From 17 to 20 November 2025, D.med Technologies will be present at COMPAMED 2025 in Düsseldorf, Germany. As the world’s leading trade fair for suppliers and manufacturers in medical technology, COMPAMED brings together thousands of industry experts, innovators, and decision-makers to explore the latest trends and future developments in MedTech.
Innovation Meets Experience
D.med Technologies is part of the D.med Healthcare Group, headquartered in Düsseldorf, Germany, known globally for its strong track record in dialysis and extracorporeal treatments. With over 15 years of experience, we provide end-to-end support to medical device manufacturers, combining engineering excellence, regulatory expertise, and agile execution.
What You Will Find at Our Booth
At Hall 8a, Stand N11, our team will present how we support partners throughout the entire product lifecycle, with a focus in key areas such as:
- Medical Software – Cloud and embedded applications for medical devices, secure, compliant, and user-friendly.
- Cybersecurity – End-to-end protection with risk management, testing, and regulatory compliance.
- Testing & Prototyping – Design, prototyping, and testing of electronics, including PCBs and hardware.
- Regulatory Affairs & QM – Support with MDR, FDA, and ISO 13485 compliance worldwide.
- Clinical Affairs – Clinical trials, evaluations, and usability studies backed by in-house labs.
- Device Optimization – Design-to-cost, feasibility, and lifecycle optimization for medical devices.
- Test Equipment for Production – Reliable test systems to verify critical parameters such as pressure, flow, and electrical safety.
Visitors will also have the chance to learn more about our successful collaborations with some of the world’s most innovative MedTech start-ups as well as leading device manufacturers.
Why Visit Us at COMPAMED
COMPAMED is not just about showcasing products—it’s about building partnerships. At D.med Technologies, we believe collaboration is key to driving innovation in healthcare. Whether you are looking for a partner to accelerate development, strengthen compliance, or optimize your route to market, our team will be there to listen, discuss, and explore opportunities together. We will also introduce our latest developments and products in connectivity, security, and other key areas for medical devices.
👉 Join us at COMPAMED 2025 – Hall 8a / N11 – and discover how D.med Technologies can help transform your vision into reality.
Antonios is a Senior Quality & Regulatory Affairs Manager, an accomplished expert in quality management and regulatory compliance regarding development and production of medical devices with over 20 years of experience supporting startups, SMEs and multinational manufacturers.
Antonios specializes in ISO 13485, MDR, and FDA regulations, guiding organizations in the development and implementation of robust quality management systems. Acknowledging Regulatory requirements in a fast paced global environment. His hands-on approach and in-depth knowledge of technical documentation, risk management, software lifecycle management, usability engineering and clinical evaluation ensure that innovations are brought to market efficiently and in full compliance with global standards.
Dedicated to delivering sustainable outcomes, he works closely with partners to enable secure international market access with confidence.