SciTransfer
Organization

RESPINOR AS

Norwegian medical device SME developing continuous ultrasound-based diaphragm monitoring for mechanically ventilated ICU patients.

Technology SMEhealthNOSMENo active H2020 projects
H2020 projects
2
As coordinator
2
Total EC funding
€3.0M
Unique partners
0
What they do

Their core work

Respinor is a Norwegian medical technology SME developing continuous diaphragm monitoring devices for patients on mechanical ventilation in intensive care units. Their core product uses ultrasound-based sensing to track diaphragm activity in real time, helping clinicians decide when a patient is ready to be weaned off a ventilator. The work sits at the intersection of critical-care medicine, medical device engineering, and non-invasive patient monitoring. In short, they build clinical hardware that aims to shorten ICU stays and reduce ventilator-induced complications.

Core expertise

What they specialise in

Diaphragm monitoring for mechanically ventilated patientsprimary
2 projects

Both H2020 projects (DiaMon Phase 1 in 2016 and DiaMon Phase 2 in 2017-2020) are dedicated to continuous diaphragm monitoring technology.

Ultrasound-based non-invasive medical sensingprimary
2 projects

The DiaMon product line applies continuous ultrasound measurement at the bedside, as described in both funded projects.

ICU clinical device development and validationprimary
1 project

The EUR 2.99M SME Phase 2 DiaMon project (2017-2020) covered full clinical development and market readiness for the ICU setting.

Medical device commercialisation (SME instrument pathway)secondary
2 projects

Progression from SME-1 feasibility (2016) to SME-2 innovation project (2017-2020) demonstrates a full commercialisation trajectory.

Evolution & trajectory

How they've shifted over time

Early focus
Diaphragm monitoring feasibility
Recent focus
ICU diaphragm monitoring device

Respinor's H2020 trajectory is narrow and deliberate: a 2016 SME Phase 1 feasibility study to validate the market and technical concept of continuous diaphragm monitoring, followed directly by a EUR 2.99M SME Phase 2 project (2017-2020) to develop, clinically test and prepare the product for market. Rather than broadening their topic, they deepened a single product line, moving from feasibility assessment to clinical-grade device development. The company is a classic single-product deep-tech SME rather than a multi-domain research group.

They are heading toward clinical deployment and commercialisation of their diaphragm monitoring device, making them relevant for partners interested in ICU validation studies, distribution, or integration with ventilator ecosystems.

Collaboration profile

How they like to work

Role: consortium_leaderReach: European

Respinor used H2020 as a single-beneficiary SME instrument pathway, coordinating both of their projects without recorded consortium partners. This pattern is typical of a product-focused medical technology SME that treats EU funding as product development capital rather than as a collaboration vehicle. Partners should expect a company that drives its own roadmap and would join a consortium as the clinical-device owner rather than as a generic research contributor.

No recorded consortium partners across their two H2020 projects, reflecting the single-beneficiary SME instrument scheme. Their footprint is Norway-centred with an implicit European market horizon through the SME-2 commercialisation project.

Why partner with them

What sets them apart

Respinor is one of very few European SMEs focused specifically on continuous, non-invasive diaphragm monitoring for ventilated ICU patients — a narrow clinical niche with direct implications for weaning protocols and ICU length of stay. They have taken a product through the full SME instrument pipeline, from feasibility to clinical development with nearly EUR 3M of EC funding. Partner with them if you need a dedicated medical device company with a validated product in critical-care respiratory monitoring, not a generalist research group.

Notable projects

Highlights from their portfolio

  • DiaMon (SME-2)
    EUR 2.99M single-beneficiary SME Phase 2 grant (2017-2020) to develop and clinically validate the continuous diaphragm monitoring device for ICU use — their flagship project.
  • DiaMon (SME-1)
    EUR 50,000 feasibility study in 2016 that directly seeded the successful Phase 2 award, showing a clean SME instrument progression.
Cross-sector capabilities
medical devicesdigital health / clinical sensingcritical care clinical research
Analysis note: Analysis based on only two H2020 projects, both for the same product (DiaMon) under the single-beneficiary SME instrument. No consortium partners or keyword tags were available, so expertise areas are inferred from project titles and funding scheme rather than from a broader project portfolio.