{
  "format": "devicerts.manufacturer.v1",
  "cite_as": "Energist. deviCERTS medical device catalogue. https://devicerts.com/manufacturers/energist (data as of 2026-11-15).",
  "source": {
    "canonical_url": "https://devicerts.com/manufacturers/energist",
    "json_url": "https://devicerts.com/manufacturers/energist.json",
    "markdown_url": "https://devicerts.com/manufacturers/energist.md",
    "publisher": "deviCERTS (devicerts.com)",
    "data_sources": [
      {
        "registry": "EUDAMED",
        "url": "https://ec.europa.eu/tools/eudamed"
      },
      {
        "registry": "FDA registration and listing",
        "url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfrl/rl.cfm"
      }
    ],
    "eudamed_record_synced": "2026-11-07",
    "fda_recalls_as_of": "2026-11-01",
    "registry_facts_computed": "2026-11-15",
    "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/manufacturers/energist",
    "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."
  },
  "manufacturer": {
    "name": "Energist",
    "url": "https://devicerts.com/manufacturers/energist",
    "registered_as": null,
    "abbreviated_name": null,
    "also_registered_as": [
      "ENERGIST LIMITED"
    ],
    "country": "United Kingdom",
    "country_basis": "from SRN",
    "eudamed_status": {
      "status": "active",
      "since_year": null
    },
    "verified": false,
    "roles": [
      "Manufacturer"
    ],
    "registrations": [
      "EUDAMED",
      "FDA"
    ],
    "identifiers": [
      {
        "label": "EUDAMED SRN",
        "value": "GB-MF-000021765"
      }
    ],
    "summary": "Energist is a medical device manufacturer based in the United Kingdom, with 3 devices listed in EUDAMED (EU Class I and IIb) as of 15 Nov 2026.",
    "noindex": false
  },
  "counts": {
    "devices": 3,
    "devices_note": null,
    "certificates": 2,
    "fda_recalls_matched_by_name": 0,
    "fda_recalls_ongoing": 0,
    "fda_recalls_ongoing_recent": 0,
    "fda_recalls_ongoing_before": null,
    "fda_establishments": 1,
    "sites": 0
  },
  "registry_facts": {
    "covers": "Every device of the manufacturer. A device listed in two registries counts in both.",
    "registries": [
      {
        "registry": "EUDAMED",
        "devices": 3
      }
    ],
    "device_classes": [
      {
        "class": "EU Class I",
        "devices": 2
      },
      {
        "class": "EU Class IIb",
        "devices": 1
      }
    ],
    "top_emdn_categories": [
      {
        "code": "Z12",
        "name": "Instruments for functional explorations and therapeutic interventions",
        "url": "https://devicerts.com/categories/emdn/Z12",
        "devices": 3
      }
    ]
  },
  "related": {
    "site_of": null,
    "part_of": null,
    "sites": [],
    "authorised_representatives": [
      {
        "name": "Advena Limited",
        "url": "https://devicerts.com/representatives/advena-limited-mt-ar-000000234",
        "country": "Malta"
      }
    ]
  },
  "devices": {
    "shown": 3,
    "total": 3,
    "all_devices_url": "https://devicerts.com/manufacturers/energist",
    "items": [
      {
        "name": "NeoGen",
        "url": "https://devicerts.com/devices/neogen-930-025",
        "model_reference": "930-025",
        "device_class": "Class IIb",
        "registries": [
          "EUDAMED"
        ],
        "status": "Active",
        "decision_date": null,
        "open_recall": false
      },
      {
        "name": "NeoGen",
        "url": "https://devicerts.com/devices/neogen-930-026",
        "model_reference": "930-026",
        "device_class": "Class I",
        "registries": [
          "EUDAMED"
        ],
        "status": "Active",
        "decision_date": null,
        "open_recall": false
      },
      {
        "name": "NeoGen Footswitch",
        "url": "https://devicerts.com/devices/neogen-footswitch-230-027",
        "model_reference": "230-027",
        "device_class": "Class I",
        "registries": [
          "EUDAMED"
        ],
        "status": "Active",
        "decision_date": null,
        "open_recall": false
      }
    ]
  },
  "certificates": [
    {
      "number": "GB25/00000090",
      "type": "Quality management system",
      "legislation": "MDR",
      "notified_body": "SGS Belgium NV",
      "issued": "2026-01-20",
      "expires": "2030-05-08",
      "status": "issued",
      "no_longer_listed": false
    },
    {
      "number": "GB25/00000090",
      "type": "Quality management system",
      "legislation": "MDR",
      "notified_body": "SGS Belgium NV",
      "issued": "2025-05-08",
      "expires": "2030-03-08",
      "status": "supplemented",
      "no_longer_listed": false
    }
  ],
  "recalls": []
}