{
  "format": "devicerts.device.v1",
  "cite_as": "ROTEM® delta System (US/CA), Tem Innovations GmbH. deviCERTS medical device catalogue. https://devicerts.com/devices/rotem-r-201001 (data as of 2026-11-14).",
  "source": {
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    "json_url": "https://devicerts.com/devices/rotem-r-201001.json",
    "markdown_url": "https://devicerts.com/devices/rotem-r-201001.md",
    "publisher": "deviCERTS (devicerts.com)",
    "data_sources": [
      {
        "registry": "FDA GUDID (AccessGUDID)",
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      {
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        "url": "https://open.fda.gov/apis/device/recall/"
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    "registry_records_last_synced": "2026-10-23",
    "status_as_of": "2026-11-14",
    "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/rotem-r-201001",
    "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": "ROTEM® delta System (US/CA)",
    "registry_name": "ROTEM® delta System (US/CA)",
    "url": "https://devicerts.com/devices/rotem-r-201001",
    "manufacturer": {
      "name": "Tem Innovations GmbH",
      "url": "https://devicerts.com/manufacturers/tem-innovations-gmbh",
      "country": null,
      "country_basis": null,
      "fda_registration_country": "Germany"
    },
    "status": {
      "state": "active",
      "label": "Active",
      "detail": "United States"
    },
    "classification": [
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      }
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      {
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        "label": "510(k) Number",
        "values": [
          {
            "value": "K083842",
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    ],
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      "GGN",
      "JPA"
    ],
    "emdn": [],
    "gmdn": [
      {
        "code": "56690",
        "term": "Coagulation analyser IVD, laboratory, semi-automated"
      }
    ],
    "description": null,
    "noindex": true
  },
  "authorizations": [
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      "region": "United States",
      "type": "GUDID listing",
      "number": "04260160470587",
      "number_label": "UDI-DI",
      "device_udi_di": null,
      "date": "2018-03-15",
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    {
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      "date": "2010-03-23",
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      "reason": "Customer complaints about failed target ranges for alpha angle. Firm has not completed the CAPA identifying the root cause. Projected completion of the CAPA by the firm is July 2016.",
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    },
    {
      "number": "Z-1379-2015",
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      "reason": "Some of vials were found to be partially filled.",
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      "via": "K083842"
    }
  ],
  "eu_market_availability": null,
  "properties": [
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            }
          ]
        },
        {
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        {
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          ]
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      "group": "Classification",
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