We are excellent and certified!
As a manufacturer of medical devices, we have to comply with legal and regulatory requirements – so of course we are always up to date with our certifications! Secure – Simple – Reliable – DEHAS
EN DIN ISO 13485:2016
ISO certification is the basis for being allowed to manufacture medical devices.
MDSAP is an association of currently 5 countries – (USA,CAN,BRA,KOR,JPN), which mutually recognise their auditing.
Company's own testing service for the manufacture of pressure vessels
In order to be able to manufacture and test our EasyMate products (pressure vessels), we require, in addition to the type tests, the approval for the company’s own testing service (CTC).
Discover our product range!
In our product range you will only find products and articles that are designed, manufactured, tested and marketed in accordance with current standards and technical regulations, norms and legal requirements. Secure – Simple – Reliable – DEHAS