You can benefit from our team's 30 year experience in the design and production of medical breathing solutions
Our EN ISO 13485 certified facilities and procedures ensure maximum compliance with applicable international standards and regulations.
Design
Tooling and mould making
Extrusion
Injection moulding
Medical equipment manufacturing
Quality control
Cleanroom
Sterilisation
Storage
DEAS can provide full Technical Documentation to allow you to market your OEM/OBL project in full compliance with EU Medical Device Regulation (MDR) and Medical Devices Directives (MDD)
Learn more about how DEAS can help you in your production needs