The legislation in the field of medical devices requires high standards for their products and services, as they contribute directly to maintaining and supporting the vital functions of the patients,
this makes us more accountable to our customers and consumers.
We have formalized and certified our procedures and production processes according to the standards ISO9001 and ISO13485. Our company's quality system applies to all the phases of organization and production.
All components sold are CE-certified and subject to quality controls, the internal.
We are qualified and registered as a manufacturer of medical devices from the database, MINISTRY of HEALTH for medical devices and relevant systems medical gas and vacuum (IDGM) and systems of evacuation of anaesthetic gases (SDEGA)
The certification of business processes and product is certified by IMQ s.p...
Certification IQNET (the International Certification Network), ensures the international trade compliance of our management system in the member countries belonging to the network.