{"data":{"id":"us/21-cfr-830.210","jurisdiction":"us","citation":"21 CFR 830.210","heading":"Eligibility for use of FDA as an issuing agency.","body":"When FDA acts as an issuing agency, any labeler will be permitted to use FDA's unique device identification system, regardless of whether the labeler is considered a small business.","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 D—FDA as 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":"92812f04456d6aa7c0d69a8ae4334490a0641f18e28e303c07096c491bac7a69","source_id":"us-cfr","stale":true,"prev":"us/21-cfr-830.200","next":"us/21-cfr-830.220"},"notice":"GroundRules: Original legal text. Not legal advice."}