A
acro14
Dear forum members,
my company is a european manufacturer of medical devices. We want to prepare for the upcoming UDI implementation in Europe. In this context I have a question regarding traceability of products after market release: when we sell products to a wholesaler or retailer, e.g. a supermarket or medical supply store, how can traceability be assured? You maybe not know the end customer who bought a product. Are stores obliged to modify their registration systems to fit the UDI scheme?
How is this issue handled in the US? I will appreciate your replies.
my company is a european manufacturer of medical devices. We want to prepare for the upcoming UDI implementation in Europe. In this context I have a question regarding traceability of products after market release: when we sell products to a wholesaler or retailer, e.g. a supermarket or medical supply store, how can traceability be assured? You maybe not know the end customer who bought a product. Are stores obliged to modify their registration systems to fit the UDI scheme?
How is this issue handled in the US? I will appreciate your replies.