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Regulations last checked for updates: May 14, 2025

Title 21 - Food and Drugs last revised: May 12, 2025
All TitlesTitle 21Chapter IPart 830Subpart E - Subpart E—Global Unique Device Identification Database
  • § 830.300 - Devices subject to device identification data submission requirements.
  • § 830.310 - Information required for unique device identification.
  • § 830.320 - Submission of unique device identification information.
  • § 830.330 - Times for submission of unique device identification information.
  • § 830.340 - Voluntary submission of ancillary device identification information.
  • § 830.350 - Correction of information submitted to the Global Unique Device Identification Database.
  • § 830.360 - Records to be maintained by the labeler.
authority: 21 U.S.C. 321,331,352,353,360,360d,360i,360j,371
source: 78 FR 58823, Sept. 24, 2013, unless otherwise noted.
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