Leukotrap Wb System - Cp2d Solution
Product Images NDC 87069-126

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Leukotrap Wb System - Cp2d (NDC 87069-126). 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

Ifu 1 (Ifu Page 1)

Diagram of the Leukotrap WB System - CP2D, an intravenous solution anticoagulant and additive system by GVS TM Inc. The illustration details components including satellite bag, additive/storage bag, collection bag, storage bag, WBF filter, sample diversion pouch, and connecting tubing with labeled parts and specifications.*

FDA Label Image

Ifu 2 (Ifu Page 2)

Instructions for blood collection using a system containing a sample diversion pouch with a pre-attached vacuum tube holder. The diagram shows a donor line setup including snap-open closure, Y-connector, phlebotomist protection device, clamp, sample diversion pouch, sample needle assembly with vacuum tube holder and lid, and donor needle. The text provides step-by-step procedures for accomplishing phlebotomy, collecting samples from the sample diversion pouch, blood collection precautions, discontinuing phlebotomy, and blood processing with filtration instructions.*

FDA Label Image

Ifu 3 (Ifu Page 3)

This image contains detailed instructions and notes for preparing and processing blood components using the Leukotrap WB System - CP2D, including filtration, centrifugation, plasma expression, transfer of additive solutions, and quality control testing. It also provides handling guidelines, storage conditions, and manufacturer contact information relevant for clinical laboratory settings.*

FDA Label Image

Pouch Label (Leukotrap 7)

Label for Leukotrap WB System - CP2D/AS-3, a solution for intravenous use. The label specifies a 500 ml double blood bag unit with CP2D/AS-3 and an in-line WBF filter and sampling system. Manufactured by GVS TM Inc, it includes detailed ingredient and composition information as well as storage instructions. The label also displays lot, quantity, and reference numbers along with barcodes.*

FDA Label Image

Case Label (Leukotrap 8)

Label for Leukotrap WB System CP2D/AS-3 Double Blood Bag Unit solution by GVS TM Inc, designed for collection of 500 mL whole blood. The sterile, nonpyrogenic system includes an in-line WBF filter and sampling system. The label shows the product quantity as 18 units and indicates storage instructions and lot information.*

FDA Label Image

Bag Label 3 (Plasma)

Label for Leukotrap WB System - CP2D by GVS TM Inc, intended for plasma collection from volunteer donors. The label includes the company address in Covina, CA, US, and displays symbols indicating sterility and prescription use. It specifies the reference number 126-62 and includes barcode and lot number fields.*

FDA Label Image

Bag Label 2 (Red Blood Cells 3)

Packaging label for Leukotrap WB System - CP2D by GVS TM Inc. The label indicates the product as a solution intended for intravenous use as an additive solution (AS-3) for red blood cells. It includes storage instructions (1-6°C), barcoding, reference number 126-62, and manufacturer details in Covina, CA, USA. The label also has space for donation ID and ABO label application.*

FDA Label Image

Bag Label 1 (Whole Blood 4)

Label for Leukotrap WB System - CP2D, a solution of anticoagulant citrate phosphate double dextrose with 3.57 g/70 mL strength, intended for whole blood collection. The label includes storage instructions (1–6 °C), manufacturer information (GVS TM Inc, Covina, CA), barcode, and usage warnings such as 'Do not transfuse unless ABO label applied.' Designed for intravenous use in human prescription drug applications.*

* 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.