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Agu AGU NS12, Instruction Manual

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Agu AGU NS12 Instruction Manual Download Page 16

14 /24page 

9. EMC Tables

 

NS12

 is intended for use in the electromagnetic environment specified 

below. The customer or the user of 

NS12

 must make sure that it is 

used in such an environment. 

Guidance and manufacturer’s declaration - Electromagnetic 

emissions 

Phenomenon 

Professional healthcare 

facility environment

 a)

 

HOME HEALTHCARE 

ENVIRONMENT

 a)

 

Conducted and 

radiated RF 

EMISSIONS 

a) 

CISPR 11 

Group 1 Class B 

Harmonic 

distortion 

Not applicable 

Voltage 

fluctuations and 

flickering 

Not applicable 

a) The equipment is suitable for use in Home Health Environments and 

Professional Health Care Environments limited to patient rooms and 

Summary of Contents for AGU NS12

Page 1: ...irator Model NS12 EN RoHS REACH MDSS GmbH Schiffgraben 41 30175 Hannover Germany AViTA Corporation 9F No 78 Sec 1 Kwang Fu Rd San Chung Dist New Taipei City 24158 Taiwan China AViTA WUJIANG Importer Distributor ...

Page 2: ...RATING THIS UNIT Contents 1 Introduction 1 2 Important Information Before Use 3 3 Product Features 5 4 Battery Installation 6 5 Instructions For Use 8 6 Cleaning and Disinfecting 10 7 Technical Specifications 12 8 Troubleshooting 13 9 EMC Tables 14 10 Explanation of Symbols 18 ...

Page 3: ...ration tip has a comfortable design to prevent the possibility for injury during operation Replaceable Tip Long Short Tip Available Compact Design This device is compact easy to hold and operate It is also safe and comfortable for baby use Battery Operated strong stable Washable Head Module Design Tips collection cup head part can be taken off from the device and washed Collection cup can also be ...

Page 4: ...pact Hygiene Light Weight Low Noise Easy to use while the baby is sleeping NOTE Under any circumstances the device is ONLY for removing nasal secretion Any further medical action should follow the device of doctors ...

Page 5: ...tion of the manufacturer Do not expose the device to extreme temperature very high humidity level or direct sunlight Avoid extreme stress shock or accidental drop down Please replace all batteries when the power or and the sound of the pump is getting weak while using the device It is recommended to remove the batteries if the device will not be used for a period of time The application of pressur...

Page 6: ...oving the nasal secretion only Do not use this device other than the intended purposes During the use of the device the baby should not hold his breath close his mouth or swallow his saliva to avoid vacuum pressure cause eardrum unbalanced If the baby does not feel well when using the device stop and consult a doctor immediately NOTE This Nasal Aspirator must only be used with AViTA NS series Tip ...

Page 7: ...5 24page 3 Product Features Valve Filter optional ...

Page 8: ...polarity symbols Always use new batteries Replace the battery cover Battery operated Always use NEW batteries never mix old and new batteries Do not use rechargeable batteries rechargeable batteries can vary greatly in quality and strength Use of rechargeable batteries may affect the performance of this device Please properly dispose of the batteries away from small children and heat ...

Page 9: ...ed to remove the batteries if the unit will not be used for an extended period of time Batteries must be disposed of in accordance with local environmental and institutional policies Remove the battery during extended storage ...

Page 10: ...ion pressure and ensure the unit is operating correctly before placing in the nostril Hold the baby or child upright the aspirator should not be used while the patient is reclined Be careful not to place the tip too far into the nostril or press against the inside wall of the nostril Press the POWER button to turn on the aspirator on Allow the suction to clear the mucus Repeat in the other nostril...

Page 11: ...n NOTE This mucus may not immediately be visible in the collection reservoir It is recommended that the silicone tip and aspirator head be removed and rinsed between each use to keep any mucus from drying and clogging the device ...

Page 12: ...rubber seal inside the module head be removed for cleaning and to help ensure the unit is fully dry before use and to prevent the growth of bacteria It is recommended at the that the silicone tip and collection cup be at minimum rinsed well with hot water between uses to prevent mucus from drying and clogging the unit To Clean at the end of the day as needed Wash the collection cup and tip with mi...

