{"database": "lobbying", "table": "lobbying_activities", "rows": [[1264723, "3ef1da76-822d-4fdb-a7b9-d93f59bc382d", "Q2", "ASSN OF MEDICAL DEVICE REPROCESSORS", 291732, "ASSN OF MEDICAL DEVICE REPROCESSORS", 2012, "second_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. Initiated discussions on MDUFA reauthorization. Contacted VA about hospital regulations for reprocessed single-use medical devices.", "Commerce, Dept of (DOC),Environmental Protection Agency (EPA),Food & Drug Administration (FDA),HOUSE OF REPRESENTATIVES,SENATE,U.S. International Trade Commission (ITC),Veterans Affairs, Dept of (VA)", null, 20000, 0, 0, "2012-07-16T16:31:44.797000-04:00"]], "columns": ["id", "filing_uuid", "filing_type", "registrant_name", "registrant_id", "client_name", "filing_year", "filing_period", "issue_code", "specific_issues", "government_entities", "income_amount", "expense_amount", "is_no_activity", "is_termination", "received_date"], "primary_keys": ["id"], "primary_key_values": ["1264723"], "units": {}, "query_ms": 23.453217989299446, "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"}