{
  "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": "2026-07-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 19
    }
  },
  "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": "false",
      "commercial_distribution_status": "In Commercial Distribution",
      "device_description": "Box of 200 Sterile Single-Use Lancing Device 30Gauge",
      "public_device_record_key": "3efdd12c-01f5-4d0f-b784-090d640a1e6f",
      "has_serial_number": "false",
      "public_version_date": "2021-03-08",
      "sterilization": {
        "is_sterile": "true",
        "is_sterilization_prior_use": "false"
      },
      "is_direct_marking_exempt": "false",
      "public_version_number": "1",
      "labeler_duns_number": "718296825",
      "is_labeled_as_no_nrl": "false",
      "identifiers": [
        {
          "id": "20812608030228",
          "type": "Package",
          "issuing_agency": "GS1",
          "unit_of_use_id": "00812608030224",
          "quantity_per_package": "24",
          "package_status": "In Commercial Distribution",
          "package_type": "Cardboard box"
        },
        {
          "id": "00812608030224",
          "type": "Primary",
          "issuing_agency": "GS1"
        },
        {
          "id": "00812608030248",
          "type": "Unit of Use",
          "issuing_agency": "GS1"
        }
      ],
      "is_single_use": "true",
      "is_otc": "true",
      "version_or_model_number": "024-206",
      "has_manufacturing_date": "false",
      "brand_name": "OneTouch Delica Safety",
      "is_combination_product": "false",
      "is_kit": "false",
      "product_codes": [
        {
          "code": "FMK",
          "name": "Lancet, Blood",
          "openfda": {
            "device_name": "Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature",
            "medical_specialty_description": "General, Plastic Surgery",
            "regulation_number": "878.4850",
            "device_class": "2"
          }
        }
      ],
      "device_count_in_base_package": "200",
      "is_pm_exempt": "true",
      "has_lot_or_batch_number": "true",
      "customer_contacts": [
        {
          "phone": "1 888 567-3003",
          "email": "customerservice@lifescan.com"
        }
      ],
      "catalog_number": "OTD Safety 30g US/CA/LATAM 200",
      "company_name": "ASAHI POLYSLIDER COMPANY,LIMITED",
      "public_version_status": "New",
      "has_expiration_date": "true",
      "is_hct_p": "false",
      "gmdn_terms": [
        {
          "code": "61578",
          "name": "Manual blood lancing device, single-use",
          "definition": "A sterile, hand-held manual instrument intended to be used for controlled skin puncture/cut to obtain a capillary blood specimen, performed by a healthcare provider (e.g., on a neonate) or a patient (e.g., a diabetic), typically at the fingertip or ear lobe. It includes a preloaded lancet tip, and has a manually-powered mechanism (e.g., spring-loaded) which enables the tip to puncture to a predetermined depth and blood subsequently to be squeezed out of the puncture site. This is a single-use device.",
          "implantable": "false",
          "code_status": "Active"
        }
      ],
      "publish_date": "2021-02-26",
      "device_sizes": [
        {
          "type": "Needle Gauge",
          "value": "30",
          "unit": "Gauge"
        }
      ]
    }
  ]
}