Trionara Technologies AB. founded in 2010 in Sweden with main business focus in production, marketing and sale of medical devices mainly including Patient Care monitors with Central Monitoring System under brand name of “ViTUS”.

Later on the company expands its portfolio with Electrocardiograph device and ICU Ventilators.   

Company Structure

Trionara structure breaks down into 5 main departments as:

•        Marketing & sale

•        Production

•        Business development

•        After sales services and

•        Quality assurance/control

 

Company History

Trionara has been set up in 2010 and gradually built its reputation as a trading company in Sweden. Achieving successful result in marketing and sale made Trionara develop a new strategy of acquiring OEM medical device technology with the purpose of localizing and deploying it in Sweden and toward the aim of worldwide expansion of target market in Europe, Asia, South America, Africa and rest of countries.

The new strategy has been implemented by setting up assembly line of the medical device for being recognized and accredited as a medical device manufacturer.

 

Vision

Trionara Technologies strives for excellence to further enhance its position and being recognized as one of medical device role player in global highly demanding markets of healthcare industry by targeting different regions from Europ, Asia, and Middle East to South America and Africa.

Trionara aims at moving aligned with novel and revolutionary technology through monitoring new trends of medical device market and increasing investment in research and development of innovative technologies.

 

Mission

Trionara moves forward its vision by following best business practices and delivering highly quality, safe and reliable products to fulfill customer needs and satisfaction thought providing best medical care solutions in compliance with market regulatory requirements.

 

Trionara Certificates

Trionara products are in compliance with Directive 93/42/EEC regarding medical devices (MDD) and ISO 13485 issued by KIWA MEYER Notified Body.

Trionara products are in compliance with the recommendations of ISO 13485, specifically in quality planning, target designation and continuous improvement to improve our products, services and processes.