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Code of Federal Regulations (Last Updated: May 6, 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 B - Requirements for a Unique Device Identifier |
§ 830.60 - Relabeling of a device that is required to bear a unique device identifier.
Latest version.
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§ 830.60 Relabeling of a device that is required to bear a unique device identifier.
If you relabel a device that is required to bear a unique device identifier (UDI), you must:
(a) Assign a new device identifier to the device, and
(b) Keep a record showing the relationship of the prior device identifier to your new device identifier.
[78 FR 58825, Sept. 24, 2013]