Federal Register Notice: FDA is requesting comments to help the agency understand how the use of a unique device identification system may improve patient safety, e.g., by reducing medical errors, facilitating device recalls, and improving medical device adverse event reporting. The agency would also like to understand the issues associated with the use of various automatic identification technologies (e.g., bar code, radiofrequency identification). Comments should be submitted by 11/9. To view this notice, click here.