Description

The VENFLON I IV Cannula by Becton Dickinson (BD Medical) is a highly specialized medical device designed for effective and safe venous access in various clinical settings. This sterile, single-use peripheral intravenous cannula is essential for healthcare professionals, facilitating the administration of fluids, medications, blood transfusions, and parenteral nutrition, as well as enabling blood sampling.

Key Features

• Needle-Free Injection Port: The integrated injection port and valve allow for seamless, needle-free administration of bolus medications during infusion, enhancing patient safety and convenience.
• Advanced Needle Design: Equipped with a back-cut needle bevel and tapered end, the cannula ensures easy insertion with minimal vein trauma, while the notched needle technology in some variants provides immediate visual confirmation of vessel entry.
• Secure Fixation: The winged design offers flexible wings for secure fixation, reducing the risk of bacterial contamination, and the color-coded wings and protection cap allow for quick size identification.
• Luer-Lock Fitting: Ensures a secure connection to IV lines and syringes, complemented by a flow control plug to prevent blood leakage.

Safety Features

• Passive Safety Needle System: Available in certain variants, this system shields the needle tip upon withdrawal, significantly reducing the risk of needlestick injuries.
• Ergonomic Design: The ergonomic hub provides a secure grip for ease of handling, and the beveled needle cap ensures safe disposal after use.

Material Composition

Crafted from high-quality materials, the catheter is made of polytetrafluoroethylene (PTFE) and siliconized for smooth insertion. The hub and wings are constructed from polypropylene, polyethylene, and polycarbonate, while the needle is stainless steel. Importantly, the device is not manufactured with natural rubber latex, phthalates, bisphenol A, or PVC, aligning with stringent safety standards.

Size and Packaging Options

The VENFLON I IV Cannula is available in various gauge options (14G to 22G) and lengths, with flow rates ranging from 31 to 270 mL/min. Each cannula is individually packaged in sterile units, with boxes containing 50 units and shipping cases of 500 units. The packaging complies with European Medical Device Directive labeling requirements.

Regulatory Compliance

This CE-certified Class IIa medical device meets comprehensive regulatory standards, including compliance with ISO 10993 for biocompatibility and EN ISO 11135-1 for sterilization. It is manufactured in India and designed to maintain sterility and performance over a five-year shelf life, with recommended storage conditions between 0–46°C.

Clinical Application and Maintenance

In clinical use, the cannula should be inserted using aseptic techniques, secured with a sterile dressing, and regularly flushed with saline. It is recommended to check and flush the device three times daily and remove it after 72 hours or as clinically indicated. As a single-use device, it must be disposed of safely after use, ensuring optimal patient care and safety.