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Code of Federal Regulations (Last Updated: November 8, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter H - Medical Devices |
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Part 830 - Unique Device Identification |
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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. |