HOFFEN A500LW09 Compressor Nebulizer Instruction Manual

**HOFFEN A500LW09 Compressor Nebulizer Instruction Manual

**

INTRODUCTION

Thank you for choosing our product. We are certain that you will enjoy it. Please carefully read this instruction manual before using the product, specifically the safe use, cleaning, and storage directions. Please save this instruction manual for future reference.

TECHNICAL SPECIFICATION

• Model: A500LW09
• Batch no.: 039/22 Material: ABS
• Supply voltage: 230 V~, 50/60 Hz
• Power: 180 W
• Noise level: approx. 60 dBA
• Medicine chamber volume: 10 ml
• Average inhalation rate: 0.3 ml/min (2% saline solution)
• Flow range: 5 ~ 8 l/min
• Particle size: 0.5–10 µm MMAD: 3 µm
• C ompressor pressure range: 29–52 Psi (200–360 kPa / 2–3.6 bars)
• Operating pressure range: 11.6–19 Psi / 80–130 kPa / 0.8–1.3 bars
• Operating humidity range: Relative humidity 15–93%
• Operating temperature range: 5°C–40°C
• Storage temperature range: –25°C–70°C
• Storage humidity range: 15–93% RH
• Dimensions: 185 x 120 x 185 mm
• Net weight: 1.44 kg
• Gross weight: 1.68 kg
• Age: 3+ (markers only)

CONTENTS

After unpacking, make sure that none of the listed elements are missing and check the device for proper operating order.

|
---|---
1 x air compressor nebulizer, 1 x child-sized mask, 1 x adult-sized mask, 5 x replacement air filters, 1 x air tube, 3 x markers, 1 x mouthpiece, 1 x medicine chamber| 1 x instruction manual

INTENDED USE

• The device is intended for personal indoor use only and may not be used for commercial purposes. Any other use is considered improper and therefore dangerous.
• The manufacturer is not responsible for any injuries resulting from improper use of the device.
• WARNING! Modification of the product is strictly prohibited.
• The product is intended for inhalation of the upper respiratory system.
• To ensure proper operation of the product, it is necessary to use all the parts described in section 6 – the parts conform to standard EN 13455

Additional information:
The product information complies with European standard EN 13455 and may not be applicable to suspension or high viscosity medication. In such cases, please contact the medicine provider for directions.

SAFETY GUIDELINES

Please carefully read the instruction manual before first use. Always follow the recommendations of the instruction manual when using the device. Please keep the packaging and instruction manual for future reference, as they contain important information.

• The device cannot be used by children. Keep the device out of the reach of children.
• Children are not permitted to play with the device.
• Children cannot clean or perform maintenance on the device without supervision.
• The device can be used by children aged 8 and over and people with mental or sensory restrictions or without the required knowledge and experience as long as they are supervised or instructed in scope of safe use of the device and understand the potential hazards
• Use the appliance according to the instruction manual only.
• Attention: If you do not read or obey all safety measures, you are at risk of physical injury or damage to the device.
• Inhalations with the nebulizer cannot serve as substitute for a doctor’s appointment.
• Not suitable for use in anaesthetic respiratory systems or lung ventilator respiratory systems.
• Keep the device away from water.
• Do not use a damaged device.
• Do not use near open flame.
• Always remember to disconnect the device from the power source during cleaning, filling, and after every use.
• The device is not waterproof. To avoid electric shock, make sure no water or other liquids get inside the device. Do not submerge the power cord or the device in water. Do not use when taking a bath. Do not touch the device if it should fall into water or get soaked. Immediately pull the plug out of the outlet.
• Please regularly check the condition of the device. Never use the device if any of its parts (including the power cord) are damaged or if it has been dropped or submerged in water. In such instances, send it to a service point for inspection and repairs.
• Never use the device in proximity of flammable gases, oxygen, or in sprayed rooms.
• Never leave an unused device connected to a power source.
• Only the power cord included with the nebulizer may be used with the device. Do not use any other cords unless they are recommended by the manufacturer.
• Never attempt unauthorised repairs of the device. All maintenance activity should be left to qualified servicing staff.
• The air compressor nebulizer is not intended to work in proximity of electrosurgical equipment.
• WARNING! Mobile communication devices (including peripheral devices such as antenna cables and outdoor antennas) should be used in proximity no greater than 30 cm from any part of the device, including the cords specified by the manufacturer. Otherwise, the operating order of said equipment may deteriorate.
• The product can be used under adult supervision only.
• Make sure to keep the proper position during the nebulisation process.
• The product can be coloured under adult supervision when it is disconnected from the power source. The product cannot be coloured during the inhalation process or when the device is turned on.

