PCI Deployable Oxygen Concentration Systems

Target SDGs

Market Suggested Retail Price

$163,800.00

Target Users (Target Impact Group)

Distributors / Implementing Organizations

None

Competitive Landscape

Direct competitors include Solar-Powered Oxygen Delivery (SPO2) and O2 Cube.

Manufacturing/Building Method

PCI manufactures its products in production facilities in California, USA; Curitiba, Brazil; and Bangalore, India.

Intellectural Property Type

Patent

User Provision Model

Direct sales to hospitals and medical centers

Distributions to Date Status

As of 2020, this product has been installed in over 100 medical facilities worldwide.

Design Specifications

This produce uses Vacuum Swing Adsorption (VSA oxygen) technology to collect, compress, and supply oxygen to a medical clinic. This product is designed to be "plug and play" and function automatically. Connection is made into the hospital oxygen pipeline to major users (e.g., ICU, ER, OP) in permanent or temporary situations. Medical oxygen is then supplied on-demand with flow adjustment from 25 - 100% of system capacity.

Product Schematics

Technical Support

Provided by the manufacturer

Replacement Components

Provided by the manufacturer

Lifecycle

15-20 years

Manufacturer Specified Performance Parameters

The manufacture designed this product to be automatic, portable, and durable for emergency settings.

Vetted Performance Status

This product has been vetted by the manufacturer to comply with the following performance standards:

• Oxygen 93% USP & PH.EUR
• ISO 7396-1:2016
• ISO 9001 & 13485
• EU Medical devices directive Class IIb Council Directive 93/42 EEC
• 006/42 EC Machinery Directive
• 97/23/EEC Pressure Equipment Directive (PED)
• 2006/95/EC, Low Voltage Electrical Equipment Directive (LVD)

Safety

Unknown

Complementary Technical Systems

The system connects to clinical equipment that requires an oxygen supply.

Academic Research and References

Compliance with regulations

The device complies with ISO 7396-1:2016, ISO 9001 & 13485, EU Medical devices directive Class IIb Council Directive 93/42 EEC, 006/42 EC Machinery Directive, 97/23/EEC Pressure Equipment Device (PED), and 2006/95/EC Low Voltage Electrical Equipment Directive (LVD).

Evaluation methods

Unknown

Other Information

None