Neoss® maintains strict quality standards regarding the safety and supply of its products.
The quality and safety processes and procedures are broad in scope and apply stringent quality and safety standards – from the quality of incoming materials through the design, development, manufacture, storage, handling and distribution of our products.
Neoss meets and are certified to the requirements from applicable medical device regulations. Our notified body conducts regular inspections of our Quality Management System to ensure continuous compliance.
→ Quality Management System certificate for ISO 13485 (MD 75473)
→ EU Quality Management System certificate, MDR (MDR 741100)
→ EU Quality Management System certificate, MDD (CE 722819)