microlife NEB NANO basic Portable Compressor Nebuliser Instruction Manual

microlife NEB NANO basic Portable Compressor Nebuliser

Portable Compressor Nebuliser

1. Piston compressor
2. ON/OFF button
3. Power indicator
4. USB Port
5. Air filter compartment
6. Air outlet
7. Nebuliser
   -a: Vaporiser head
8. Air tube
9. Mouthpiece
   AT Nose piece
   AK Adult face mask
   AL Child face mask
   AM Air filter
   AN Micro USB cable
   AO AC adapter
   AP Assembling nebuliser kit
   AQ Replacing air filter

Dear Customer,
This nebuliser is an aerosol therapy system suitable for domestic use. This device is used for the nebulisation of liquids and liquid medication (aerosols) and for the treat-ment of the upper and lower respiratory tract.
If you have any questions, problems or want to order spare parts please contact your local Microlife-Customer Service. Your dealer or pharmacy will be able to give you the address of the Microlife dealer in your country. Alter- natively, visit the internet at www.microlife.ru where you will find a wealth of invaluable information on our prod-ucts.
Stay healthy – Microlife AG!

Explanation of Symbols

• Batteries and electronic devices must be disposed of in accordance with the locally applicable regulations, not with domestic waste.
• Read the instructions carefully before using this device.
• Type BF applied part
• Class II equipment
• Serial number
• Reference number
• Manufacturer
• ON
• OFF
• Protection against solid foreign objects and harmful effects due to the ingress of water
• Conformity mark
• A single mark of product circulation on the market of the Eurasian Economic Union member state
• CE Marking of Conformity

Important Safety Instructions

• Follow instructions for use. This document provides important product operation and safety information regarding this device. Please read this document thor-oughly before using the device and keep for future reference.
• This device may only be used for the purposes described in these instructions. The manufacturer cannot be held liable for damage caused by incorrect application.
• Retain instructions in a safe place for future reference.
• Do not operate the unit in presence of any anesthetic mixture inflammable with oxygen or nitrogen protoxide.
• This device is not suitable for anaesthesia and lung ventilation.
• This device should only be used with original acces-sories as shown in these instructions.
• Do not use this device if you think it is damaged or notice anything unusual.
• Never open this device.
• This device comprises sensitive components and must be treated with caution. Observe the storage and operating conditions described in the «Technical Specifications» section.
• Protect it from:
  • water and moisture
  • extreme temperatures
  • impact and dropping
  • contamination and dust
  • direct sunlight
  • heat and cold
• Comply with the safety regulations concerning the electrical devices and in particular:
  • Never touch the device with wet or moist hands.
  • Place the device on a stable and horizontal surface during its operation.
  • Do not pull the power cord or the device itself to unplug it from the power socket.
  • The power plug is a separate element from the grid power; keep the plug accessible when the device is in use.
• Before plugging in the device, make sure that the electrical rating, shown on the rating plate on the bottom of the unit, corresponds to the mains rating.
• In case the power plug provided with the device does not fit your wall socket, contact qualified personnel for a replacement plug with that of a suitable one. In general, the use of adapters, simple or multiple, and/or extension cables is not recommended. If their use is indispensable, it is necessary to use types complying with safety regulations, paying attention that they do not exceed the maximum power limits, indicated on adapters and extension cables.
• Do not leave the unit plugged in when not in use; unplug the device from the wall socket when it is not in operation.
• The installation must be carried out according to the instructions of the manufacturer. An improper installa-tion can cause damage to persons, animals or objects, for which the manufacturer cannot be held responsible.
• Do not replace the USB cable nor the AC adapter of this device. In case of damage, have them replaced by a service centre authorised by the manufacturer.
• The power supply cord should always be fully unwound in order to prevent dangerous overheating.
• Before performing any maintenance or cleaning operation, turn off the device and disconnect the plug from the main supply.
• Only use the medication prescribed for you by your doctor and follow your doctor’s instructions with regard to dosage, duration and frequency of the therapy.
• Depending on the pathology, only use the treatment that is recommended by your doctor.
• Only use the nose piece if expressly indicated by your doctor, paying special attention NEVER to introduce the bifurcations into the nose, but only positioning them as close as possible.
• Check in the medicine instruction leaflet for possible contraindications for use with common aerosol therapy systems.
• Do not position the equipment so that it is difficult to operate the disconnection device.
• For greater hygienic safety, do not use the same accessories for more than one person.
• Never bend the nebuliser over 60°.
• Do not use this device close to strong electromagnetic fields such as mobile telephones or radio installations. Keep a minimum distance of 3.3 m from such devices when using this device.

Ensure that children do not use this device unsu-pervised; some parts are small enough to be swal-lowed. Be aware of the risk of strangulation in case this device is supplied with cables or tubes.
Use of this device is not intended as a substitute for a consultation with your doctor.

Preparation and Usage of this Device

Prior to using the device for the first time, we recommend cleaning it as described in the section «Cleaning and Disinfecting».

1. Assemble the nebuliser kit AP. Ensure that all parts are complete.
2. Fill the nebuliser with the inhalation solution as per your doctor’s instructions. Ensure that you do not exceed the maximum level.
3. Connect one end of the air hose 8 to the dedicated outlet at the bottom of the nebuliser AP and the other end to the air outlet 6 on the device.
4. Start the nebulisation by pressing the ON/OFF button 2; the power indicator 3 will light up orange.
5. Place the mouthpiece 9 in the mouth or fit one of the face masks over mouth and nose.
   • The mouthpiece gives you a better drug delivery to the lungs.
   • Choose between adult AK or child face mask AL and make sure that it encloses the mouth and nose area completely.
   • Use all accessories including the nose piece AT as prescribed by your doctor.
6. During inhalation, sit upright and relaxed at a table and not in an armchair, in order to avoid compressing your respiratory airways and impairing the treatment effectiveness. Do not lie down while inhaling. Stop inhalation if you feel unwell.
7. After completing the inhalation period recommended by your doctor, press the ON/OFF button 2 to turn off the device.
8. Empty the remaining medication from the nebuliser and clean the device as described in the section «Cleaning and Disinfecting».

