Konsung 608D User manual
Read this manual carefully before use.
Manufacture date: see the label
Product life: 5 years
ir Compressing Nebulizer
Model: 608D
User's manual
Jiangsu Konsung Bio-Medical Science and Technology Co., Ltd
A
I
Statement
Thank you for purchasing 608D air compressing nebulizer
(hereinafter referred to as "nebulizer") from Jiangsu Konsung
Bio-Medical Science and Technology Co., Ltd. (hereinafter
referred to as "Konsung).
This manual will help you understand the operation and
maintenance of the product better. It is reminded that the
product shall be used strictly complying with this manual.
User’s operation failing to comply with this manual may result
in malfunction or accident for which Konsung cannot be held
liable.
Konsung owns the copyrights of this manual. Without prior
written consent of Konsung, any materials contained in this
manual shall not be photocopied, reproduced or translated
into other languages.
Materials protected by the copyright law, including but not
limited to confidential information such as technical
information and patent information are contained in this
manual, the user shall not disclose such information to any
irrelevant third party.
The user shall understand that nothing in this manual grants
him, expressly or implicitly, any right or license to use any of
the intellectual properties of Konsung.
Konsung holds the rights to modify, update, and ultimately
explain this manual.
All illustrations in this manual serve as examples only. They
may not necessarily reflect the setup or data displayed on your
equipment.
II
Responsibility of the Manufacturer
Konsung only considers itself responsible for any effect on
safety, reliability and performance of the equipment if:
Assembly operations, extensions, re-adjustments,
modifications or repairs are carried out by persons authorized
by Konsung, and The electrical installation of the relevant
room complies with national standards, and The instrument is
used in accordance with the instructions for use.
Upon request, Konsung may provide, with compensation,
necessary circuit diagrams, and other information to help
qualified technician to maintain and repair some parts, which
Konsung may define as user serviceable. Contents of this
manual are subject to changes without prior notice.
Conventions
Warning: Indicates a potential hazard or unsafe practice that,
if not avoided, could result in death or serious
injury.
Caution: Indicates a potential hazard or unsafe practice that,
if not avoided, could result in minor personal injury
or product/property damage.
Note: Provides application tips or other useful information
to ensure that you get the most from your product.
III
Table of Contents
1 Product Introduction.........................................................1
1.1 Intended use and Contraindication...........................1
1.2 Product specification.................................................1
1.3 Structure and working principle................................3
1.4 Product features........................................................5
1.5 Equipment symbol and description.......................... 7
2 Safety Precautions............................................................ 8
3 Operating and Maintenance...........................................11
3.1 Unpacking and Inspection.......................................11
3.2 Preparations............................................................ 11
3.3 Nebulizing................................................................13
3.4 Maintenance after use............................................ 15
4 Troubleshooting Guide................................................... 17
5 Warranty and Service......................................................18
5.1 Warranty..................................................................18
5.2 Contact information................................................ 19
6 EMC..................................................................................20
6.1 Electromagnetic emissions......................................20
6.2 Electromagnetic immunity......................................21
6.3 Electromagnetic Immunity: For non-life support
equipment and systems................................................. 23
6.4 Recommended Separation Distances..................... 25
7 Parts list...........................................................................26
1
1 Product Introduction
1.1 Intended use and Contraindication
Intended use: The 608D air compressor nebulizer is
intended to aerosolize medications for inhalation by the
patient for respiratory disorders.
Contraindications: This nebulizer cannot be used for
respiratory anesthesia and ventilator systems.
Theory of operation: the respiratory system is an open
system, the liquid medicine is atomized into particles, the
patient inhalation of these drug mists, the drug mist can be
directly absorbed in the patient's mouth, throat, trachea,
bronchi, alveoli, etc. Mucosal absorption and achieve the
purpose of treatment.
1.2 Product specification
1. Maximum nebulization rate ≥0.2mL/min
2. Residual volume ≤1.3mL
3. Median particle size of 4μm, error ±25%
4. Maximum pressure of compression pump: ≥0.15MPa
5. Free flow of compression pump: ≥10L/min
6. Degree of protection against ingress of liquid: IPX0
7. Net weight: about 1.5kg (main unit only)
8. Size: about 158mmX133mmX194mm (LXWXH)
9. Power supply: Input AC220V, 50Hz
10. Pressure range of nebulizer: 60kPa to 150kPa under
normal working conditions. When an abnormality
occurs, the maximum pressure range is 150kPa to
400kPa, and no tube rupture occurs.
