Description

The NEOFLON PRO IV Cannula, also known as the BD Neoflon™ Pro Peripheral IV Catheter, is a specialized medical device designed for healthcare professionals seeking reliable vascular access. This sterile, single-use catheter is engineered for over-the-needle insertion, providing safe and efficient access to small and fragile blood vessels. It is particularly beneficial for neonatal, pediatric, and geriatric patients.

Key Features

• Versatile Use: Suitable for infusions, injections, blood transfusions, and pressure monitoring across various patient populations.
• Ergonomic Design: Features an anti-rotation tab and flexible wings for enhanced control and secure placement.
• Contamination Prevention: Equipped with a protection hub and Luer-lock connection for compatibility and safety.

Innovative Technologies

• BD Instaflash™ Needle Technology: Offers immediate visual feedback upon successful vessel entry, potentially reducing insertion attempts.
• BD Vialon™ Biomaterial: The polyurethane catheter softens significantly once in the vein, allowing longer dwell times and reducing mechanical phlebitis risk.
• Proprietary Lubrication and Tapered Tip: Ensures smoother, less painful insertion.

Safety Features

The advanced variant includes passive needle shield technology to protect against needlestick injuries, enhancing safety for healthcare providers.

Material Composition

• Catheter: Made from BD Vialon™ with radiopaque stripes for X-ray visibility.
• Hub and Wings: Constructed from polypropylene and polyethylene.
• Needle: Stainless steel.
• Free From: Phthalates, latex, BPA, animal-derived materials, and PVC.

Available Sizes

• 26 Gauge (Purple): 0.6 mm diameter, 19 mm length, 14 mL/min flow rate.
• 24 Gauge (Yellow): 0.7 mm diameter, 19 mm length, 19 mL/min flow rate.

Sterilization and Shelf Life

• Sterilization: Conducted using ethylene oxide, with a validated process.
• Shelf Life: Three years, with non-pyrogenic properties.

Storage Recommendations

• Temperature: 0–46°C, ideally at 25°C.
• No Special Conditions: No specific transportation or storage requirements.

Certifications and Standards

• CE Certified: Classified as a Class IIa medical device.
• Compliance: Adheres to multiple ISO standards for quality management, biocompatibility, and sterility.

Manufacturing Details

Produced by Becton Dickinson facilities in Sweden and Singapore, both ISO 13485 certified, ensuring high-quality manufacturing practices. Packaging includes multilingual labels compliant with European Medical Device directives, providing essential product information.

The NEOFLON PRO IV Cannula stands out for its advanced technology and design, offering healthcare professionals a dependable tool for effective and safe patient care.