The instruction manual is also available in electronic format at info@joinco.com.pl

PRODUCT DESCRIPTION

The colour markers, which the child can use to colour the bear before the start of inhalation, can be used to colour the device only with preservation of the safety standards. The markers can be easily washed off with a paper towel or cloth. The A500LW09 air compressor nebulizer is a compact device used for respiratory airway inhalation. The device produces a stream of air, which runs thought the transparent tube to the atomiser in order to turn the prescribed medication into a spray mist to make it easier to inhale. The processed medication mist runs through the mouthpiece and can be inhaled by the patient. The device facilitates safe administration of prescribed medication.

Attention: before colouring, please read section 5. SAFETY GUIDELINES

1. Power switch
2. Handle
3. Vents
4. Filter
5. Connector
6. Air tube
7.  Medication chamber
8. Mouthpiece
9. Adult-sized mask
10. Child-sized mask
11. Replacement air flters
12. Markers

SAFE USE DIRECTIONS

Note:
The nebulizer should be thoroughly cleaned before use according to section 8. Cleaning the device

1. Place the compressor nebulizer on a flat and stable surface. Be sure that you can easily reach the control elements when you are seated.

2. Remove the inside accessories. Important: Before first use, the nebulizer should be thoroughly cleaned according to section 8. Cleaning the device.

3. Gently turn the top part of the medicine chamber to the left to open it. Place cone inside and fill with the medication.
   

4. Fill the bottom part of the medicine chamber with the prescription medication. Make sure that the blue cone is inside the bottom part. The two tabs of the yellow spacer should be pointing upwards.

5. Gently turn the top part to the right to reassemble the medicine chamber. Be sure that both parts fit.

6. Attach one end of air tube to the base of the medicine chamber.

7. Attach the other end of air tube to the connector.

8. Attach the mouthpiece or selected mask to the top part of the medicine chamber.

9. Plug the power cord into an appropriate electrical outlet. At this stage, make sure that the power switch is in position “O”.

10. Press power switch to start your prescribed procedure. Important:
    The compressor motor is equipped with a thermal safeguard, which will turn off the device if it should overheat. When the thermal protector turns off the device, please:
    a. Turn the device off;
    b.  Unplug the device from the electrical outlet;
    c.  Wait 30 minutes for the motor to cool down before the next procedure. Make sure the air vents are not clogged.

11. When the procedure is finished, turn off the device and unplug it from the electrical outlet

CLEANING THE DEVICE

It is recommended that the medicine chamber, mouthpiece and mask be thoroughly cleaned with warm water after every use. If your physician or therapist specifies a different cleaning procedure, please follow their instructions.

Rinsing (after each procedure):

1. Disconnect the air tube, medicine chamber, mouthpiece, and mask.
2. Gently turn the medicine chamber to open it.
3. Rinse the medicine chamber, mouthpiece, and mask with warm water.
4. Dry with a clean soft towel and leave to dry.
5. Reassemble the nebulizer when completely dry and put the parts in a dry and tight container.

DISINFECTIONS:
Please follow the steps listed below to disinfect your nebulizer, unless your physician instructs otherwise. The device is recommended to be disinfected after the final procedure of the day.

1. Combine one part vinegar with three parts distilled water. Make sure there is enough of the mixed solution to submerge the medicine chamber, mouthpiece and mask.
2. Perform rinsing steps 1–3.
3. Wash the medicine chamber, mouthpiece and mask in warm water and then with hot running water.
4. Submerge the parts in the vinegar and water solution for 30 minutes.
5. Perform rinsing steps 3–5.

CLEANING THE CASING

1. Wipe with a damp cloth every day.
2. Do not use any powdered cleaning agents or cleaners, which may damage the surface.

FILTER CHANGE

1. Do not use cotton or any other textiles. Do not wash or clean the filter. Use only the recommended filters. Do not use the device without a filter.
2. Change the filter every 30 days or when it turns gray.
3. Changing the filter:
   
   A. Open the filter cover
   B. Replace the used filter with a new one.
   C. Close the filter cover

STORAGE AND TRANSPORT

STORAGE:
If you do not intend to use the device for a long time, we recommend placing the product in the original packaging and store it in closed space. Protect the product from direct sunlight, moisture, dust, and other contaminants.

TRANSPORT:
If you want to transport the product, we recommend placing it in its original packaging. Protect the product from direct sunlight, moisture, dust, other contaminants, and shocks.

REPLACEMENT PARTS

Please contact Joinco Polska sp. z o.o. should you want to purchase any of these elements.

DISPOSAL OF WASTE EQUIPMENT

Waste electrical devices are recyclables – never dispose them into household waste containers because they may contain substances dangerous to human health and the environment! Please help us actively manage natural resources and protect the natural environment by taking the waste device to a recyclable electric waste storage point.

