{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-09-08",
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          "manufacturer_d_address_2": "900 RUE DU MAS DE VERCHANT",
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          "udi_di": "",
          "udi_public": "",
          "openfda": {
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            "No Code Available"
          ]
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      "manufacturer_g1_country": "",
      "manufacturer_contact_city": "",
      "mdr_report_key": "6427844",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "date_manufacturer_received": "20160225",
      "manufacturer_name": "",
      "report_source_code": "Manufacturer report",
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      "mdr_text": [
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          "mdr_text_key": "70684044",
          "text_type_code": "Additional Manufacturer Narrative",
          "patient_sequence_number": "1",
          "text": "THE DEVICE RO 14 030 HAS BEEN INSPECTED FOR INVESTIGATION PURPOSE. THE TESTS PERFORMED CONFIRMED THAT THERE WAS AN INTERACTION BETWEEN THE HIGH VOLTAGE SURGE GENERATED BY THE TORIC ISOLATION TRANSFORMER AND THE HOSPITAL ELECTRICAL SYSTEM THAT CAUSED THE ISSUE. (B)(4)."
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        }
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      "manufacturer_contact_postal_code": "",
      "manufacturer_contact_exchange": "",
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    }
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}