beurer IH 28 Pro Inhalator Instruction Manual

June 15, 2024
Beurer

IH 28 Pro

beurer IH 28 Pro Inhalator

beurer IH 28 Pro Inhalator Nebuliser
Instructions for use

Unfold page 3 before reading the instructions for use.

beurer IH 28 Pro Inhalator - Figure 1

Read these instructions for use carefully and keep them for later use. Make them accessible to other users and note the information they contain.

INCLUDED IN DELIVERY

Check that the exterior of the cardboard delivery packaging is intact and make sure that all contents are present. Before use, ensure that there is no visible damage to the device or atomiser set (= year pack) and that all packaging material  has been removed. If you have any doubts, do not use the device and contact your retailer or the specified
Customer Service address.
See description of device and atomiser set
1 x nebuliser
1 x atomiser
1 x compressed air hose
1 x mouthpiece
1 x silicone adult mask (size M)
1 x silicone children’s mask (size S)
1 x angled fitting
1 x nosepiece with comfort attachment
1 x nasal douche
10 x replacement filter
1 x set of these instructions for use

SIGNS AND SYMBOLS

The following symbols are used on the device, in these instructions for use, on the packaging and on the type plate for the device:

| Warning
Warning indicating a risk of injury or damage to your health
---|---
| Important
Safety note indicating possible damage to the device/atomiser set
**| Product information
Note on important information
| Application part, type BF
| Observe the instructions for use
| Protection class 2 device
| Manufacturer
I| On
O| Off
30 min. ON /30 min. OFF| 30 minutes of operation, then 30 minutes break before operating again.
IP21**| Protected against foreign objects ≥ 12.5 mm and against vertically falling drops of water
| This product satisfies the requirements of the applicable European and national directives.
| Separate the packaging elements and dispose of them in accordance with local regulations.
| Marking to identify the packaging material.
A = material abbreviation,
B = material number:
1–7 = plastics,
20–22 = paper and cardboard
| Separate the product and packaging elements and dispose of them in accordance  with local regulations.
| Disposal in accordance with the Waste Electrical and Electronic Equipment EC Directive (WEEE)
| Date of manufacture
| Permissible storage and transport temperature and humidity
| Medical device
| Unique device identifier (UDI)
Identifier for unique product identification
| Item number
| Serial number
| Single patient – multiple use
| Do not dispose of batteries containing harmful substances with household waste

INTENDED USE

Purpose
Nebulisers (including compressor, ultrasonic and mesh nebulisers) are medical devices for the nebulisation of liquids and liquid medication (aerosols). This device produces aerosols by combining compressed air and liquid medication. The aerosol treatment is suitable for treating the upper and lower airways. By nebulising and inhaling the medication prescribed/recommended by your doctor, you can prevent diseases affecting the airways, or in the case that you contract such an illness, you can alleviate symptoms and speed up your recovery.

Target group
The nebuliser is only intended for medical care in a home environment. The nebuliser is not intended for health care in professional environments. The nebuliser can be used on anyone over 2 years of age under supervision; it can be used for self-treatment by anyone over 12 years of age.
The shape of the person’s face determines whether or not the device can be used under supervision. As such, it may be possible to use the device under supervision on someone who is younger, or conversely it may not be possible to use  the device until they are older. When using a mask to inhale, take care to ensure the mask fits well and the eyes are unobstructed.
Clinical benefits
Inhalation is the most effective way to administer medication for most respiratory system conditions.

The benefits are:

  • The medication is transported directly to the target organs,
  • The local bioavailability of the medication is significantly increased,
  • Systemic diffusion is reduced substantially,
  • Only very low doses of the medication are required,
  • Quick and effective therapeutic effect,
  • Side effects are significantly reduced compared to systemic administration,
  • Humidifying of the airways,
  • Loosening and making (bronchial) secretions more liquid,
  • Releasing bronchospasms (spasmolysis),
  • Relieving swollen and inflamed bronchial mucosa,
  • Coughing up secretions,
  • Fighting viruses that affect the upper and lower airways.