WARRANTY

The product comes with a 3-year warranty. In the event of a malfunction, please return the product to the point of its purchase. Remember to present proof of purchase. The product should be complete and in its original packaging.

DECLARATION OF CONFORMITY WITH EUROPEAN STANDARDS

mouthpiece, air tube, filter, medication chamber

masks, nebulizer markers

SYMBOLS

This symbol means that the product comes with an instruction manual, which should be read before use.

 When the “Green Dot” restriction appears on packaging, it signifies that the importer has made a financial contribution towards development and operation of the national packaging recovery and recycling system in accordance with the standards resulting from the laws of Poland and the European Union on packaging and packaging waste.

 Ingress protection provided by enclosures. 2 – protection against foreign solid bodies with a diameter of 12.5 mm and greater; 1 – protection against raindrops of water.

 BF applied part

This product fulfils the requirements of Directive 2011/65/EU – the so-called RoHS Directive. The Directive aims to lay down the rules for Member State laws concerning restriction of hazardous substances in electrical and electronic equipment and contribute to the protection of human health and the environmetally sound recovery and disposal of waste electrical and electronic equipment. The RoHS Directive is in effect from 3 January 2013. New marketed electric and electronic equipment does not contain lead, mercury, cadmium, chromium VI, polybrominated diphenyl or polybrominated phenyl ether.

Shock protection safety class symbol II.

 Product production date.

 Lot number designation.

 Manufacturer’s data.

 Important information – please read attached documentation

 For indoor use only.

 Designation of the packaging material – corrugated cardboard.

 Authorised representative’s data.

Not appropriate for children aged 36 months and under. Small parts. Choke hazard.

 Packaging elements are to be disposed into appropriate containers.

 Designation of the container to dispose the packaging – paper

DETERMINATION OF ELECTROMAGNETIC COMPATIBILITY

This device requires special safeguards in scope of electromagnetic compatibility (EMC), which must be installed and started in accordance with the information provided on EMC. This device may be affected by portable and mobile radio communication devices.

Note: This device has been thoroughly checked to ensure proper operating order. Caution: Do not use this device near or on other devices. If such use is necessary, observe the device in order to verify the accuracy of operation in the used configuration. Warning: The use of accessories, transducers, and cords other than those provided may result in increased emission or reduced resistance of the product.

Manufacturer’s guidelines and declarations — electromagnetic emissions

The A500LW09 compressor nebuliser is intended for use in the electromagnetic environment described below. The customer or the user of the A500LW09 compressor nebuliser should ensure its use in such an environment.
Emissivity test| Compliance| Electromagnetic environment — guidelines
Radio-frequency emissionsEN 55011|

Group 1

| The A500LW09 Compressor Nebuliser generates radio- frequency energy only as a consequence of internal functions. Thus, radio-frequency emission is negligible and is unlikely to cause interference in electronic devices in the surroundings of the appliance.
Radio-frequency emissions EN 55011| Class B|

The A500LW09 Compressor Nebulisercan be used in all establishments, including habitable spaces and rooms directly connected to a low-voltage mains supplying residential buildings.

Harmonic current emissions EN 61000-3-2| Class A
Voltage fluctuations/ Flicker EN 61000-3-3| Compliant

Manufacturer’s guidelines and declarations — electromagnetic immunity

The A500LW09 compressor nebuliser is intended for use in the electromagnetic environment described below.The customer or the user of the A500LW09 compressor nebuliser should ensure its use in such an environment.
Immunity tests| Test level acc. toIEC 60601| Compliance level| Electromagnetic environment— guidelines
Electrostatic discharge (ESD) EN 61000-4-2| Contact discharge±6 kVAir discharge±8 kV| Contact discharge±6 kVAir discharge±8 kV| The floor should be wooden, concrete or with ceramic tiles. If the floor is covered with synthetic material, relative humidity should be at least 30%.

Transients and burstsEN 61000-4-4

| ±2 kV for power supply lines±1 kV for input/ output lines| ±2 kV for power supply lines±1 kV for input/ output lines| The quality of the mains should correspond to the level for typical commercial or hospital environment.
---|---|---|---
SurgeEN 61000-4-5| ±1 kV lines to lines±2 kV common mode| ±1 kV differential mode±2 kV common mode| The quality of the mains should correspond to the level for typical commercial or hospital environment

Voltage dips, short interruptions and voltage variations in power supply lines EN 61000-4-11

| <5% UT (>95% UTvoltage dip) for 0.5 cycle at 40% UT (60% UT voltage dip) for 5 cycles at 70% UT (30%UT voltage dip) for 25 cycles <5% UT(>95% UT voltage dip) for 5 seconds| <5% UT (>95% UTvoltage dip) for 0.5 cycle at 40% UT (60% UT voltage dip) for 5 cycles at 70% UT (30%UT voltage dip) for 25 cycles <5% UT(>95% UT voltage dip) for 5 seconds| The quality of the mains should correspond to the level for typical commercial or hospital environment. If the user of the A500LW09 compressor nebuliser requires continuous power supply during mains outage, it is recommended to supply the A500LW09 compressor nebuliser from a UPSor batteries.
Power frequency magnetic field (50 Hz/60 Hz)EN 61000-4-8| 3 A/m| 3 A/m| The power frequency magnetic field should be at the level corresponding to typical commercial or hospital environment.
NOTE: UT stands for variable voltage of the mains before application of the test level.

