Preclinical artificial-heart research · Freiburg

Building a modular artificial heart, one validated subsystem at a time.

Kanzler Biologicals is developing a research-stage circulatory support architecture that separates systemic flow, pulmonary flow, pulsatility, sensing and transcutaneous energy transfer into testable modules.

Development status: engineering concept and preclinical test planning. Not an approved medical device.

KB / System architectureConcept revision 06
Open engineering documentation · Click to inspect
06coordinated subsystems
130 mlsystemic stroke target
40–150beats/min concept range
16.5 l/minsystem output target

One circulation.
Distinct technical jobs.

A total artificial heart must do more than move blood. It must manage two very different pressure regimes, reproduce useful pulsatility, react to changing demand and receive energy without creating unacceptable heat.

Our modular approach isolates these problems so each can be measured, challenged and improved before system integration.

Designed as a system,
tested as modules.

Read the complete technical dossier
01

Systemic circulation

Pulsatile membrane pump

A linear-drive pressure chamber designed for systemic pressure and controlled stroke delivery.

Technical details →
02

Pulmonary circulation

Microaxial flow + pulse chamber

A low-pressure baseline pump paired with an independently controlled pulsatility module.

Technical details →
03

Energy & control

Sensing, safety and TET

Redundant control logic, implantable energy storage and transcutaneous energy transfer.

Technical details →

A transparent path from concept to bench evidence.

Target values are not test results. The project separates design assumptions, simulation, component testing and integrated validation so readers can see what is proposed—and what remains unproven.

See the validation plan
  1. 01
    Define

    Requirements, interfaces, hazards and measurable acceptance criteria.

  2. 02
    Prototype

    Module-level hardware for flow, pressure, heat and control testing.

  3. 03
    Verify

    Repeatable bench protocols with documented inputs and outcomes.

  4. 04
    Integrate

    Closed-loop system evaluation only after subsystem evidence exists.

Clear about what exists today.

Updated August 2026

Documented

System architecture

Functional decomposition, interfaces, target specifications, control concept and risk-driven validation roadmap.

Next evidence

Bench prototypes

Hydraulic characterization, hemocompatibility-oriented geometry refinement, thermal testing and fault-response verification.

Not claimed

Clinical performance

No clinical efficacy, safety, regulatory approval or patient-use claim is made by this research-stage project.

Hard biomedical problems are solved together.

We welcome focused exchange with researchers and engineers working in blood-contacting materials, pump design, controls, electronics, thermal management and preclinical testing.