The FDA’s Unique Device Identification (UDI) Initiative:  How Will It Affect Hospitals?

The U.S. Food and Drug Administration (FDA) is getting closer to publishing proposed regulations for unique device identifiers (UDI). Already used by some manufacturers, a UDI is much like a barcode, placed on a medical device to help track it through the entire healthcare system. The new FDA UDI rule would require the identifier be placed on all devices, and the FDA is expected to publish a draft regulation this fall with guidance on implementing the identifiers. 

This webinar, featuring an industry expert and an FDA representative, helps you learn about the current status of the rule, understand UDI and its impact on hospitals, and prepare for implementation at your facility.

Don’t miss out on this exciting educational opportunity to learn more about how to prepare for the final rule on UDIs for medical devices.

  WHO SHOULD PURCHASE
  The webinar is designed for clinical technology managers, clinical and biomedical engineers, hospital IT staff, device risk managers, field support personnel, and healthcare provider organizations.
  QUESTIONS?
 

For questions about ordering the CD, please contact AAMI publications at 1-877-249-8226 or 240-646-7031.
   

SPEAKERS

WEBINAR CD

Includes pdf of handout materials and webinar recording on CD.

WAYS TO PURCHASE

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