Manufacturer’s guidelines and declarations — electromagnetic emissions

The A500LW09 compressor nebuliser is intended for use in the electromagnetic environment described below.The customer or the user of the A500LW09 compressor nebuliser should ensure its use in such an environment.
Immunity tests| Test level acc. to IEC 60601| Compliance level| Electromagnetic environment— guidelines
Immunity to conducted radio-frequency disturbance fields according to 61000-4-6| 3 Vrms150 kHzto 80 MHz| 3 Vrms| Portable and mobile radio communication devices should not be used near any part of the nebuliser, including cables, at thedistance less than the recommended distance calculated on the basis of an appropriate equation adapted to the frequency of the transmitter.Recommended distance.
Radio-frequency radiation according to 61000-4-3| 3 V/m80 MHzdo 2,5 GHz| 3 V/m| 80 MHz to 800 MHz
d =[ 7 ] P E 1800 MHz to 2,5 GHzwhere P is the maximum output power rating of the transmitters in watts (W) according to thetransmitter manufacturer and d is the recommended separation distance in metres (m).Field strength from fixed RF transmitters, as determined by an electromagnetic site survey, should be less than the compliance level in each frequency range.Interference may occur in the vicinity of equipment marked with the following symbol:
m

NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not apply in certain cases.

The propagation of electromagnetic waves is changed by absorption and reflection from structures, structures and humans.

• It is not possible to accurately theoretically define field strength from fixed transmitters, such as base stations for radio (cellular/wireless) telephony and terrestrial portable RF transmitters, amateur AM and RF and TV transmitters. To determine the electromagnetic conditions associated with fixed RF transmitters, measurements of electromagnetic interference at a given location shall be carried out. If the measured field strength at the location where the A500LW09 compressor nebuliser is used exceeds the applicable compliance level indicated above, the A500LW09 compressor nebuliser should be observed in order to verify the correctness of the operation. If abnormal activity is observed, additional measures may be necessary, such as repositioning or transfer of the A500LW09 compressor nebuliser.
• For the frequency range of 150 kHz to 80 MHz, field strength should be less than 3 V/m.

Recommended distance between portable and mobile radio-frequency communication devices and the A500LW09 compressor nebuliser

The A500LW09 compressor nebuliser is intended for use in the electromagnetic environment with limited interference caused by radio waves. The recipient or user of the A500LW09 compressor nebuliser can help reduce electromagnetic interference by maintaining the minimum distance between mobile RF communication devices (transmitters) and the A500LW09 compressor nebuliser according to the following recommendations, up to the maximum rated output power of the communication device

Maximum rated output power of the transmitter(W)| Distance adjusted to the frequency of the transmitter (m)
---|---
| 150 KHz to 80 MHz
| 80 MHz to 800 MHz
| 800 MHz to 2,5 GHz

0.01| 0.12| 0.12| 0.23
0.1| 0.38| 0.38| 0.73
1| 1.2| 1.2| 2.3
10| 3.8| 3.8| 7.3
100| 12| 12| 23

In the case of transmitters whose maximum rated output power is not listed above, the recommended distance d in metres (m) may be estimated using the equation suitable for the frequency of the transmitter, where P is the maximum output power rating of the transmitters in watts (W) specified by the transmitter manufacturer.

NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines may not apply in certain cases. The propagation of electromagnetic waves is changed by absorption and reflection from structures, structures and humans.

MADE FOR

 Shenzhen Aeon Technology Co. Ltd,
RM6H02, Block 27-29th, Tianxia IC Industrial Park,
Majialong No. 133 of Yiyuan road, Nantou Street,
Nanshan District, Shenzhen, China.

 Shanghai International Holding Corp. GmbH (Europe)
Eiffestrasse 80, 20537 Hamburg, Germany

Importer: Joinco Polska sp. z o.o.
ul. Cybernetyki 9
02-677 Warszawa, Polska
www.joinco.pt
Made in PRC.

Most recent version of the manual: 10.2021

References

• Joinco

Read User Manual Online (PDF format)

Download This Manual (PDF format)

Download this manual  >>