{"data":{"id":"us/21-cfr-830.60","jurisdiction":"us","citation":"21 CFR 830.60","heading":"Relabeling of a device that is required to bear a unique device identifier.","body":"If you relabel a device that is required to bear a unique device identifier (UDI), you must:\n(a) Assign a new device identifier to the device, and\n(b) Keep a record showing the relationship of the prior device identifier to your new device identifier.","path":["Title 21—Food and Drugs","CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER H—MEDICAL DEVICES","PART 830—UNIQUE DEVICE IDENTIFICATION","Subpart B—Requirements for a Unique Device Identifier"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-21.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:24:47Z","sha256":"76715398aaa9c94d68ddaa7686add89fe5739bb986abfb259b9c75b9ee9ce830","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-830.50","next":"us/21-cfr-830.100"},"notice":"GroundRules: Original legal text. Not legal advice."}