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  1. LII
  2. Electronic Code of Federal Regulations (e-CFR)
  3. Title 21—Food and Drugs
  4. CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  5. SUBCHAPTER H—MEDICAL DEVICES
  6. PART 830—UNIQUE DEVICE IDENTIFICATION
  7. Subpart E—Global Unique Device Identification Database

21 CFR Part 830 - Subpart E - Global Unique Device Identification Database

  • CFR
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  1. § 830.300 Devices subject to device identification data submission requirements.
  2. § 830.310 Information required for unique device identification.
  3. § 830.320 Submission of unique device identification information.
  4. § 830.330 Times for submission of unique device identification information.
  5. § 830.340 Voluntary submission of ancillary device identification information.
  6. § 830.350 Correction of information submitted to the Global Unique Device Identification Database.
  7. § 830.360 Records to be maintained by the labeler.
Source:
78 FR 58826, Sept. 24, 2013, unless otherwise noted.

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