1. Collections
  2. Code of Federal Regulations
  3. Title 21
  4. Chapter I
  5. Subchapter H

Part 830

21 C.F.R. Part 830

Unique Device Identification

AGeneral ProvisionsBRequirements for a Unique Device IdentifierCFDA Accreditation of an Issuing AgencyDFDA as an Issuing AgencyEGlobal Unique Device Identification Database
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