{
  "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": "2026-09-02",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 298
    }
  },
  "results": [
    {
      "has_donation_id_number": "false",
      "mri_safety": "Labeling does not contain MRI Safety Information",
      "record_status": "Published",
      "is_labeled_as_nrl": "false",
      "is_rx": "true",
      "commercial_distribution_status": "In Commercial Distribution",
      "device_description": "1 ML 30GX1/2\"",
      "public_device_record_key": "c0f4d257-909d-4352-896b-dd612e158b74",
      "has_serial_number": "false",
      "public_version_date": "2020-01-20",
      "sterilization": {
        "is_sterile": "true",
        "is_sterilization_prior_use": "false"
      },
      "is_direct_marking_exempt": "false",
      "public_version_number": "2",
      "labeler_duns_number": "054180248",
      "is_labeled_as_no_nrl": "false",
      "identifiers": [
        {
          "id": "B7442259423",
          "type": "Package",
          "issuing_agency": "HIBCC",
          "unit_of_use_id": "B7442259422",
          "quantity_per_package": "6",
          "package_status": "In Commercial Distribution",
          "package_type": "Carton"
        },
        {
          "id": "B7442259422",
          "type": "Package",
          "issuing_agency": "HIBCC",
          "unit_of_use_id": "B7442259421",
          "quantity_per_package": "5",
          "package_status": "In Commercial Distribution",
          "package_type": "Inner Case"
        },
        {
          "id": "B7442259421",
          "type": "Primary",
          "issuing_agency": "HIBCC"
        },
        {
          "id": "B7442259420",
          "type": "Unit of Use",
          "issuing_agency": "HIBCC"
        }
      ],
      "is_single_use": "true",
      "is_otc": "false",
      "version_or_model_number": "225942",
      "has_manufacturing_date": "true",
      "brand_name": "UltraFlo Insulin Syringe",
      "is_combination_product": "false",
      "is_kit": "false",
      "product_codes": [
        {
          "code": "FMF",
          "name": "Syringe, Piston",
          "openfda": {
            "device_name": "Syringe, Piston",
            "medical_specialty_description": "General Hospital",
            "regulation_number": "880.5860",
            "device_class": "2"
          }
        }
      ],
      "device_count_in_base_package": "100",
      "is_pm_exempt": "false",
      "has_lot_or_batch_number": "true",
      "company_name": "QUALITY MEDICAL PRODUCTS USA, INC.",
      "public_version_status": "Update",
      "has_expiration_date": "true",
      "is_hct_p": "false",
      "gmdn_terms": [
        {
          "code": "38501",
          "name": "Insulin syringe/needle, basic",
          "definition": "A sterile device consisting of a calibrated barrel (cylinder) with plunger intended to be used to administer an injection of insulin to a patient subcutaneously; a non-retractable needle is included, either attached or detached (usually capped for user protection). The syringe is typically made of plastic and silicone materials and will have plunger anti-sticking properties allowing smooth plunger movement. It can be used by healthcare personnel or patient, and will allow for the aspiration of the pharmaceutical from its container for direct administration to the patient or via an intravenous (IV) port, heparin lock, or saline lock. This is a single-use device.",
          "implantable": "false",
          "code_status": "Active"
        }
      ],
      "publish_date": "2019-06-24"
    }
  ]
}