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The B Braun Introcan IV Catheter is a medical device designed for establishing peripheral venous access. It facilitates the administration of intravenous fluids, medications, and blood products by providing a secure pathway into a patient's circulatory system. This catheter is constructed from FEP (Fluorinated Ethylene Propylene), a medical-grade polymer known for its flexibility and biocompatibility, which helps to minimize patient discomfort during insertion and while in situ.
The device is intended for single-use applications to maintain sterility and prevent cross-contamination.
This IV catheter functions by utilizing a sharp, beveled needle to penetrate the vein. Once venous access is achieved, the needle is withdrawn, leaving the flexible catheter in place. The catheter's design incorporates a radiopaque stripe, allowing for visualization under X-ray imaging, which aids in confirming correct placement and assessing the catheter's position within the vessel.
The hub of the catheter features a Luer Lock connection, ensuring a secure and leak-free attachment for infusion sets, syringes, and other Luer-compatible medical devices. The pink color-coding of the hub indicates a 20-gauge size, with a length of 32 mm and a diameter of 1.1 mm, suitable for a range of clinical applications.
Key features of the Introcan IV Catheter include its FEP catheter material, which offers a balance of rigidity for insertion and flexibility for patient comfort. The sharp beveled needle tip is engineered for smooth venipuncture, reducing the likelihood of vessel trauma. The integrated safety mechanism is designed to prevent accidental needlestick injuries post-insertion, enhancing healthcare professional safety.
The Luer Lock connector provides a reliable method for securing connections to prevent dislodgement and maintain the integrity of the infusion line. The radiopaque marking is crucial for accurate placement verification in diagnostic imaging procedures.
This product is utilized by a variety of healthcare professionals, including nurses, physicians, and other trained medical personnel in diverse clinical settings. Patients requiring intravenous therapy for hydration, medication delivery, or nutritional support are the end-users of the access provided by this catheter. Caregivers may also be involved in managing the catheter site under the guidance of medical professionals.
Typical applications include short-term intravenous access for fluid resuscitation, antibiotic administration, chemotherapy, pain management, and blood transfusions in hospital wards, emergency departments, intensive care units, and outpatient clinics.
Important usage notes include ensuring the integrity of the packaging before use; the device is sterile and intended for single use only. It should not be reused or resterilized. Proper aseptic technique must be employed during insertion to minimize the risk of infection.
Following insertion, the catheter should be secured according to institutional protocols to prevent dislodgement. The catheter should be removed promptly when no longer clinically indicated to reduce the risk of complications such as phlebitis or infection. Storage should be in a cool, dry environment away from direct sunlight.
This device is not intended for use by children without appropriate medical supervision.

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