The constant pursuit of an ever higher quality level of our Devices is the main criterion that we apply for the design, manufacture and marketing of our Devices.
To this end, we have implemented a quality management and control system (compliant with UNI EN ISO 9001 and UNI EN ISO 13485) which constantly monitors the physical, chemical and biological characteristics of our Devices. Quality control begins with the most stringent controls on the raw materials used and continues throughout the production process up to the delivery of the product to the customer, thus ensuring an efficient and competent post-sales service. All controls are performed according to specific applicable standards.
To ensure maximum security, all our devices have complete traceability from the raw material used to end the operator who deliberated the material.
All data and information given here are indicative and non-binding. The user is required to verify the correct compatibility of the Devices with the use they intend to perform and to strictly observe the intended purpose of the Device. For more information, please contact our Quality & Regulatory Affairs Office (firstname.lastname@example.org).
The information in this section are intended exclusively for health professionals in conformity to art. 21 d. Lgs. February 24, 1997, no. 46 subsequent modifications and supplements and guidelines of Italian Ministry of Health February 17, 2010. If you wish to access information by clicking on "healthcare professional" declare and confirm under your sole responsibility to be such.