Leukotrap Wb System Solution
Product Images NDC 87069-136

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Leukotrap Wb System (NDC 87069-136). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gvs Tm Inc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Case Label (Case Label 1)

Label for Leukotrap WB System by GVS TM Inc, a CPDA-1 Double Blood Bag Unit with In-Line WBF Filter and Sampling System. Designed for collection of 500 ml whole blood. The label includes manufacturer address, REF 136-62, and indicates sterile, nonpyrogenic fluid path sterilized by steam. Quantity is 18 units, made in Mexico, with barcode and regulatory symbols.*

FDA Label Image

Ifu 1 (Ifu Page 1)

Diagram of the Leukotrap WB System CPDA-1 Blood Bag Unit with In-Line WBF Filter (WBF2) and Sampling System by GVS TM Inc. The illustration details components including a Collection Bag, WBF Filter, Sample Diversion Pouch, Storage Bag, Satellite Bag, donor needle, labeled tubing, and a Sample Needle Assembly with Vacuum Tube Holder and Lid. Precautions, warnings, and tubing specifications are noted around the diagram.*

FDA Label Image

Ifu 2 (Ifu Page 2)

An instructional diagram and detailed multi-step text outlining blood collection and processing using the Leukotrap WB System with a sample diversion pouch and pre-attached vacuum tube holder. The diagram depicts the donor needle, sample diversion pouch, vacuum tube holder with lid, and related components. Text includes phlebotomy steps, warnings, blood collection and discontinuation procedures, and blood filtration instructions.*

FDA Label Image

Ifu 3 (Ifu Page 3)

Instructions for the Leukotrap WB System, including filtration, centrifugation, preparing the set by automated or manual methods, expressing plasma with notes on handling, sealing and detaching tubing, storing CPDA-1 preserved red blood cells, and quality control testing requirements. The panel also explains symbols for manufacturer, sterility, lot number, and usage restrictions.*

FDA Label Image

Pouch Label (Leukotrap 19)

Label for Leukotrap WB System CPDA-1 Double Blood Bag Collection System by GVS TM Inc. The label details a 500 ml blood bag unit with CPDA-1 anticoagulant solution and in-line WBF filter and sampling system. It specifies 3 units per package, sterile, nonpyrogenic fluid path, and instructions to store at room temperature with a 30-day use period after opening.*

FDA Label Image

Bag Label 3 (Plasma 4)

Label image for Leukotrap WB System CPDA-1 Blood Bag Collection System by GVS TM Inc. The label includes instructions for placing the donation identification number and ABO label. It specifies the bag is intended for plasma and marks the product as sterile and prescription use only. Manufacturer address is 1630 W Industrial Park St, Covina, CA 91722, USA.*

FDA Label Image

Bag Label 2 (Red Blood Cells 8)

Label for Leukotrap WB System CPDA-1 Blood Bag Collection System by GVS TM Inc. The bag is intended for red blood cells storage at 1-6°C. The label includes areas for donation identification and ABO label, storage instructions, reference number 136-62, lot number section, and manufacturer address in Covina, CA.*

FDA Label Image

Bag Label (Whole Blood 10)

Label for Leukotrap WB System, a CPDA-1 blood bag collection system by GVS TM Inc. It contains anticoagulant citrate phosphate dextrose adenine solution with specified concentrations per 70 mL. The bag is intended for whole blood storage at 1-6°C, marked for volunteer donors, and includes barcode, lot, and reference numbers.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.