Indication

The nebuliser can be used for diseases of the upper and/or lower airways. Examples of upper respiratory system diseases include:

  • Rhinitis,
  • Allergic rhinitis,
  • Sinusitis,
  • Pharyngitis,
  • Laryngitis.
  • Examples of lower respiratory system diseases include:
  • Bronchial asthma,
  • Bronchitis,
  • COPD (chronic obstructive pulmonary disease),
  • Bronchiectasis,
  • Acute tracheobronchitis,
  • Cystic fibrosis,
  • Pneumonia.

Contraindications

  • The atomiser is not intended for the treatment of life-threatening conditions.
  • This device must not be used by children under the age of 12 and by people with reduced physical, sensory (e.g. reduced sensitivity to pain) or mental skills or a lack of experience or knowledge, unless they are supervised or have  been instructed on how to use the device safely, and are fully aware of the consequent risks of use.
  • Do not use the device on persons who are ventilated and/or unconscious.
  • Check whether there are contraindications for use with the usual systems for aerosol treatment on the medication instruction leaflet.
  • If the device does not work properly, or if you feel unwell or experience pain, stop using it immediately.

WARNINGS AND SAFETY NOTES

Warning

  • The atomiser has no significant influence on the efficacy and safety of the medication administered and is not intended for the treatment of life-threatening conditions.
  • If the device malfunctions, please refer to the “What if there are problems” section.
  • The device is not a substitute for medical consultation and treatment. Always consult your doctor first in the event of pain or illness.
  • If you have health concerns of any kind, consult your GP!
  • If the liquid you wish to use is not compatible with PP, silicone and PVC, do not use this liquid with our nebuliser. If the information provided with the liquid does not indicate whether the liquid is compatible with these materials, please contact the liquid manufacturer.
  • Please observe the general hygiene measures when using the atomiser.
  • You should always follow the instructions of your doctor regarding the type of medication to use, the dosage, and the frequency and duration of inhalation.
  • Only use medication prescribed or recommended by your doctor or pharmacist.
  • For treatment, only use parts indicated by your doctor according to the particular diagnosis.
  • Keep the device away from your eyes when it is in use, as the mist of medication could be harmful.
  • Do not operate the device in the presence of flammable gases or if there is a high oxygen concentration.
  • The device must be switched off and the plug pulled out before every cleaning procedure.
  • Keep packaging material away from children (risk of suffocation).
  • Under no circumstances should you open or repair the device yourself, otherwise proper functionality can no longer be guaranteed. Failure to comply will invalidate the warranty.
  • The device is only intended for domestic/private use, not for commercial use.
  • Children must not play with the device.
  • To avoid the risk of entanglement and strangulation, store cables and air lines out of the reach of small children.
  • Do not use any additional parts that are not recommended by the manufacturer.
  • The device must only be connected to the mains voltage that is specified on the type plate.
  • Never submerge the device in water and do not use it in the bathroom. Under no circumstances may liquid enter the device.
  • Protect the device from heavy impacts.
  • Never touch the mains cable with wet hands, as you could get an electric shock.
  • Do not pull the mains plug out of the socket using the mains cable.
  • Do not crush or bend the mains cable, pull it over sharp-edged objects or leave it dangling down, and protect it from sources of heat. Do not wrap the mains cable around the device, either during storage or use.
  • We recommend that the mains cable is completely unrolled to avoid dangerous overheating.
  • If the mains cable of this device is damaged, the device must be disposed of.
  • If the device is opened, there is a risk of electric shock. Disconnection from the power supply network is only guaranteed if the mains plug is unplugged.
  • Modification of the device and atomiser set is not permitted.
  • If the device has been dropped, exposed to high levels of moisture or suffered any other damage, it must no longer be used. If in doubt, contact Customer Services or the retailer.
  • The nebuliser may only be operated with compatible Beurer atomisers and with the appropriate Beurer atomiser set. The use of atomisers and atomiser sets made by other companies may result in less efficient treatment and could damage the device.
  • Store the device and atomiser set out of the reach of children and pets.

