Intersol Solution
Product Images NDC 0942-9601

This text appears to be a table showing the mean and standard deviation for various parameters assessed in vitro, including glucose and lactate levels, as well as measurements of lactate dehydrogenase and morphology scores. It also includes measurements related to hypothermic shock response and extent of shape changes.*

Table 3 provides the measured parameters for both irradiated and non-irradiated platelets in an in vitro assessment. The parameters include glucose, lactate, GO, bicarbonate, lactate dehydrogenase, GDG2 expression, morphology score, hypotonic shock response, and extent of shape change. The mean and standard deviation for each parameter are also provided for each day measured.*

InterSol Solution Platelet Additive Solution 3 is a solution for use with the AMICUS separator only, to preserve platelets, manufactured by Fenwal International Inc., Puerto Rico, and imported and distributed by Fresenius Kabi Colombia. It contains dibasic sodium phosphate, monobasic sodium phosphate, sodium citrate, sodium acetate, sodium chloride, and water for injection, USP. It is sterilized by a combination of steam and radiation and has a nonpyrogenic fluid path. The solution should not be used for direct intravenous infusion. The package includes manufacturing company, manufacturing facility, lot number, and other essential instructions.*

This appears to be a cautionary message for a medical product, specifically a Platelet Additive Solution. The product has been sterilized using steam and radiation and has a sterile fluid path. The instructions for use are important and should be consulted before using the product. The text warns against reusing the product or venting it. If the instructions are not followed, the sterility of the product may be compromised.*

This is a description of a medical product with cautionary instructions. The product is sterilized using a combination of steam and radiation, and has a sterile fluid path. The fluid path is non-pyrogenic but reusing the product is not recommended if the product's sterile barrier system is compromised. The product has multiple codes including lot and expiration dates, and information about the manufacturer and manufacturing facility. It is marked as fragile and has instructions to handle carefully to avoid accidentally cutting into the package. The packaging can be recycled, but venting is not allowed. The product is a Platelet Additive Solution and is restricted by US federal law for sale by or on the order of a licensed healthcare practitioner.*