1. Air compressing nebulizer is developed for the successful treatment of asthma ,

allergies and other respiratory disorders .

2. It creates a stream of air that travels through clear air tube to the medicine cup.

3. When air enters the medicine cup ,

it will convert the prescribed medication into aerosol mist for easy inhalation.

Introduction

   This equipment sprayed liquid medication to fog panel by compressing air,and form tiny particles,which flow into the throat
through imbibing tube.It adopts oil-free-high-efficiency valve with no need for daily lubrication and it is with low noise,tiny
particles.

TECHNICAL FEATURES

- Extreme Pressure: approx. 2.7 bar

- Free Flow: approx. 12.5 L/min

- Nebulizing Rate: approx. 0.35 ml/min

- Particle Size(MMAD): approx. 3.4 μm

- Fine Particle Fraction(FPD): approx. 70%

- Noise Level: approx. 55 dB

- Max capacity of nebulizer kit: 10 mL

- Operating mode: Continuous Use

- Pump life: 2000 hours

- Weight: 1.4 Kg

- Size: 280mm x180mm x 88mm

Factory

Industrial automation is an important prerequisite for starting Industry 4.0, BERRY as the industry leader,is keeping pace with the trend of the times.we have been implementing automation on our core technology and became the creator of advanced manufacture technology in the industry.

Why Choose Us

Shanghai Berry Electronic Tech Co., Ltd. is located in Shanghai Caohejing High-tech Park, a beautiful low-carbon and environmentally friendly city. We have been devoted to the R&D, manufacturing and sales of medical electronic instruments in the field of monitoring since 2003.

Our Bio-Medical technology has reached the domestic advanced level. Important breakthroughs have been made in non-invasive blood pressure calculation methods, blood oxygen saturation detection, and multi-parameter monitoring systems. After years of development, we have established good cooperative relations with customers worldwide, with annual sales reaching tens of millions dollars.

BERRY always provides customers with high-quality, cost-effective products. It is important for us to maintain good quality.
In 2009, we obtained the production license and product registration certificate that issued by Shanghai.
ln 2014, we passed the EN ISO 13485 quality system certification and CE0123 certification by TÜV SÜD. And we got the 510K for the wrist and handheld pulse oximeter
ln 2015, we got ANVISA, INMETRO Approved.
In 2016, we got FDA510K approved for fingertip pulse oximeter.
In 2018, we got CE0123 approved for Patient Monitor and new watch oximeter
In 2019, we established Shenzhen factory.
In 2022-now, our business growing up rapidly, and have more cooperation partners.