At MEDGAS-Technik, we are committed to advancing healthcare through high-quality, reliable, and compliant medical solutions. With a strong foundation in regulatory knowledge and healthcare standards, we develop solutions that meet both clinical needs and legal requirements.

Our quality management system provides the structure and discipline behind our operations. Regulatory compliance is managed with care and precision and from manufacturing and installation through post-market oversight, we ensure that everything is safe, effective, and ready for the demands of the market.

Certified to the Highest Standards

Our solutions are engineered to align with the highest industry standards, including:

• EU MDR 2017/745 (Medical Device Regulation)
• EU MDD 93/42/EEC (Medical Device Directive)
• ISO 13485 (Quality Management Systems for Medical Devices)
• ISO 7396 (Medical Gas Pipeline Systems)

This rigorous compliance applies across our full range of offerings - from medical gas systems to pendants, bed head units, and SOT products. Each solution is designed to provide outstanding safety, performance, and reliability - giving our clients complete confidence in the systems they depend on every day.

By adhering to these standards, our products help healthcare providers reduce operational risks and long-term costs, while supporting high-quality patient care with advanced, compliant technology.

Setting the Benchmark for Quality

MEDGAS-Technik proudly maintains ISO certification across all our manufacturing, service, and installation operations. Our facilities are audited to ensure full compliance with quality management systems, reinforcing our position as an industry leader.

Our products bear the CE mark in accordance with the European Medical Device Regulation (MDR), a testament to our uncompromising approach to quality and safety. Achieving and maintaining these certifications is only possible through the dedication and expertise of our team—professionals who embody our commitment to excellence every day.