{
  "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": "2026-08-03",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
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  },
  "results": [
    {
      "third_party_flag": "N",
      "life_sustain_support_flag": "Y",
      "gmp_exempt_flag": "N",
      "summary_malfunction_reporting": "Ineligible",
      "product_code": "NQR",
      "openfda": {
        "pma_number": [
          "P080013",
          "P240027",
          "P040034",
          "P130014",
          "P220014"
        ],
        "registration_number": [
          "8010177",
          "3003418325",
          "3043624366",
          "3005920920",
          "3012102437",
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          "3010291427",
          "3035387162",
          "3013820501",
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      },
      "review_panel": "NE",
      "medical_specialty": "",
      "device_name": "Sealant, Dural",
      "review_code": "",
      "unclassified_reason": "",
      "medical_specialty_description": "Unknown",
      "device_class": "3",
      "definition": "Dural sealants are devices intended to aid in preventing cerebrospinal fluid leakage through suture-approximated dural wound edges.  The sealant is sprayed or layered onto sutured dural wound edges and allowed to polymerize in place.",
      "regulation_number": "",
      "implant_flag": "Y",
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}