Medical device manufacturers require effective vision solutions to reduce costly product recalls. Mechatronic Solutions provides industry-leading machine vision solutions to automate product inspection, verification and traceability processes while ensuring medical device safety and compliance.
Marking and registering medical devices correctly expedites the identification of defective, recalled, or expired products. It also aids in addressing issues such as counterfeiting and instills greater confidence in doctors and patients regarding the quality of used products. Medical device manufacturers who violate these regulations will be prohibited from importing, exporting, and selling their products.
The Food and Drug Administration (FDA) Unique Device Identifier (UDI) mandate and the European Commission Medical Device and In Vitro Diagnostic Regulations (MDR/IVDR) require the use of UDI systems to trace medical devices through the supply chain. The objective of the UDI initiative is to lay the groundwork for the safe and secure global distribution of all classes of medical devices.
Vision Inspection project evaluation
Our team will estimate the feasibility and costs associated with implementing an automated solution to solve your inspection problems.