This device was designed for intermittent use of 30 min. On / 30 min. Off.
Switch off the device after 30 min. use and wait for another 30 min. before you resume treatment.
The device requires no calibration.
No modification to the device is permitted.

Cleaning and Disinfecting

Thoroughly clean all components to remove medication residuals and possible impurities after each treatment. Use a soft and dry cloth with non-abrasive cleaners to clean the compressor.
Make sure that the internal parts of the device are not in contact with liquids and that the power plug is disconnected.

Cleaning and disinfecting of the accessories
Follow carefully the cleaning and disinfecting instructions of the accessories as they are very important to the performance of the device and success of the therapy.

Before and after each treatment
Disassemble the nebuliser 7 by turning the top counter-clockwise and remove the medicine conduction cone. Wash the components of the disassembled nebuliser, the mouthpiece 9 and the nose piece AT by using tap water; dip in boiling water for 5 minutes. Reassemble the nebuliser components and connect it to the air tube connector, switch the device on and let it work for 10-15 minutes.

• Wash masks and air tube with warm water.
• Only use cold disinfecting liquids following

Maintenance, Care, and Service

Order all spare parts from your dealer or pharmacist, or contact Microlife- Service (see foreword).

Replacement of the nebuliser
Replace the nebuliser 7 after a long period of inactivity, in cases where it shows deformities, breakage, or when the vaporiser head 7-a is obstructed by dry medicine, dust, etc. We recommend to replace the nebuliser after a period between 6 months and 1 year depending on the usage.
Only use original nebulisers!

Replacement of the air filter
In normal conditions of use, the air filter AM must be replaced approximately after 100 working hours or after each year. We recommend to periodically check the air filter (10 – 12 treatments) and if the filter shows a grey or brown colour or is wet, replace it. Extract the filter and replace it with a new one.

• Do not try to clean the filter for reusing it.
• The air filter shall not be serviced or maintained without filter!

Malfunctions and Actions to take

The device cannot be switched on

• Make sure that the plugs are properly inserted in the power outlet and the device.

The nebuliser functions poorly or not at all

• Ensure the air tube 8 is correctly connected at both ends.
• Ensure the air tube is not squashed, bent, dirty or blocked. If necessary, replace with a new one.
• Ensure the nebuliser 7 is fully assembled and the colored vaporiser head 7-a is placed correctly and not obstructed.
• Ensure the required medication has been added.
• Ensure the air filter AM is mounted properly (device is  noisy).

Guarantee

This device is covered by a 2 year guarantee from the date of purchase. During this guarantee period, at our discretion, Microlife will repair or replace the defective product free of charge.
Opening or altering the device invalidates the guarantee.
The following items are excluded from the guarantee

• Transport costs and risks of transport.
• Damage caused by incorrect application or non-compliance with the instructions for use.
• Damage caused by leaking batteries.
• Damage caused by accident or misuse.
• Packaging/storage material and instructions for use.
• Regular checks and maintenance (calibration).
• Accessories and wearing parts: Batteries, nebuliser, masks, mouthpiece, nose piece, tube, filters, micro USB cable, AC adapter (optional).

Should guarantee service be required, please contact the dealer from where the product was purchased, or your local Microlife service. You may contact your local Microlife service through our website: www.microlife.com/support
Compensation is limited to the value of the product. The guarantee will be granted if the complete product is returned with the original invoice. Repair or replacement within guarantee does not prolong or renew the guar-antee period. The legal claims and rights of consumers are not limited by this guarantee.

Technical Specifications

• Nebulisation rate: 0.25 ml/min. (NaCI 0.9%)

• Particle size: 65% < 5 µm 2.9 µm (MMAD)

• Operating pressure: 0.25 ~ 0.5 bar

• Acoustic noise level: 45 dBA

• AC adapter: Input: 100-240VAC 50/60Hz 0.5A Output: 5V DC 2A

• Nebuliser capacity: min. 2 ml; max. 6 ml

• Residual volume: 0.8 ml

• Operating limits: 30 min. On / 30 min. Off

• Operating conditions: 10 – 40 °C / 50 – 104 °F
  10 – 95 % relative maximum humidity
  700 – 1060 hPa Atmospheric pressure

• Storage and shipping conditions: -20 – +60° C / -4 – +140 °F 10 – 95 % relative maximum humidity
  700 – 1060 hPa Atmospheric pressure

• Weight: 180 g

• Dimensions : 117 x 69 x 46 mm

• IP Class: IP22

• Reference to standards:
  EN 13544-1; EN 60601-1;
  EN 60601-2; EN 60601-1-6;
  IEC 60601-1-11

• Expected service life: 400 hours

This device complies with the requirements of the Medical Device Directive 93/42/EEC.
Class II device as regards protection against electric shocks.
Nebuliser, mouthpiece and masks are type BF applied parts.

Guarantee Card
Name of Purchaser
Serial Number
Date of Purchase
Specialist Dealer

Globalcare Medical Technology Co., Ltd
7th Building, 39 Middle Industrial Main Road, European Industrial Zone, Xiaolan Town,
528415 Zhongshan City, Guangdong Province, PRC

References

• Hypertension and Fever Management - Microlife AG
• Support - Microlife AG
• Microlife. Partner pro lidi. Pro život. - Microlife AG

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