Ultrasonic aerosol device PM22, Perfect Medical

• Intended users: Adult and pediatric patients suffering from asthma, chronic obstructive pulmonary disease (COPD), such as emphysema and chronic bronchitis, or other respiratory diseases characterized by airflow obstruction.
• The device is intended for home, hospital use.
• This ultrasonic nebulizer is designed for the treatment of the upper and lower respiratory tract. Liquid medication converted by high-frequency vibrations into droplets, at a predominant droplet size of 1 - 5 µm, can reach the lower respiratory tract.
• It is effective for the treatment of lung disorders, tracheitis, bronchial asthma, sinusitis and allergies. Moreover, it can alleviate the disorders caused by colds and allergic irritations and alleviate the stimulus of cough, pain and the feeling of compression in the area of ​​the paranasal sinuses.
• The advantage of aerosol therapy is that drugs are delivered directly through the mouth or through the nose and throat into the lungs without having to pass through other organs first. The effects are noticeably fast and the use of drugs is minimal.
• Follow the doctor's instructions for the type of medicine to be used, the dose, frequency and duration of inhalation treatments.
• This ultrasonic nebulizer is intended for human use only and should only be used for its intended purpose as described in the instructions for use.

Technical specifications:
Supply voltage:
Input: 100-240V AC, 50-60Hz, 0.4A
Output: DC 13.5V, 1A
Operating conditions:
Temperature: Min. 5 °C; max. 40 °C
Relative humidity : Less than 85%

Storage conditions:

- Temperature: Min. -25 °C; max. 70 °C
- Relative humidity: Less than 95%

Product specifications:

- Ultrasound frequency: 1.7 MHz
- Nebulization flow: approx. 0.4 ml/minute
- Aerosol inhalation percentage: 60% of particles < 5 μm
- Particle size: 4.8 μm
- Nebulization capacity: Max. 10 ml = 10 cc
- Atmospheric pressure: 860 hPa ~ 1060 hPa
- Size: 130 x 84 x 120 mm
- Weight: 368 ±15g

This device and its accessories comply with the European Directive 93/42/EEC for medical devices and also comply with the following European safety, EMC and performance standards: EN60601-1, EN60601-1-2, EN13544-1