Compremium Quantis CVP

Precision without Penetration

Why it exists

The Compremium Quantis CVP was created to close a long-standing gap in venous pressure assessment, preserving physiological relevance while removing the barriers that historically limited access to this insight.

It reflects Compremium’s commitment to advancing quantitative, non-invasive physiological assessment in a responsible and clinically grounded way.

Compremium Quantis CVP

What it is

The Compremium Quantis CVP is a non-invasive solution designed to enable quantified venous pressure assessment (QVPA) using ultrasound-guided measurement principles.

By combining peripheral vein visualisation with controlled external pressure, the Compremium Quantis CVP enables objective assessment of venous collapse pressure, providing a quantitative surrogate for central venous pressure without catheter insertion.

What defines it

The Compremium Quantis CVP is built around three core principles:
1. Physiological relevance
Designed to reflect venous pressure meaningfully, not indirectly.
2. Non-invasive by design
Eliminates the need for central venous access while maintaining clinical utility.
3. Quantitative and reproducible
Focused on objective measurement that can be tracked over time and across settings.
What defines it
How it fits into care

How it fits into care

The Compremium Quantis CVP is designed to support clinical decision-making, not replace it.

It provides objective context to help clinicians:

  • assess venous pressure and congestion earlier
  • understand when escalation is warranted
  • integrate venous physiology into broader patient assessment

The Breakthrough

The Compremium Quantis CVP has received FDA Breakthrough Device Designation and has been accepted into the FDA Total Product Life Cycle Advisory Program (TAP).
These programmes are designed to support earlier, more frequent, and more strategic engagement with the FDA to help expedite patient access to important device innovations.