Important

  • Power cuts, sudden interferences or other unfavourable conditions could lead to the device becoming inoperable. We therefore recommend that you obtain a replacement device or medication (the latter should be agreed with your  doctor).
  • Should you require an adapter or extension lead, this must meet the applicable safety requirements. The power limit and the maximum output specified on the adapter must not be exceeded.
  • Never store the device or the mains cable near to sources of heat.
  • Do not use the device in a room in which a spray has previously been used. Air the room before carrying out the treatment.
  • Do not allow objects to get into the cooling vents.
  • Never use the device if it is making an abnormal sound.
  • For hygiene reasons, it is essential that every user uses their own atomiser set.
  • Always disconnect the mains plug from the mains socket after use.
  • Store the device in a location protected against climatic influences. The device must be stored in the environmental conditions specified.

FUSE

  • The device is fitted with an overcurrent protection device. This may only be replaced by authorised specialist personnel.

General notes
Important

  • The device is suitable only:
    – on people
    – for the purpose for which it is designed (aerosol inhalation) and in the manner specified in these instructions for use.

  • Any form of improper use can be dangerous!

  • In the event of an acute emergency, providing first aid must take top priority.

  • Apart from the medication, only use distilled water or a saline solution. Other liquids may cause a fault in the nebuliser or atomiser.

Prior to initial use
Important

  • Remove all packaging material before using the device.
  • Protect the device against dust, dirt and humidity and never cover the device while it is in use.
  • Do not operate the device in a very dusty area.
  • Switch the device off immediately if it is faulty or not working properly.
  • The manufacturer is not liable for damage resulting from improper or incorrect use.
  • This device is not intended for commercial or clinical use; it is designed exclusively for self-treatment in a private home.

Repairs
Notice

  • Under no circumstances should you open or repair the device yourself, otherwise proper functionality can no longer be guaranteed. Failure to comply with this instruction will void the warranty.
  • The device is maintenance-free.
  • For repairs, please contact Customer Services or an authorised retailer.

DEVICE AND ATOMISER SET DESCRIPTION

Nebuliser
The corresponding drawings are shown on page 3.

  1. Mains connector cable

  2. Lid

  3. On/Off control

  4. Compartment for atomiser set

  5. Filter cap with filter

  6. Hose connection

  7. Holder for atomiser
    Atomiser and atomiser set

  8. Compressed air hose

  9. Atomiser

  10. Atomiser insert

  11. Valve

  12. Medication container

  13. Mouthpiece

  14. Silicone adult mask

  15. Silicone children’s mask

  16. Nosepiece with comfort attachment

  17. Replacement filter

  18. Angled fitting

  19. Nasal douche
    Nasal douche

  20. Cover

  21. Collection container for nasal secretion

  22. Saline container

  23. Cover hole

INITIAL USE

Setting up the device
Take the device out of the packaging.
Place the device on a flat surface.
Make sure that the vents are free from obstructions. Open the lid 2 to access the parts of the atomiser set.

Before using the device for the first time
Notice

  • Clean and disinfect the atomiser and atomiser set before using them for the first time. See “Cleaning and maintenance” in this regard.
  • Connect the compressed air hose 8 to the bottom of the medication container 12 . A 1
  • Connect the other end of the compressed air hose 8 to the nebuliser hose connection 6 by turning it slightly. A 2
  • Insert the medication container 12 into the holder for the atomiser 7

Mains adapter connector
The device must only be connected to the mains voltage that is specified on the type plate.

  • Insert the mains plug of the mains cable 1 into a suitable socket.
  • To connect to the mains, fully insert the plug into the socket.

Notice

  • Ensure that there is a mains socket close to the set-up area.
  • Arrange the mains cable so that no-one will trip over it.
  • To disconnect the nebuliser from the mains after inhalation, first switch off the device and then pull the mains plug out of the socket.

USAGE

Important

  • For hygiene reasons, it is essential to clean the atomiser 9 and the rest of the atomiser set after each treatment and to disinfect them after the last treatment of the day.
  • The atomiser set parts may only be used by one person; use by several people is not recommended.
  • If the therapy involves inhaling several different medications one after the other, please be aware that the atomiser 9 must be rinsed under warm tap water following every usage. See “Cleaning and maintenance” in this regard.
  • Please observe the notes on changing the filter in these instructions for use.
  • Check that the hose connectors are firmly attached to the nebuliser 6 and the atomiser 9 before each use of the device.
  • Before use, check that the device is functioning correctly. To do this, briefly switch on the nebuliser (together with the connected atomiser, but without medication). If air comes out of the atomiser 9 , the device is working.

