“Quality eases the pain caused by the price.”

Prof. Dr. Hans-Jürgen Quadbeck-Seeger (*1939)
German chemist

The main supplier and partner of Med Baltic ADEBO Medical & Trade GmbH fulfills the requirements of DIN EN ISO 13485:2016 and can present the corresponding certificates. Testing as well as monitoring is ensured by the German testing body PFI.

The quality of our products is also checked during production by our inspectors for any defects or deviations from the quality parameters. Through the final random inspection before shipment, also known as Pre-shipment Inspection (PSI), we check our products according to the applicable EU standard for the acceptable quality parameter including AQL. In all our inspections, we rely on the internationally recognized ANSI / ASQC Z1.4 (ISO 2859-1) statistical test method. Its comprehensive criteria cover the following areas: Functionality, Performance, Durability, General Appearance and Dimensions.

All products are marked with a batch or LOT number. This allows us to easily and quickly ensure the traceability of our products.

All offered Med Baltic products already meet requirements of the new MP Regulation (EU) 2017/745 (MDR – Medical Device Regulation), which came into force on May 25, 2017.

A declaration of harmlessness for contact with foodstuffs has been issued for the gloves by DEKRA.