{"database": "lobbying", "table": "lobbying_activities", "rows": [[1368735, "5b35fa5a-06c8-4c7b-81e2-3bc8403f4a0e", "Q1", "ASSN OF MEDICAL DEVICE REPROCESSORS", 291732, "ASSN OF MEDICAL DEVICE REPROCESSORS", 2013, "first_quarter", "MED", "Educated Congressional staff, members of Congress, and other agency officials on the FDA-regulated, third-party reprocessing industry and ongoing efforts to implement similar regulations internationally.  Contacted VA about regulations for reprocessed single-use medical devices.", "HOUSE OF REPRESENTATIVES,SENATE,Veterans Affairs, Dept of (VA)", 0, 0, "2013-04-03T12:53:26.947000-04:00"]], "columns": ["id", "filing_uuid", "filing_type", "registrant_name", "registrant_id", "client_name", "filing_year", "filing_period", "issue_code", "specific_issues", "government_entities", "is_no_activity", "is_termination", "received_date"], "primary_keys": ["id"], "primary_key_values": ["1368735"], "units": {}, "query_ms": 33.67926302598789, "source": "Federal Register API & Regulations.gov API", "source_url": "https://www.federalregister.gov/developers/api/v1", "license": "Public Domain (U.S. Government data)", "license_url": "https://www.regulations.gov/faq"}