7.1 Inserting the atomiser insert

  • Open the atomiser 9 by twisting the top anticlockwise against the medication container 12 . Place the atomiser insert 10 in the medication container 12.
  • Ensure that the cone for administering medication fits well on the cone for the air duct inside the atomiser 9 .

7.2 Filling the atomiser

  • Fill with an isotonic saline solution or pour the medication directly into the medication container 12 . Avoid overfilling. The maximum recommended filling quantity is 8 ml.
  • Use medication only as instructed by your doctor and ask about the appropriate inhalation period and quantity for you.
  • If the prescribed quantity of medication is less than 2 ml, top this up to at least 4 ml with isotonic saline solution. Dilution is also necessary with viscous medications.
    Here too, please observe the instructions of your doctor.

7.3 Closing the atomiser

  • Close the atomiser 9 by twisting the top clockwise against the medication container 12 . Ensure that the connection is correct.

7.4 Inserting the valve

  • Press the valve 11 into the opening intended for this purpose on the upper side of the atomiser 9.

Notice
Only use the valve 11 with the mouthpiece 13 . Never use it with the masks 14 15 and never with the nosepiece 16 .

7.5 Connecting the atomiser set to the atomiser

  • Connect the atomiser 9 to the desired atomiser set (mouthpiece 13 , silicone adult mask 14 , silicone children’s mask 15 or nosepiece 16 ).

Notice
The most effective form of nebulisation is by using the mouthpiece. Nebulisation using a mask is only recommended if it is not possible to use a mouthpiece (e.g. for children who are not yet able to inhale using a mouthpiece).
When using a mask to inhale, take care to ensure the mask fits well and the eyes are unobstructed.

  • Before the treatment, pull the atomiser upwards out of the holder 7.
  • Start the nebuliser using the On/Off control 3 .
  • Spray mist pouring out indicates that the device is operating correctly.

7.6 Treatment

  • When inhaling, sit upright and relaxed at a table and not in an armchair to avoid compressing the airways and therefore impairing the effectiveness of the treatment.
  • Breathe in the atomised medication deeply.

Important
The device is not suitable for continuous operation; after 30 minutes of operation it must be switched off for 30 minutes.
Notice
During the treatment, hold the atomiser straight (vertically), otherwise the atomisation will not work and faultless functionality is not guaranteed.
Important
Essential oils, cough syrups, gargling solutions and drops to be used as a rub or in a steam bath are wholly unsuitable for inhalation using a nebuliser.
These additives are often viscous and can impair the correct functioning of the device and therefore the effectiveness of the application in the long term. For individuals with a hypersensitive bronchial system, medications containing  essential oils may under certain conditions cause an acute bronchospasm (a sudden cramp-like restriction of the bronchi with shortness of breath). Consult your doctor or pharmacist in relation to this matter.
7.7 Stopping the inhalation
Once the mist is only coming out in an irregular flow or if the sound changes when inhaling, you can stop the treatment.

  • Switch off the nebuliser after treatment using the On/Off control 3 and disconnect it from the mains.
  • Place the atomiser 9 back in its holder 7 after the treatment.

7.8 Nasal douche
You can use the nasal douche to clean your nasal cavities. The nasal douche creates a fine jet of liquid for treating respiratory tract problems or for moistening the nasal mucous membranes.
We recommend using the nasal douche for colds, dryness inside the nose, dust exposure, pollen allergies, chronic inflammation of the sinuses or upon the advice of your doctor.

Warning

  • Do not use the nasal douche in combination with other medication or essential oils.

Important

  • Only use the nasal douche with isotonic saline solutions.
  • Replace the nasal douche after a year.
    The maximum volume of the nasal douche is 10 ml.
    If you are unsure about the correct dilution of the saline solution, please consult your pharmacist.

7.9 Using the nasal douche
To use the nasal douche correctly, proceed as follows B :

  1. Twist the cover 20 90° anticlockwise and remove it in an upward direction.

  2. Also lift the collection container 21 out.

  3. Fill the saline container 22 with saline solution.

  4. Place the collection container 21 into the saline container 22 .

  5. Place the cover 20 on the saline container 22 .
    Twist the cover 20 in a clockwise direction until it clicks firmly into place.

