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  1. Regulations
    All Titles
  2. title 21
    Food and Drugs
  3. chapter I-i7
    CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)
  4. part 830
    PART 830—UNIQUE DEVICE IDENTIFICATION
  5. subpart E
    Subpart E—Global Unique Device Identification Database

Subpart 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.
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