{
  "format": "devicerts.device.v1",
  "cite_as": "Vt-1230-50, Summit Medical, LLC. deviCERTS medical device catalogue. https://devicerts.com/devices/na-vt-1230-50 (data as of 2026-11-15).",
  "source": {
    "canonical_url": "https://devicerts.com/devices/na-vt-1230-50",
    "json_url": "https://devicerts.com/devices/na-vt-1230-50.json",
    "markdown_url": "https://devicerts.com/devices/na-vt-1230-50.md",
    "publisher": "deviCERTS (devicerts.com)",
    "data_sources": [
      {
        "registry": "FDA GUDID (AccessGUDID)",
        "url": "https://accessgudid.nlm.nih.gov/"
      },
      {
        "registry": "FDA recalls",
        "url": "https://open.fda.gov/apis/device/recall/"
      }
    ],
    "registry_records_last_synced": "2026-10-23",
    "status_as_of": "2026-11-15",
    "license": "CC BY 4.0",
    "license_url": "https://creativecommons.org/licenses/by/4.0/",
    "license_scope": "The deviCERTS layout and text are licensed under CC BY 4.0. Registry data remain under their source terms: U.S. FDA data (openFDA, AccessGUDID) are U.S. public domain; EUDAMED data are subject to the European Commission reuse terms.",
    "attribution": "DevicErts, https://devicerts.com/devices/na-vt-1230-50",
    "disclaimer": "Compiled by deviCERTS (devicerts.com) from public medical device registries (EUDAMED, European Commission; U.S. FDA via openFDA; AccessGUDID, U.S. National Library of Medicine). deviCERTS is not an official register and gives no regulatory advice: the record in the registry itself prevails."
  },
  "device": {
    "name": "Vt-1230-50",
    "registry_name": "VT-1230-50",
    "url": "https://devicerts.com/devices/na-vt-1230-50",
    "manufacturer": {
      "name": "Summit Medical, LLC",
      "url": "https://devicerts.com/manufacturers/summit-medical-llc",
      "country": "United States",
      "country_basis": null,
      "fda_registration_country": null
    },
    "status": {
      "state": "active",
      "label": "Active",
      "detail": "United States"
    },
    "classification": [
      {
        "class": "Class II",
        "system": "US FDA"
      }
    ],
    "identifiers": [
      {
        "label": "Primary DI / UDI-DI",
        "values": [
          {
            "value": "00385640002233",
            "registries": [
              "FDA GUDID (AccessGUDID)"
            ]
          }
        ]
      },
      {
        "label": "510(k) Number",
        "values": [
          {
            "value": "K830228",
            "registries": [
              "FDA GUDID (AccessGUDID)"
            ]
          }
        ]
      }
    ],
    "product_codes": [
      "ETD"
    ],
    "emdn": [],
    "gmdn": [
      {
        "code": "33794",
        "term": "Tympanostomy tube"
      }
    ],
    "description": null,
    "noindex": true
  },
  "authorizations": [
    {
      "registry": "GUDID",
      "region": "United States",
      "type": "GUDID listing",
      "number": "00385640002233",
      "number_label": "UDI-DI",
      "device_udi_di": null,
      "date": "2016-09-16",
      "date_kind": "listed",
      "decision_code": null,
      "expires": null,
      "withdrawn": null,
      "status": "Listed",
      "status_note": "GUDID: not in commercial distribution",
      "derived_from_gudid": false
    },
    {
      "registry": "GUDID",
      "region": "United States",
      "type": "FDA 510(k)",
      "number": "K830228",
      "number_label": null,
      "device_udi_di": null,
      "date": "1983-03-07",
      "date_kind": "decision",
      "decision_code": "SESE",
      "expires": null,
      "withdrawn": null,
      "status": "Active",
      "status_note": null,
      "derived_from_gudid": true
    }
  ],
  "no_longer_listed_by": [],
  "certificates": [],
  "recalls": [
    {
      "number": "Z-1731-2014",
      "classification": "Class II",
      "status": "terminated",
      "initiated": "2014-05-12",
      "reason": "One lot of ventilation tubes have mixed tubes with wire attached to the slanted flange and ventilation tubes with wire attached to the straight flange.  This poses no health hazard to the user or patient.",
      "applies": "this device",
      "via": "K830228"
    }
  ],
  "eu_market_availability": null,
  "properties": [
    {
      "group": "Identity",
      "fields": [
        {
          "label": "Generic name",
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            {
              "value": "Tympanostomy tube",
              "registries": [
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              ]
            }
          ]
        },
        {
          "label": "Model / reference",
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            {
              "value": "VT-1230-50",
              "registries": [
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              ]
            }
          ]
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    },
    {
      "group": "Identifiers",
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          "label": "Primary DI / UDI-DI",
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            {
              "value": "00385640002233",
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              ]
            }
          ]
        },
        {
          "label": "510(k) Number",
          "values": [
            {
              "value": "K830228",
              "registries": [
                "FDA GUDID (AccessGUDID)"
              ]
            }
          ]
        },
        {
          "label": "FDA product code",
          "values": [
            {
              "value": "ETD",
              "registries": [
                "FDA GUDID (AccessGUDID)"
              ]
            }
          ]
        },
        {
          "label": "GMDN term",
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              "value": "Tympanostomy tube",
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    {
      "group": "Classification",
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        {
          "label": "Device class",
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            {
              "value": "Class II",
              "registries": [
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          ]
        },
        {
          "label": "Regulation number",
          "values": [
            {
              "value": "874.3880",
              "registries": [
                "FDA GUDID (AccessGUDID)"
              ]
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          ]
        },
        {
          "label": "GUDID distribution status",
          "values": [
            {
              "value": "Not in Commercial Distribution",
              "registries": [
                "FDA GUDID (AccessGUDID)"
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            }
          ]
        }
      ]
    },
    {
      "group": "Clinical & Handling",
      "fields": [
        {
          "label": "MRI safety",
          "values": [
            {
              "value": "MR Conditional",
              "registries": [
                "FDA GUDID (AccessGUDID)"
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            }
          ]
        }
      ]
    },
    {
      "group": "Properties",
      "fields": [
        {
          "label": "Supplied sterile",
          "values": [
            {
              "value": "Yes",
              "registries": [
                "FDA GUDID (AccessGUDID)"
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            }
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        },
        {
          "label": "Single use",
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            {
              "value": "Yes",
              "registries": [
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        },
        {
          "label": "Implantable",
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            {
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        {
          "label": "Prescription use",
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        {
          "label": "Lot / batch number",
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              "value": "Yes",
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          "label": "Expiration date",
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        },
        {
          "label": "Sterilise before use",
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              "registries": [
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          ]
        },
        {
          "label": "Contains latex",
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        {
          "label": "Over-the-counter",
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          "label": "Convenience kit",
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          "label": "Combination product",
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        },
        {
          "label": "HCT/P",
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        {
          "label": "Premarket exempt",
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        {
          "label": "Serial number",
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        },
        {
          "label": "Manufacturing date",
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}