  6. Connect the compressed air hose 8 to the saline container 22 from below.

  7. Carefully position the cover 20 in one of your nostrils. Breathe through your nose.

  8. Press the On/Off control 3 . To start the application, place one finger over the cover hole 23 on the container.
    Notice
    During the application, breathe slowly and evenly through your nose. Tilt your head slightly in the opposite direction to the nostril being treated so that the saline solution can flow deep into the nose.

  9. To pause or stop the application, take your finger off the cover hole 23 on the saline container 22.

  10. Once your nose feels clear again, you can stop the application. The application should be stopped at the latest once the maximum filling quantity has been used.

7.10 Cleaning
See “Cleaning and maintenance”.

CHANGING THE FILTER

In normal operating conditions, the air filter must be replaced after approx. 200 operating hours or one year. Please check the air filter regularly (after 10-12 nebulisation procedures). Replace the used filter if it is very dirty or clogged. If  the filter has become damp, it must also be exchanged for a new filter.
Important

  • Do not attempt to clean the used filter and reuse it.
  • Only use the manufacturer’s original filter, otherwise your nebuliser may become damaged and sufficiently effective treatment cannot be guaranteed.
  • Do not repair or maintain the air filter while it is in use.
  • Never operate the device without a filter.

To replace the filter, proceed as follows:
Important

  • First switch the device off and disconnect it from the mains.
  • Allow the device to cool down.
    1. Remove the filter cap 5 upwards. C
    Notice
    If the filter remains in the device after the cap has been removed, take the filter out of the device, e.g. with tweezers or similar.
    2. Re-insert the filter cap 5 with a new filter.
    3. Ensure that it is securely in place.

CLEANING AND MAINTENANCE

Atomiser and atomiser set
Warning
Adhere to the following hygiene instructions to avoid health risks.

  • The atomiser 9 and the rest of the atomiser set are intended for multiple use. Please note that different areas of application involve different requirements in terms of cleaning and hygienic preparation.

Notice

  • Do not clean the atomiser or the atomiser set mechanically using a brush or similar device, as this could cause irreparable damage and it will mean that the best treatment results can no longer be guaranteed.
  • Please consult your doctor about the additional requirements in terms of the hygienic preparation needed (hand care, handling of medication/inhalation solutions) for high-risk groups (e.g. patients with cystic fibrosis).
  • Ensure thorough drying after each cleaning and disinfection process. Residual moisture or wetness can represent an increased risk of bacterial growth.

Preparation

  • Immediately after each treatment, all parts of the atomiser 9 and the rest of the atomiser set used must be cleaned of medication residues and contamination.
  • To do this, dismantle the atomiser 9 into its individual parts.
  • Remove the mouthpiece 13 , mask 14 15 or nosepiece 16 from the atomiser.
  • Disassemble the nosepiece if you have used it with the comfort attachment.
  • Dismantle the atomiser by twisting the top anticlockwise against the medication container 12 .
  • Remove the atomiser insert 10 from the medication container 12.
  • Remove the valve 11 by pulling it out of the atomiser 9 .
  • Reassembly is carried out in reverse order.

Cleaning
Important
The device must be switched off, disconnected from the mains and allowed to cool down each time before cleaning.
The atomiser 9 and the rest of the atomiser set used, such as the mouthpiece 13 , masks 14 15 , atomiser 9 , nasal douche 19 , etc. must be cleaned with hot but not boiling water after each use. Dry the parts carefully using a soft cloth. Put  the parts together again when they are completely dry and place them in a dry, sealed container or disinfect them.
When cleaning, ensure that any residue is removed. Never use any substances for cleaning that could potentially be toxic if they came into contact with the skin or mucous membranes, or if they were swallowed or inhaled.
Use a soft, dry cloth and non-abrasive cleaning products to clean the device.
Do not use any abrasive cleaning products and never submerge the device in water.

