Seemann Technologies successfully certified for MDR 2017/745

The MDR directive (Medical Device Regulation) is one of the most important certifications in medical technology. It places high demands on companies, such as:

• Extended areas of application 
• Valid and comprehensive clinical evaluations 
• Stricter requirements for technical documentation and QM 
• Introduction of a system for clear product labelling 
• and other requirements 

This extensive set of conditions has made this EU regulation a real challenge for medical technology companies. 

As a leading manufacturer of high-performance, high-quality disposable HF instruments, we are aware of our responsibility: ‘The quality of our products in use in hospitals, medical and surgical centres around the world, and therefore the safety of patients, is our top priority at Seemann Technologies - we make no compromises here,’ emphasises Managing Director Thomas Seemann. 

This is exactly what the successful MDR certification proves. We are pleased to inform our worldwide partners and customers that SEEMANN Technologies' disposable HF forceps, disposable electrodes and disposable cables are now officially MDR-certified. 

Do you have questions about our certification or SEEMANN products and would like a personal consultation? Then please contact us directly by phone or e-mail via our contact area.

Your team from SEEMANN TECHNOLOGIES