The Food and Drug Administration (FDA) is seeking information on how the use of a unique identifier system for medical devices may reduce medical errors, facilitate device recalls and improve medical device adverse event reporting.
A notice will appear in Friday's Federal Register (www.accessdata.fda.gov/scripts/oc/ohrms/advdisplay.cfm). The agency is seeking public comment for the next 90 days. A public meeting is planned in the fall; FDA will provide details when they become available. The comments will be used to help the agency determine what next steps the agency should take related to a unique device identifier (UDI) system for medical devices.
"Much like the bar code rule for drugs and biological products, unique identifiers for medical devices could have many potential benefits for improving the quality of care for patients," said Daniel Schultz, M.D., Director, Center for Devices and Radiological Health, FDA. "A unique device identifier system could have broad applications in reducing medical errors, facilitating device recalls, improving medical device adverse event reporting and encouraging cost effectiveness by improving delivery and supply chain efficiency."
The number and complexity of medical devices is growing. It is important for FDA to quickly identify new risks and work with industry and device users to manage these risks appropriately. A UDI system may be used to identify a device and the information associated with that device throughout its lifetime. For example, a UDI could identify which devices are compatible, such as implanted devices being used safely with magnetic resonance imaging (MRI) systems.
Over the past year, FDA met with various stakeholders and found that most supported the development of a UDI system as a way to improve patient safety. FDA also learned from the meetings that stakeholders recognize that such a system could provide supportive benefits, such as better management of the purchase, distribution and use of medical devices.