Important

  • Make sure that no water gets inside the device!
  • Do not clean the device or atomiser set in the dishwasher!
  • Do not touch the device with wet hands when it is plugged in and do not allow water to spray on the device. Only operate the device if it is completely dry.
  • Do not spray any liquid into the vents! If liquid penetrates the device this could cause damage to the electrics or other nebuliser parts and lead to a malfunction.

Condensation, hose care
Condensation may form in the hose depending on the ambient conditions. It is essential to remove the moisture to prevent bacterial growth and ensure proper treatment.
To do so, proceed as follows:

  • Disconnect the hose 8 from the atomiser 9 .
  • The hose must remain in the nebuliser 6 .
  • Operate the nebuliser until the moisture is removed by the air passing through.
  • In the event of heavy contamination, replace the hose.

Disinfection
Please carefully observe the points below when disinfecting your atomizer and the atomizer set.
We recommend disinfecting the individual parts on a daily basis after the last usage as a minimum measure.

  • First, clean the atomiser and atomizer set as described in the “Cleaning” section.
  • Place the disassembled atomiser 9 , nasal douche 19 , mouthpiece 13 , the silicone masks 14 15 and the disassembled nosepiece 16 in boiling water for 5 minutes. Contact between the parts and the hot base of the pan should be avoided.
  • For disinfection immerse the compressed air hose in a 2 % sodium hypochlorite (NaOCl) solution for 15 minutes (i.e. a solution made from the disinfecting agent Amuchina® or a 2  % sodium hypochlorite solution mixed by your  pharmacist). Afterwards rinse all parts thoroughly with tap water, to fully remove any possible residue of the disinfectant solution.

Storage

  • Do not store in damp conditions (such as in a bathroom) and do not transport with any damp items.
  • When storing and transporting, protect from prolonged direct sunlight.
  • The parts of the atomiser set can be securely stored in the storage compartment 4. Store the device in a dry place, ideally in the original packaging.

ATOMISER SET AND REPLACEMENT PARTS

The atomiser set parts and replacement parts are available from the corresponding service address (according to the service address list). Please state the corresponding order number.

Designation Material REF

Atomiser set = year pack
includes:
Mouthpiece
Nosepiece
Silicone adult mask
Silicone children’s mask
Atomiser
Compressed air hose
Filter
Angled fitting| PP/silicone
PP/silicone
Silicone/PP
Silicone/PP
PP/silicone
PVC
PU
PP| 603.76
Nasal douche| PP| 601.37

Notice

If the device is not used according to the specifications, perfect functionality cannot be guaranteed! We reserve the right to make technical changes to improve and develop the product. This device and its atomiser set conform with the European standard EN 60601-1-2 (Group 1, class B, in accordance with CISPR 11, IEC  61000-3-2, IEC  61000-3-3, IEC  61000-4-2, IEC 61000-4-3, IEC  61000-4-4, IEC  61000-4-5, IEC  61000-4-6, IEC  61000-4-7, IEC 61000-4-8, IEC 61000-4-11) and is subject to particular precautions with regard to electromagnetic compatibility.

Please note that portable and mobile HF communication systems may interfere with this device.
For more details, please contact our Customer Services at the address indicated.

Notes on electromagnetic compatibility

  • The device is suitable for use in all environments listed in these instructions for use,  including domesticenvironments.
  • The use of the device may be limited in the presence of electromagnetic disturbances. As a result, the device may fail.
  • Avoid using this device directly next to other devices or stacked on top of other devices, as this could lead to faulty operation. If, however, it is necessary to use the device in the manner stated, this device as well as the other devices must be monitored to ensure they are working properly.
  • The use of an atomiser set other than that  specified or provided by the manufacturer of this device can lead to an increase in electromagnetic emissions or a decrease in the device’s electromagnetic immunity; this can result in faulty operation.
  • Keep portable RF communication devices (including peripheral equipment, such as antenna cables or external antennas) at least 30 cm away from all device parts, including all cables included in delivery.
  • Failure to comply with the above could impair the performance of the device.

WHAT IF THERE ARE PROBLEMS?

