Capturing Unique Device Identifier Data on Non-Sterile Orthopedic Implants

  • Magazine Article
  • TBMG-34970
Published August 01, 2019 by Tech Briefs Media Group in United States
  • English

Now that medical devices are being labeled and uniquely identified to meet the requirements of the U.S. Food and Drug Administration (FDA) Unique Device Identifier (UDI) Rule, healthcare providers have an opportunity to capture and leverage the data contained in these unique device identifiers (UDIs) to improve the quality of care.