{"@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"}