Laerdal Servi Ventilator

Target SDGs

Target Users (Target Impact Group)

Small and Medium-sized Enterprises, Public Sector Agencies

Distributors / Implementing Organizations

This product was implemented by the following organizations: the Norwegian Defense Research Establishment, Edge Health Technologies AS, Laerdal Medical AS, and Servi AS.

Competitive Landscape

Direct competitors include Gradian Comprehensive Care Ventilator (CCV).

Regions

Europe

Countries

Norway, United Kingdom

Manufacturing/Building Method

The product is manufactured by Laerdal in Stavanger, Norway. The company produces components and and other products from their factories in Norway, Mexico, China, and USA.

Intellectural Property Type

Select Type

User Provision Model

The emergency ventilators are purchased by European governments to then distribute to hospitals in need.

Distributions to Date Status

1000 ventilators as of 2020

Design Specifications

The Laerdal Servi Ventilator incorporates the following components: (1) oxygen tubing and reservoir kit, (2) three 28 cm extension tubes, (3) patient valve with pressure relief valve, (4) exhalation port with a diameter of 30 mm, and (5) manometer connector. There are three consumables: (6) HME filter, (7) Thomas Tube holder, and (8) adjustable PEEP valve. The control unit allows for tidal volume adjustment between 100-800 ml and ventilation rates between 5-30 per min.

Product Schematics

Technical Support

Technical support is provided by the manufacturer.

Replacement Components

Replacement components and consumables are available for purchase from the manufacturer

Lifecycle

Unknown

Manufacturer Specified Performance Parameters

The manufacturer's goal of the rapid-development project emphasized quick production, simple to use, and simplified (but accurate) automated assisted breathing.

Vetted Performance Status

The system has been tested with test lungs to in both controlled and assisted ventilation mode, details of the performance testing and design iterations are available in the FFI report.

Safety

The product has been designed and tested to meet patient safety standards in Norway.

Complementary Technical Systems

None

Academic Research and References

Compliance with regulations

Received the European CE (Communauté Européenne) Mark

Evaluation methods

Unknown

Other Information

None