SPIE.Photonics West 2023German Exhibitors Jüke Systemtechnik GmbH

Jüke Systemtechnik GmbH

Booth number: 4105-43

About us

Jüke is an experienced service provider for product development, contract manufacturing and regulatory affairs. We work for companies in the fields of medical technology, analytical, bio and laboratory technology as well as photonics. Our experts have many years of experience with complex mechatronic assemblies and devices, firmware and software programming, system integration and documentation according to current standards and guidelines. Jüke is ISO 13485 certified and is a reliable partner for all phases of the product life cycle.


Jüke Systemtechnik GmbH
Trumpenstiege 2
48341 Altenberge

E-mail: info@jueke.de
Phone: +49 2505 87-0
Internet: www.jueke.de

Contact person:

Martin Hovestadt
E-mail: m.hovestadt@jueke.de
Phone: +49 2505 87732

Dr. Clemens Schriever
Electronics Design
E-mail: c.schriever@jueke.de
Phone: +49 2505 87754

Steffen Hovestadt
Sales Engineer
E-mail: s.hovestadt@jueke.de
Phone: +49 2505 87760

Products & Services

Jüke works exclusively for companies in the fields of medical technology, analysis, biotechnology, laboratory technology and photonics. We offer services for product development, contract manufacturing and regulatory affairs. Our main areas of activities are:

Cell analysis

Product Development

System Development / System Integration:
We turn ideas into technical solutions and reliable products.
- Requirements management according to current standards and guidelines
- Concept development and feasibility studies
- Mechanical construction and electronics design
- Firmware and software programming
- Development of prototypes, assemblies, devices and systems according to the V-model
- Obsolescence management
- Lifecycle management, product maintenance with update and upgrade
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System Development, Product Development, Engineering

Contract Manufacturing

Contract Manufacturing / Production:
Flexible production and contract manufacturing directed to the needs and requirements of our customers:
Manufacturing with state-of-the-art infrastructure with CNC machining centers and laser welding,
Assembly, partly in low-dust and air-conditioned assembly facilities,
Quality control, tests and inspections,
Prototyping, small series and serial production,
Customer-specific logistics.
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Contract Manufacturing, Production

Regulatory Affairs

Benefit from experience: We accompany the process from a validated prototype to an approved medical device.
- Consulting, concept development and implementation
- Quality and risk management
- Documentation according to CE and FDA standards and guidelines
- CE conformity assessment
- Approval support according to MDD, MDR and CFR 820
- Design transfer and product launch
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Quality Management, Regulatory Affairs, ISO 13485

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