Perfusion Lab
Integrated Experimental Platforms

Aeternus Perfusion Lab

Build Your Experimental Perfusion System

AEP-IPS-01

From individual components to integrated experimental fluid-circulation, monitoring and control platforms.

From individual modules to a complete experimental perfusion platform — the existing Aeternus Perfusion Lab modules presented as one configurable experimental system.

Integrated laboratory perfusion research platform combining pumps, fluid circuits, sensors, heat exchange and a control interface

Conceptual visualization — final components, sensors, interfaces and system specifications depend on the requested experimental configuration.

Choose Your Approach

Four Ways to Work With Aeternus Perfusion Lab

System Architecture

Conceptual Modular Architecture

Reservoir
Pump System
Pressure / Flow / Temperature Monitoring
Heat Exchange
Experimental Chamber
Return Circuit

Control & Data System

Bidirectional monitoring, control and data acquisition across the experimental circuit.

Final system architecture is defined according to experimental requirements.

Available Modules

The Aeternus Perfusion Lab Module Family

Build Your System

Configure Your Platform

Select a system type, application and modules, then describe your technical requirements — our engineering team evaluates the complete experimental architecture.

1. System Type
2. Application
3. Modules
4. Technical Requirements
5. Contact
6. Summary

One Platform. Multiple Configurations.

Researchers can request an individual module, combine selected technologies, or configure a complete experimental perfusion platform according to their laboratory requirements.

01

Individual Components

02

Modular Integration

03

Complete Experimental Platform

Important Information

AEP-IPS-01 is presented as a configurable laboratory and experimental engineering platform.

It is not presented for clinical use, diagnosis or treatment.

Final components, materials, sensors, pumps, interfaces, software functions and system specifications depend on the requested experimental configuration and engineering evaluation.

Compatible third-party components may be integrated where appropriate.

The platform is not described as medical grade, sterile, CE certified, RUO certified or clinically approved unless such status is specifically documented for the supplied configuration.