Quality
Serving
Solutions
Producer and supplier
Medica Europe occupies an important place in healthcare and continuously emphasizes the crucial importance of quality in every aspect of our services. As a versatile player in healthcare, we fulfill various key roles that are important to the sector. We function as a manufacturer and supplier of medical single-use items, compiler of procedure packages and as a distribution partner, as well as an EU importer and exporter of medical single-use products, both within the borders of Europe and beyond.
This multitude of functions requires a wide range of responsibilities. Every aspect of our business operations is subject to strict European and international regulations. These legal responsibilities ensure that all Medica Europe products and services meet the highest standards of safety and quality.
Certifications
To confirm compliance with these standards, we have achieved important certifications. We are proud of the certification according to Regulation (EU) 2017/745, also known as the Medical Device Regulation (MDR), which we have acquired since 2020. This certification shows that Medica Europe complies with the most recent European Union regulations on medical devices. In addition, the company has been certified according to ISO 13485 since 2003, an internationally recognized standard that sets specific requirements for a quality management system for medical devices. This long track record highlights our commitment to quality and our responsibility to healthcare and patients worldwide.
Quality
Producer and supplier
Medica Europe occupies an important place in healthcare and continuously emphasizes the crucial importance of quality in every aspect of our services. As a versatile player in healthcare, we fulfill various key roles that are important to the sector. We function as a manufacturer and supplier of medical single-use items, compiler of procedure packages and as a distribution partner, as well as an EU importer and exporter of medical single-use products, both within the borders of Europe and beyond.
This multitude of functions requires a wide range of responsibilities. Every aspect of our business operations is subject to strict European and international regulations. These legal responsibilities ensure that all Medica Europe products and services meet the highest standards of safety and quality.
Certifications
To confirm compliance with these standards, we have achieved important certifications. We are proud of the certification according to Regulation (EU) 2017/745, also known as the Medical Device Regulation (MDR), which we have acquired since 2020. This certification shows that Medica Europe complies with the most recent European Union regulations on medical devices. In addition, the company has been certified according to ISO 13485 since 2003, an internationally recognized standard that sets specific requirements for a quality management system for medical devices. This long track record highlights our commitment to quality and our responsibility to healthcare and patients worldwide.
Mission
Medica Europe positions itself as a leading player in the medical disposables industry, focused on relieving the burden on healthcare and delivering sustainable solutions. The pay-off ‘Serving Solutions’ serves as a guideline for all communication.
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