Problems/ questions Possible cause/remedy
The atomiser produces no or too little aerosol. 1.Too much or too little

medication in the atomiser.
Minimum: 2 ml,
Maximum: 8 ml.
2.Check nozzle for blockages.
Clean nozzle if necessary (e.g. by rinsing out). Then start using the atomiser again.
IMPORTANT: Carefully pierce the fine holes only from the underside of the nozzle.
3.Atomiser not held vertically.
4.Unsuitable medication fluid added for nebulisation (e.g. too  viscous).
The medication fluid should be prescribed by a doctor.
The output is too low.| Kinked hose, clogged filter, too much inhalation solution.
---|---
What med- ications are suitable for inhaling?| Please consult your doctor in relation to this matter.
As a rule, all medication that is suitable and approved for device inhalation can be inhaled.
There is inhalation solution residue in the atomiser.| This is normal and is due to tech-nical reasons. Stop inhalation once the atomiser starts to make a notably different sound.
What should be taken
into account when using the device with chil- dren?| On children, the mask should cover the mouth and nose to en-sure effective inhalation. It is not very useful to carry out nebulisation on someone who is sleeping, as in this case not enough of the medication will reach the lungs.
Notice: Inhalation should only be carried out under the supervision of an adult and with their assistance and the child should not be left alone.
Why should the atomiser be replaced regularly?| There are two reasons for this:
1.To ensure a therapeutically effective particle spectrum, the nozzle hole must not exceed a specific diameter. Due
to mechanical and thermal stresses, the plastic is subject to a certain degree of wear. The atomiser insert is
particularly delicate. This can also alter the composition of the aerosol droplets, which directly affects the effectiveness of the treatment.
2.Regularly changing the atomiser is also recommended for hygiene reasons.
Should each person have their own atomiser?| Yes, this is absolutely essential for hygiene reasons.

DISPOSAL

For environmental reasons, do not dispose of the device in the household waste.
Please dispose of the device in accordance with EC Directive – WEEE (Waste Electrical and Electronic Equipment).
If you have any questions, please contact the local authorities responsible for waste disposal.

TECHNICAL SPECIFICATIONS

Model IH 28 Pro
Type IH 28
Dimensions (W x H x D) 210 x 210 x 94 mm
Weight 1.65 kg
Operating pressure Approx. 0.5 to 1.45 bar
Atomiser filling volume Max. 8 ml Min. 2 ml
Medication flow rate Approx. 0.35 ml/min
Sound pressure Approx. 52 dBA
Mains connection 230 V-; 50 Hz; 230 VA

UK: 240 V-; 50 Hz; 240 VA
Operating conditions| Temperature: +10 °C to +40 °C Relative humidity: 15% to 93% Ambient pressure:
700 to 1060 hPa
Storage and transportation conditions| Temperature: -25°C to +70°C Relative humidity: 10% to 95% Ambient pressure:
700 hPa to 1060 hPa
Aerosol values accord-
ing to EN
27427:2019 based on adult breathing patterns with sodium fluo- ride (NaF):| 1) Aerosol delivery: 0.11 ml
2) Aerosol delivery rate: 0.07 ml/min
3) Fill volume dispensed in per-cent per min. 3.5%
4) Residual volume: 1.68 ml
5) Particle size (MMAD): 3.07 pm
6) GSD (geometrical standard deviation): 2.03
7) RF (respirable fraction c 5 pm): 75%
8) Large particle range (>5 pm): 25%
9) Medium particle range (2 to 5 pm): 47.8%
10) Small particle range (<2 pm): 27.2%

The serial number is located on the device or in the battery compartment.
Subject to technical changes.

Particle size diagram

Measurements were performed using a sodium fluoride solution with a “Next Generation Impactor” (NGI).
The diagram may therefore not be applicable to suspensions or highly viscous medications. You can obtain more detailed information from the manufacturer of your medication.

WARRANTY/SERVICE

Further information on the warranty and warranty conditions can be found in the warranty leaflet supplied.
Notification of incidents
For users/patients in the European Union and identical regulation systems (EU Medical Device
Regulation (MDR) 2017/745), the following applies:
If a major incident occurs during or through use of the product, notify the manufacturer and/or their representative of this as well as the respective national authority of the member state in which the you are located.

Beurer GmbH Söflinger Str. 218  89077 Ulm, Germany www.beurer.com
www.beurer-gesundheitsratgeber.com  www.beurer-healthguide.com

References

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