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Sterile devices - DevelopmentAll Fresenius Kabi Product Partnering developing and manufacturing units for sterile medical devices are certified according to DIN EN ISO 13485. Our most modern 3D-CAD-Systems allow us to exchange data with our internal mould-making centre as well as with our clients.
Our engineers, technical designers / drafters and mould makers are a strong team that guarantees rapid completion of development tasks on medical devices.

Fresenius Kabi Product Partnering Medical Devices service spans the entire process chain from the customer requirement or idea to the ready-to-use final mass product. This makes it possible to support new developments and product modifications as well as product transfers of already existing product lines. Our rapid prototyping extends from the production testing tools to the stereolithography samples in co-operation with our customers. Furthermore, we are supported in our development/realization of new assembly strategies by experienced development partners in the field of special machinery.

Process Implementation

Sterile devices - Development - Process ImplementationBefore we begin to run new processes or manufacture a new product, we do a feasibility study, in which we survey everything relevant to the process, so that technical issues, support services required, manufacturing site competencies, and risk analyses are properly assessed in advance. With the results of the feasibility evaluation, we make a proposal to our partner. If this meets with agreement, we proceed to a detailed project plan and appoint a project team who will see the project through from beginning to end according to the agreed timelines.