Shanghai Berry Electronic Tech Co., Ltd.
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Product Facts
Fully shielded patient cable and lead wires
High density interface allows compact size,light weight
Keyed lead wire termination to provide correct o rientation
Latex-free
Instrument Connectors
An extensive variety of connector solutions is available.All have flex-reliefs for durability.
Lead wires
Low profile,insert molded snap or pinch connectors offer patient comfort and secure attachment
to snap electrodes.The snap termination’s ergonomic,teardrop design reduces tangling at the patient
end connector.Grabber and mini clip terminations have dual sided metal contacts to provide the connection.
Specification
Storage and transport environment:-5--+40
Operating temperature:0--+40
Humidity
Operating/Storage/Transportation 0% to 80% non condensing Altitude
Hyperbaric Pressure 86kPa—106k Pa
Biocompatiblity:All patient contact materials are latex free and have been tested according to ISO 10993-5,ISO10993-10.
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.
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.