{
  "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": "2026-06-02",
    "results": {
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  "results": [
    {
      "spl_product_data_elements": [
        "Pall Sterile Cord Blood Collection Unit Sterile Cord Blood Collection Unit WATER PHOSPHORIC ACID SODIUM CITRATE ANHYDROUS CITRIC ACID CITRIC ACID MONOHYDRATE ANHYDROUS CITRIC ACID SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE PHOSPHATE ION DEXTROSE MONOHYDRATE ANHYDROUS DEXTROSE"
      ],
      "warnings_and_cautions": [
        "WARNINGS Making multiple punctures of the umbilical cord to increase collection volume may increase the risk of contamination. Do not irradiate collected cord blood or components."
      ],
      "how_supplied": [
        "HOW SUPPLIED The Collection Unit inside the overwrap pouch, within the foil envelope, are sterile and acceptable for use in a sterile field if pouch is unopened and undamaged."
      ],
      "description": [
        "ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE SOLUTION (CPD) Sterile, non-pyrogenic fluid path. Sterilized by steam. This product is free of natural rubber latex."
      ],
      "indications_and_usage": [
        "Indications and Usage Section For collection of up to 210 ml of umbilical cord blood. Use aseptic technique. Contents inside overwrap pouch, within the foil envelope, are sterile and acceptable for use in a sterile field if pouch is unopened and undamaged; visual inspection to confirm the integrity of overwrap pouch should be performed."
      ],
      "precautions": [
        "GENERAL PRECAUTIONS Do not use if the package is damaged or seal is incomplete. Use only if solution is clear. Sealing should be done in a manner that avoids fluid splatter. Always dispose of blood-contaminated products in a manner consistent with established BIOHAZARD safety procedures."
      ],
      "information_for_patients": [
        "INFORMATION FOR PATIENTS For customer service, call: 1.800.645.6578 DonorCare is a registered trademark of ITL Corporation, Canberra, Australia. Produced under license from ThermoGenesis Corp Ensure DonorCare® Needle Guard (DCNG) is positioned on the tubing between the needle hub and Pinch Clamp. Engage Pinch Clamp. Ensure tethered cap is placed securely on the air vent. Using aseptic technique, insert needle into umbilical vein, disengage Pinch Clamp to collect cord blood, mixing frequently, according to standard procedures. Upon completion of collection, engage Pinch Clamp then withdraw needle from umbilical vein. Slide the DCNG midway over the needle hub. While holding the sides of DCNG near front, grasp tubing and pull smoothly, pulling needle into the DCNG until it locks into place. Confirm that needle is locked by listening for the second click as the needle is drawn into the DCNG. Ensure that tubing cannot be pulled through DCNG. Place the bag on a work surface. While holding the tubing above the bag, open the tethered cap on the air vent. Allow the blood to drain from the tubing into the bag. When the tubing has been drained, hold tubing vertical and seal tubing directly below the Y-piece with air vent. Detach and discard needle, DCNG, Pinch Clamp, Air Vent and tubing according to standard procedures. Determine amount of anticoagulated blood collected. If required, add sedimenting agent to CPD anticoagulated blood through Sample Port using a syringe according to standard procedures. Mix well. Take care to strip and mix any blood in tubing. Load bag into centrifuge cup. It is suggested that a means of support is used to prevent bag from collapsing and to reduce wrinkles. Centrifuge according to standard procedures to obtain mononuclear cell-rich plasma."
      ],
      "package_label_principal_display_panel": [
        "Bag label Envelope label Case Label IFU IFU"
      ],
      "set_id": "aa9340b7-cc63-e17d-e053-2a95a90ad4d9",
      "id": "46366161-f003-2826-e063-6394a90a91a5",
      "effective_time": "20251218",
      "version": "7",
      "openfda": {
        "application_number": [
          "BN800222"
        ],
        "brand_name": [
          "Pall Sterile Cord Blood Collection Unit"
        ],
        "generic_name": [
          "STERILE CORD BLOOD COLLECTION UNIT"
        ],
        "manufacturer_name": [
          "Global Life Sciences Solutions USA LLC"
        ],
        "product_ndc": [
          "79403-791"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAVENOUS"
        ],
        "substance_name": [
          "CITRIC ACID MONOHYDRATE",
          "DEXTROSE MONOHYDRATE",
          "SODIUM CITRATE",
          "SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE"
        ],
        "spl_id": [
          "46366161-f003-2826-e063-6394a90a91a5"
        ],
        "spl_set_id": [
          "aa9340b7-cc63-e17d-e053-2a95a90ad4d9"
        ],
        "package_ndc": [
          "79403-791-08"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "2968PHW8QP",
          "LX22YL083G",
          "1Q73Q2JULR",
          "593YOG76RN"
        ]
      }
    }
  ]
}