Description

The VENFLON I IV Cannula, crafted by Becton Dickinson (BD), is a specialized medical device designed for effective peripheral intravenous access. This sterile, single-use catheter is essential for healthcare professionals, providing reliable access to peripheral veins for various medical needs such as rehydration, medication delivery, blood transfusion, and parenteral nutrition.

Key Features

• Size and Color Coding: The cannula is sized at 22G x 25 mm (1.00 inch) and is color-coded blue for easy identification.
• Winged Design: Its winged design enhances stability and minimizes the risk of bacterial contamination, ensuring safer insertion.
• Needle Design: Equipped with a back-cut needle bevel, it allows for smoother insertion and reduces the risk of vein damage.
• Catheter Material: Made from PTFE, the catheter is soft and siliconized, promoting easier insertion and greater patient comfort.

Integrated Injection Port

The VENFLON I IV Cannula features an integrated injection port with an automatic valve, allowing for needle-free administration of bolus medications during infusion. This design includes BD Luer-Lok compatibility for secure connections, enhancing overall safety and convenience.

Additional Features

• Flow Control Plug (FCP): Indicates venous entry and prevents blood leakage.
• Flexible Wings: Provides secure fixation and improved patient comfort.
• Protection Hub: Reduces contamination risks.
• Passive Safety System: Available in some variants, offering a needle protection system to minimize needlestick injuries.
• Visual Confirmation: Some variants include a notched needle for immediate vessel entry confirmation using BD Instaflash™ Needle Technology.

Material and Biocompatibility

The materials used include polypropylene, polyethylene, polycarbonate, PTFE, stainless steel, and silicone. The device is not formulated with natural rubber latex, phthalates, bisphenol A, PVC, or blood derivatives, ensuring broad biocompatibility. It meets ISO 10993 standards for toxicity, pyrogenicity, and biocompatibility.

Sterilization and Compliance

Sterilized using ethylene oxide and validated per EN ISO 11135-1, the cannula is CE marked under the Medical Devices Directive 93/42/EEC, Class IIa. It complies with relevant ISO standards for sterility, labeling, conical fittings, and quality management.

Packaging and Shelf Life

Each cannula is individually packed, with 50 units per shelf box and 500 units per shipping case. It features multilingual labeling compliant with the European Medical Device Directive. The product boasts a shelf life of 5 years and is recommended to be stored at temperatures between 0–46°C, ideally at 25°C.

Usage and Handling

Designed for single use, the VENFLON I IV Cannula remains sterile until opened or damaged. It is a vital tool in medical settings, offering secure and efficient intravenous access while minimizing common risks such as infection and blood clot formation.