{"data":{"id":"us/21-cfr-830.120","jurisdiction":"us","citation":"21 CFR 830.120","heading":"Responsibilities of an FDA-accredited issuing agency.","body":"To maintain its accreditation, an issuing agency must:\n(a) Operate a system for assignment of unique device identifiers (UDIs) that meets the requirements of § 830.20;\n(b) Make available information concerning its system for the assignment of UDIs;\n(c) Maintain a list of labelers that use its system for the assignment of UDIs and provide FDA a copy of such list in electronic form by December 31 of each year;\n(d) Upon request, provide FDA with information concerning a labeler that is employing the issuing agency's system for assignment of UDIs; and\n(e) Remain in compliance with the eligibility and accreditation criteria set forth in § 830.100.","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 C—FDA Accreditation of an Issuing Agency"],"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":"111f731aaa07d919adadc77131085631408344830103559b089b577848c3847e","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-830.110","next":"us/21-cfr-830.130"},"notice":"GroundRules: Original legal text. Not legal advice."}