Page 13: ...us be sucked into the device The head module with filter can only be washed by water it may be rinsed with hot water but should not be cleaned with any soap or chemical cleaners Allow all pieces to dry completely before reassembly NOTE 1 Protect the nasal aspirator from mechanical shock or heavy impact 2 Store the unit in an area away from sunlight dust and humidity 3 The filter optional under val...

Page 14: ...on Tip Soft Silicone Operating environment 16 35 60 8 95 with relative humidity up to 85 non condensing Storage Transportation environment 25 55 13 131 with relative humidity up to 85 non condensing Power supply 2 x 1 5V AA alkaline batteries Weight approx 146g without battery Dimensions approx 98 5mm x 45 3mm x 143mm L x W x H ...

Page 15: ...eck or replace batteries The gray rubber ring located where the collection cup screws in is missing Make sure there is a gray rubber ring where the collection cup screws in The collection cup is not properly screwed in Make sure the three guides on each side of the collection cup line up with the guides on the suction portion of the aspirator ...

Page 16: ... s declaration Electromagnetic emissions Phenomenon Professional healthcare facility environment a HOME HEALTHCARE ENVIRONMENT a Conducted and radiated RF EMISSIONS a CISPR 11 Group 1 Class B Harmonic distortion Not applicable Voltage fluctuations and flickering Not applicable a The equipment is suitable for use in Home Health Environments and Professional Health Care Environments limited to patie...

Page 17: ... environment unless the ME EQUIPMENT and ME SYSTEM used will be connected to the PUBLIC MAINS NETWORK and the power input is otherwise within the scope of the Basic EMC standard Guidance and manufacturer s declaration Electromagnetic immunity Enclosure port Phenomenon Basic EMC standard or test method Immunity test levels Professional healthcare facility environment HOME HEALTHCARE ENVIRONMENT ELE...

Page 18: ...nications equipment transmitters and the NS12 can be requested from supplier using the contact information provided in this manual However it is advisable to keep the electromechanical aerosol equipment at an adequate distance of at least 0 5 m from mobile phones or other RF communications transmitters to minimise possible interference RATED power frequency magnetic fields IEC 61000 4 8 30 A m c 5...

Page 19: ...tient rooms and respiratory treatment facilities in hospital or clinics The more restrictive IMMUNITY acceptance limits have been considered and applied b Before modulation is applied c This test level assumes a minimum distance of at least 15 cm between the ME EQUIPMENT or ME SYSTEM and sources of power frequency magnetic fields ...

Page 20: ...8 24page 10 Explanation of Symbols The CE marking with the Registration Number of the Notified Body This denotes the compliance of European Medical Device Directive 93 42 EEC Medical Device Manufacturer ...

Page 21: ...19 24page Authorized representative in the European Community Date of manufacture YYYY MM DD or YYYY MM Batch code YYMMWWWW Serial number YYMWWWXXXXX ...

Page 22: ...20 24page Keep dry Temperature limit Humidity limitation Atmospheric pressure limitation ...

Page 23: ...sal information Should you wish to dispose of the article do so in accordance with current regulations Details are available from your local authority WEEE 2012 19 EU Directives RoHS This product fulfilling the requirements of the RoHS Directive 2011 65 EU ...

Page 24: ...tive EC 1907 2006 and its amendments do not contain Substances of Very High Concern in concentration above the limit of 0 1 No substance s is are present in the parts of the product above the concentration of 0 1 weight by weight ON OFF push push Device classification type BF ...

Page 25: ...ion against solid foreign objects of 12 5mm and greater and against vertically falling water drops when enclosure tiled up to 15 The empty completely flat batteries must be disposed of through specially designated collection boxes recycling points or electronics retailers You are legally required to dispose of the batteries Importer ...

Page 26: ...24 24page Distributor Model Number Country of Manufacturer Unique Device Identifier NS12P 22240AV 2022 04 22 ...

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