicalAeroneb Go nebulizer unit (assembled): 40 x 105 x 95 mmAeroneb Go Control Module: 70 x 110 x 32 mmAC/DC adapter: 74 (H) x 72 (
18PERFORMANCE:Aerosol ow rate: > 0.3 mL/minAverage tested ow rate: 0.4 mL/minParticle Size:As measured with the Andersen Cascade Impactor:- Spec
19Representative particle size distribution graph for Albuterol as per EN13544-1 is shown below:Aerodynamic Size (µm)0.1 1 10 100100.050.00.0Cumulat
20REPLACEMENT PARTS AND ACCESSORIES:PART REORDER NUMBERAeroneb® Go System AG-AG4200-XX*Medication Cup Cap AG-AG3010Aeroneb® Go Handset AG-AG4300Mouthp
21Appendix 1EMC tables: The following Tables are provided in accordance with IEC/ EN 60601-1-2:Guidance and manufacturer’s declaration – electromagnet
Recommended separation distances between portable and mobile RF communication equipment and the Aeroneb GoThe Aeroneb Go nebulizer system is intended
Guidance and manufacturer’s declaration – electromagnetic immunityThe Aeroneb Go nebulizer system is intended for use in the electromagnetic environme
Immunity test IEC/EN 60601 Test levelCompliance level Electromagnetic environment – guidancePower frequency (50/60 Hz)Magnetic eldIEC 61000-4-83 A/m
Guidance and manufacturer’s declaration – electromagnetic immunityThe Aeroneb Go nebulizer system is intended for use in the electromagnetic environme
Table of ContentsIntroduction ... 1Important Safeguards ... 2W
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©2013 Aerogen LimitedAG-AG4120-EN Rev D 2013 Manufacturing no.: 30-553 Rev D Aerogen Limited,Galway Business Park,Dangan,Galway,Ireland.www.aerogen.c
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1INTRODUCTION Be sure to read these instructions fully before use.Thank you for purchasing the Aeroneb® Go Nebulizer. Certain conditions such as asthm
2IMPORTANT SAFEGUARDSWhen you use electrical products, always follow basic safety precautions. As with any electrical device take particular care arou
3• Do not use components or attachments that are not recommended by Aerogen. Refer to the Replacement Parts and Accessories section in this manual (p
4• Do not nebulize alcohol-based drugs in an oxygen-rich/high pressure environment.• In event of loss of mains power, remove the AC/DC cable from th
5WARRANTYThe Aeroneb® Go Control Module and AC/DC Adapter are warranted for a period of two years from the date of purchase against defects in manufac
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