On May 4, 2015, FDA launched a publicly available Global Unique Device Identification Database. This new search function can be found HERE. This website allows any person to search or download information that device labelers have submitted to the GUDID about their medical devices. The public GUDID search function is still a beta version. FDA…Read more
UDI – What can you do today to get prepared?
With the UDI final rule passed and implemented, many companies are still unfamiliar with the UDI requirements. This is a difficult and arduous process that takes a dedicated team and lots of planning. However, compliance can be achieved by starting off on the right foot. Here is a short list of how to get started.…Read more
Unique Device Identifier (UDI)
ProMedic is excited to advise you about an expansion of services related UDI compliance consulting. What is UDI? As you may know by now, FDA has instituted a new labeling requirement called Unique Device Identifier (UDI). UDI is a sophisticated bar code that will help with medical device recalls, adverse event reporting, tracking, and tracing…Read more