2
11. Equivalent volume particle size distribution curve
(measured when the solution composition is pure
water, the ambient temperature is 23°C±2°C, relative
humidity ≤80%)
12. Noise ≤58dB(A)
13. Fuse: RF1φ5×20/1.0A
14. Input power: ≤175VA
15. Electrical safety type: Class II, type B applied part
16. Safety caution: do not use this unit in environment
where combustible anesthetic gases are mixed with air,
oxygen or nitro-monoxide
17. Working mode: Continuous
18. Normal working conditions:
Environmental temperature: 5°C~35°C
Relative humidity: ≤80%
Atmospheric pressure for storage: 86kPa~106kPa
19. Restrictions on transportation and storage:
Environmental temperature: -40°C~+55°C
Relative humidity: ≤93%(non-condensing)
Atmospheric pressure: 50kPa~106kPa
Note: V means the cumulative volume distribution, and N means the cumulative volume distribution
particle size
3
NOTE:
1 Avoid violent vibration, collision and fall in transportation.
Keep the unit up, and avoid rain and gently transport.
2 Store this product in a well-ventilated and non-corrosive
gas room.
3 If the storage temperature is below 5°C, apply the device
only when the temperature meets normal operating
conditions.
1.3 Structure and working principle
Air compressing nebulizer is composed by compressor,
housing and nebulizing kit (without mask and mouthpiece).
Users can purchase masks or mouthpieces manufactured by
qualified manufacturers.
Main unit
Front view Rear view
Filter cover
* Contains
filter sheet
Holder
Air outlet
Power cord
I/O power
switch
Air inlet
4
Nebulizing assembly
Key components:
Main Structure
Material
Filter system
Felt
Compressor
Cast aluminum alloys
Electrical system
Power cord, switch, fuse
Nebulizing system
Polypropylene
Housing
ABS resin
Working principle
The compressed air generated with the pump inside the
main unit, when pumping out from the nozzle, can suck up
the medication with the negative pressure between the
nozzle and the air tube. The pumped-up medication when
impacting on the top of the septum can turn into very fine
aerosol before ejecting to the outside.
Medication cup cap
Nebulizing Kit
Medication cup
Air tube
Mask
Mouthpiece
5
Working principle block diagram:
Power supply
Compressor
Nebulizing assembly
Output
Electrical schematic:
Electrical maintenance should be operated by professionals.
1.4 Product features
1. In normal use, the atomized air flow is 3L/min to 9L/min
(flow rate is not adjustable). The corresponding pressure
is 60kPa to 150kPa.
2. The atomization volume is 2mL to 8mL, and the
theoretical atomization rate is greater than 0.2mL/min.
The corresponding pressure range is 60kPa to 150kPa.
6
3. It is recommended that the user should use a minimum
solution carrying capacity of 2mL. The maximum solution
carrying capacity should not exceed the maximum scale
of medication cup to avoid overflow. In the case of the
maximum solution carrying capacity, the maximum
temperature in the medication cup is 50°C during normal
use.
4. There is no special requirement for the type of solution.
The medication has been prescribed by the physician.
Some high concentration solutions or suspensions may
affect the nebulization rate or they are difficult to
atomize.
5. The output air pressure and flow rate is 0 under the most
unfavorable conditions.
6. Main advantages of inhalation therapy:
Inhaled medication can reach the patient respiratory
tract and lungs and deposit, this therapy is more
effective than oral drugs. Inhalation therapy is
effective and rapid in relieving bronchial asthma and
is superior to other treatments; even can save
patients life in crisis time.
As the medication reaches the respiratory tract
directly, its dosage and the toxic and side effects are
significantly reduced, ensuring the principle of
economical, affordable, effective, and safe
medication.
Dilution of mucus and sputum can be used for a
variety of respiratory diseases.
Inhalation therapy can significantly reduce symptoms
and shorten the treatment course.
Table of contents
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