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As a manufacturer of Medical Devices, Leventon has a Quality Policy that is aimed at fully meeting the expectations of customers (distributors and, through them, hospitals centers, health personnel and patients) as regards the Quality and Service of its products, as well as all legal and regulatory requirements of the sector.

Highest quality assurance standards:
CE Mark , Leventon FDA Registered establishment since 1985, MDSAP Certification – Medical Device Single Audit Program (April 2021), ISO 13485:2016,  MDR – EU Medical Device Regulations (2021)