{"data":{"id":"us/21-cfr-830.330","jurisdiction":"us","citation":"21 CFR 830.330","heading":"Times for submission of unique device identification information.","body":"(a) The labeler shall submit to FDA the information required by § 830.310 no later than the date the label of the device must bear a unique device identifier under § 801.20 of this chapter.\n(b) The labeler of a device shall submit to FDA an update to the information required by § 830.310 whenever the information changes. The updated information must be submitted no later than the date a device is first labeled with the changed information. If the information does not appear on the label of a device, the updated information must be submitted within 10 business days of the change.","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 E—Global Unique Device Identification Database"],"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":"efd2995fa5c534c4b701ed080e73d916c027dc8ecd013dc746881774c0d89e9e","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-830.320","next":"us/21-cfr-830.340"},"notice":"GroundRules: Original legal text. Not legal advice."}