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Invitation of quotation For Human Fibrin Sealant At All India Institute of Medical Sciences, Jodhpur Inquiry No.:: Aden/Gen/4411/2017AIIMS. Inquiry Issue Date:16th November, 2017Last Date of Submission:17th
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Step 1: Make sure the affected area is clean and dry.
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Step 2: Open the packaging of the human fibrin sealant.
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Step 3: Take out the required amount of fibrin sealant and place it on a sterile surface.
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Step 4: Use an appropriate applicator or syringe to apply the fibrin sealant directly to the wound or surgical site.
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Step 5: Ensure the fibrin sealant covers the entire area that needs sealing.
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Step 6: Gently press the edges of the wound or surgical site together to maximize adhesion.
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Step 7: Allow the fibrin sealant to dry completely before applying any dressings or bandages.
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Step 8: Dispose of any unused fibrin sealant according to proper medical waste protocols.

Who needs human fibrin sealant?

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Human fibrin sealant is commonly used by healthcare professionals during surgeries or medical procedures.
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It is primarily used for patients who have excessive bleeding or need tissue sealing.
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This may include individuals undergoing cardiovascular, general, or orthopedic surgeries, as well as those with certain types of wounds or injuries.
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Ultimately, the decision to use human fibrin sealant is made by a medical professional based on the specific needs of the patient.
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Human fibrin sealant is a biological product used for medical purposes to aid in the clotting of blood and tissue sealing during surgical procedures.
Manufacturers or distributors of human fibrin sealant are required to file with the appropriate regulatory authorities.
The filing process for human fibrin sealant typically involves submitting detailed information about the product, its components, manufacturing process, and safety data to regulatory agencies.
The purpose of human fibrin sealant is to assist in hemostasis (control of bleeding) and tissue sealing during surgical procedures, reducing the risk of excessive blood loss and promoting wound healing.
Information such as product composition, manufacturing process, safety data, quality control measures, and intended use must be reported on human fibrin sealant.
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