{
  "@type": "dcat:Dataset",
  "accessLevel": "public",
  "bureauCode": [
    "009:10"
  ],
  "contactPoint": {
    "@type": "vcard:Contact",
    "fn": "openFDA",
    "hasEmail": "mailto:open@fda.hhs.gov"
  },
  "describedBy": "http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/Overview/ClassifyYourDevice/ucm2005371.htm",
  "description": "This database contains medical device names and associated information developed by the Center. It includes a three letter device product code and a Device Class that refers to the level of CDRH regulation of a given device.",
  "distribution": [
    {
      "@type": "dcat:Distribution",
      "downloadURL": "http://www.accessdata.fda.gov/premarket/ftparea/foiclass.zip",
      "mediaType": "application/zip"
    }
  ],
  "identifier": "3286eac6-86ad-4236-9281-8d09ad04e816",
  "issued": "2021-02-25",
  "keyword": [
    "cdrh"
  ],
  "landingPage": "http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPCD/PCDSimpleSearch.cfm",
  "license": "http://opendefinition.org/licenses/odc-odbl/",
  "modified": "2025-07-16",
  "programCode": [
    "009:005"
  ],
  "publisher": {
    "@type": "org:Organization",
    "name": "U.S. Food and Drug Administration"
  },
  "references": [
    "http://www.fda.gov/MedicalDevices/DeviceRegulationandGuidance/Overview/ClassifyYourDevice/ucm051668.htm"
  ],
  "theme": [
    "FDA"
  ],
  "title": "Product Classification"
}