{
  "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": "2026-10-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 47
    }
  },
  "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": "Integra® Miltex® Mathieu Urethral and IUD Removal Forceps 11-3/4\" Shaft, Serrated Jaws 3.5mm x 19mm",
      "public_device_record_key": "a143de97-a5ce-45ca-a40a-8d5255b51dc2",
      "has_serial_number": "false",
      "public_version_date": "2023-04-28",
      "sterilization": {
        "is_sterile": "false",
        "is_sterilization_prior_use": "true",
        "sterilization_methods": "Moist Heat or Steam Sterilization"
      },
      "is_direct_marking_exempt": "false",
      "public_version_number": "6",
      "labeler_duns_number": "081277700",
      "is_labeled_as_no_nrl": "false",
      "identifiers": [
        {
          "id": "H834291020",
          "type": "Secondary",
          "issuing_agency": "HIBCC"
        },
        {
          "id": "10381780427759",
          "type": "Primary",
          "issuing_agency": "GS1"
        }
      ],
      "is_single_use": "false",
      "is_otc": "false",
      "version_or_model_number": "29-102",
      "has_manufacturing_date": "false",
      "brand_name": "Integra® Miltex®",
      "is_combination_product": "false",
      "is_kit": "false",
      "product_codes": [
        {
          "code": "HHF",
          "name": "REMOVER, INTRAUTERINE DEVICE, CONTRACEPTIVE, HOOK-TYPE",
          "openfda": {
            "device_name": "Remover, Intrauterine Device, Contraceptive, Hook-Type",
            "medical_specialty_description": "Obstetrics/Gynecology",
            "regulation_number": "884.4530",
            "device_class": "1"
          }
        }
      ],
      "device_count_in_base_package": "1",
      "is_pm_exempt": "true",
      "has_lot_or_batch_number": "true",
      "customer_contacts": [
        {
          "phone": "+1(800)654-2873",
          "email": "custsvcnj@integralife.com"
        }
      ],
      "catalog_number": "29-102",
      "company_name": "INTEGRA LIFESCIENCES PRODUCTION CORPORATION",
      "public_version_status": "Update",
      "has_expiration_date": "false",
      "is_hct_p": "false",
      "gmdn_terms": [
        {
          "code": "12032",
          "name": "Intrauterine device removal hook, reusable",
          "definition": "A hand-held manual instrument intended to be used by a physician for the extraction of an intrauterine device (IUD). The proximal end forms a handle which may vary in shape and which tapers toward the distal end to form a hook. It is typically made of high-grade stainless steel. This is a reusable device.",
          "implantable": "false",
          "code_status": "Active"
        }
      ],
      "publish_date": "2018-01-10"
    }
  ]
}