Premise
MC Bio S.r.l. markets medical devices that comply with Regulation (EU) 2017/745 (MDR), Directive 93/42/EEC on Medical Devices (MDD), and current national legislation. Sales are strictly reserved for individuals authorized to practice medicine, specifically surgeons and dentists.

Scope of Application
These contractual conditions govern both online and offline sales of medical devices offered by MC Bio S.r.l. to healthcare professionals.

Purchase Requirements
The buyer must demonstrate, through registration and document verification, that they are authorized to practice medicine (as a surgeon or dentist). MC Bio S.r.l. reserves the right to refuse orders from unqualified individuals.

Product Compliance
All devices sold are CE marked and comply with European and Italian regulations regarding safety, efficacy, and traceability.

Liability
MC Bio S.r.l. is not liable for the improper use of medical devices by unauthorized individuals or for uses other than those intended by the manufacturer.