Description

The VENFLON I IV Cannula by Becton Dickinson (BD) is a highly specialized medical device designed for secure and efficient peripheral intravenous access. This sterile, single-use cannula is essential for healthcare settings, facilitating tasks such as rehydration, parenteral nutrition, medication delivery, blood transfusion, and patient monitoring.

Key Features

• Integrated Injection Port and Valve: Enables needle-free administration of medications, enhancing safety and convenience during infusion.
• Passive Safety Needle System: Provides comprehensive needle tip shielding upon withdrawal, significantly reducing the risk of needlestick injuries.
• Back-Cut Needle Bevel: Ensures smoother insertion with minimal vein damage, complemented by a tapered catheter end to reduce trauma.
• Flexible Wings: Assist in secure placement and minimize contamination risks by preventing direct contact with the skin.

Design and Technology

The cannula features color-coded protection caps for easy gauge identification, adhering to ISO standards. The Flow Control Plug (FCP) indicates vein entry and prevents blood leakage, while the ported design with a snap cap prevents accidental openings. Select variants include BD Instaflash™ Needle Technology, offering immediate visual confirmation of vessel entry.

Material Composition

Crafted from BD Vialon™ polyurethane, the catheter softens within the vein, promoting longer dwell times and reducing phlebitis. Other components are made from high-quality materials such as polypropylene, polyethylene, and stainless steel, ensuring durability and performance.

Biocompatibility and Safety

The device is latex-free, DEHP-free, PVC-free, and BPA-free, aligning with stringent safety standards. It is non-pyrogenic and contains no animal tissue, mitigating any TSE/BSE risks. Sterilized using ethylene oxide or radiation, the cannula complies with EN ISO standards, offering a shelf life of 3 to 5 years.

Certification and Compliance

The VENFLON I IV Cannula is a CE-certified Class IIa medical device, adhering to the Medical Devices Directive 93/42/EEC. It meets various ISO standards, ensuring biocompatibility and performance as an intravascular catheter.

Packaging and Instructions

Available in multiple gauge sizes and lengths, each cannula is individually packed in medical-grade materials. Packaging includes multilingual labels and comprehensive instructions for use, emphasizing aseptic techniques and safe disposal after single use.

Clinical Application

This device is a reliable choice for healthcare professionals, offering robust performance and enhanced safety features for effective intravenous therapy management.