
Diligence Makes
All the Difference
Medical technology is one of the most demanding technology markets – characterized by high requirements in terms of quality, safety, and documentation. As an experienced development partner for medical technology, we accompany our customers from the initial idea to approval for medical devices, and handle the development and production of mechatronic systems and assemblies.
Our system development in medical technology combines technological precision with regulatory expertise. We develop solutions that can be documented in accordance with standards, manufactured in a reproducible manner, and implemented economically. Through our experience in series production, we create products that function safely, can be manufactured efficiently, and meet the requirements of a highly regulated market.
Integral Component: Regulatory Compliance in Accordance with ISO 13485
Regulatory compliance is an integral part of any medical technology project. Our quality management system in accordance with ISO 13485 forms the basis for the development and production of medical devices that meet the highest requirements in terms of functional safety, traceability, and standard-compliant documentation.
We ensure that all processes from system development to series production comply with the applicable standards and regulations. Through structured processes, traceable tests, and complete documentation, we create the basis for efficient approval for medical devices and long-term product safety.
Our Technology in Use
Customer References
Feel Free to Contact Us
JÜKE Systemtechnik GmbH
Trumpenstiege 2
48341 Altenberge
Tel: +49 2505 87-0
Fax: +49 2505 87-800
Email: info@jueke.de




