BD Neoflon™ Pro IV Catheter 24GA x 0.75\ (0.7 x 19 mm) – Box of 50
Becton Dickinson
Medical device – peripheral intravenous catheter
Non-ported straight peripheral IV cannula for paediatric/neonatal use
Certifications
CE Marked medical device (Class IIa, region dependent).
Manufactured under an ISO 13485–certified quality management system for medical devices.
Complies with relevant standards for intravascular catheters (such as ISO 10555 series) and luer connections.
Sterile, non Pyrogenic, single Use device in accordance with applicable infusion therapy and infection control standards.
CE Marked medical device (Class IIa, region dependent).
Manufactured under an ISO 13485–certified quality management system for medical devices.
Complies with relevant standards for intravascular catheters (such as ISO 10555 series) and luer connections.
Sterile, non Pyrogenic, single Use device in accordance with applicable infusion therapy and infection control standards.
Non-ported straight peripheral IV cannula for paediatric/neonatal use
Description
The BD Neoflon™ Pro IV Catheter 24GA x 0.75\ (0.7 x 19 mm) is a peripheral intravenous cannula designed to access smaller, more fragile vessels with care and precision, particularly in paediatric and neonatal patients. It is a straight, non-ported IV catheter made from proprietary BD Vialon™ biomaterial, which softens in the vein to enhance patient comfort, allow longer dwell times and help reduce the risk of mechanical phlebitis. The device incorporates BD Instaflash™ technology in the introducer needle, providing immediate visual confirmation of vessel entry to support first-attempt success. The 24G (yellow) catheter is supplied as a box of 50 sterile, single-use cannulas, each with an ergonomically designed hub for secure grip and precise control during insertion.
Bnefits
Specially designed 24G x 19 mm straight IV catheter to access smaller, fragile vessels in paediatric and neonatal patients.
Catheter made from BD Vialon™ biomaterial, which softens once in the vein, improving comfort, allowing longer dwell times and helping to reduce mechanical phlebitis.
BD Instaflash™ needle technology provides rapid visual confirmation of vessel entry via an immediate blood flashback, supporting first-stick success.
Non-ported design with straight cannula construction simplifies line management in small patients and reduces potential sites of contamination.
Ergonomically shaped hub and stable grip surfaces to aid controlled insertion and secure handling even in challenging access situations.
Colour-coded yellow hub for easy identification of 24G size and quick selection in busy clinical environments.
Compatible with standard luer-lock IV administration sets and accessories for infusion therapy and medication delivery.
Sterile, non-pyrogenic, single-use device to support infection prevention and patient safety.
Available in boxes of 50 cannulas to support routine use in hospitals, paediatric wards, neonatal units, emergency departments and specialist clinics.
Indications
Peripheral intravenous cannulation in paediatric, neonatal and other patients with small or fragile veins where a 24G catheter is clinically appropriate.
Short-term administration of IV fluids, medications and electrolytes via peripheral veins.
Peripheral blood sampling through an indwelling cannula when permitted by local protocols and device labelling.
Use in hospital, emergency, theatre, day-case and outpatient settings that require reliable small-gauge IV access.
Supportive IV access in aesthetic and dermatology practice when peripheral cannulation is required for fluid administration or adjunctive therapies.
Composition
Catheter: BD Vialon™ polyurethane biomaterial, 24G (0.7 mm outer diameter) x 19 mm length (0.75 inch).
Introducer needle: stainless steel bevelled IV needle with BD Instaflash™ flashback technology.
Hub: colour-coded yellow polymer hub to indicate 24G gauge, with ergonomic grip design.
Protective needle cover: rigid polymer shield to maintain needle sterility prior to use.
Device configuration: non-ported, straight peripheral IV cannula with standard luer-lock connection to IV sets.
Sterility: sterile, non-pyrogenic, single-use medical device supplied ready for clinical use.
Formulation
Peripheral IV catheter, 24G x 0.7 mm x 19 mm (0.75 inch), non-ported, straight cannula constructed from BD Vialon™ biomaterial with stainless steel introducer needle and BD Instaflash™ technology, sterile and non-pyrogenic, intended for single use only.
Packaging
Box of 50 individually packaged BD Neoflon™ Pro IV Catheters (24G x 0.75").
Each catheter supplied in a sterile, peel-open blister or pouch with protective needle cover and clearly printed product identification, gauge and lot number.
Outer carton labelled with BD Neoflon™ Pro branding, reference number 391380, gauge (24G), catheter length (19 mm / 0.75"), yellow colour coding, sterility status, expiry date, and regulatory markings including CE mark (where applicable).
Packaging designed for convenient storage in clinical areas such as paediatric wards, NICU, emergency and theatre environments.
Usage
Verify that the product, gauge (24G) and length (19 mm) are appropriate for the intended patient and procedure before use.
Inspect the package for damage and check the expiry date; do not use if packaging is opened, damaged or expired.
Prepare the patient and intended insertion site using aseptic technique and local clinical protocols.
Remove the catheter from its sterile packaging, maintaining sterility of the catheter and needle.
Stabilise the target vein and insert the BD Neoflon™ Pro IV Catheter with bevel up at an appropriate angle, observing for flashback via BD Instaflash™ technology to confirm vessel entry.
Advance the catheter into the vein according to institutional protocol while withdrawing the introducer needle, taking care not to reinsert the needle into the catheter once withdrawn.
Connect the catheter hub to the prescribed IV administration set, extension line or injection cap via the luer-lock connection and secure the cannula with appropriate fixation and dressing.
Regularly assess the site for signs of infiltration, phlebitis, infection or occlusion and follow institutional guidelines for dwell time and line care.
On completion of therapy or if complications occur, remove the catheter according to local procedures and discard the entire device as sharps/clinical waste; do not reuse.
Contraindications
Do not use in patients with a known hypersensitivity or allergy to any component of the device (e.g. polyurethane or stainless steel).
Contraindicated for arterial cannulation, central venous access or any application not consistent with a peripheral IV catheter.
Do not insert the cannula into areas with active infection, inflammation, burns or significant skin compromise.
Not intended for reuse; reuse of single-use IV catheters significantly increases the risk of infection, catheter damage and device failure.
Do not reinsert a partially or fully withdrawn needle into the catheter, as this may damage the catheter and increase the risk of embolisation or catheter failure.
Adverse Effects
Local complications at the insertion site, including pain, redness, swelling, bruising, infiltration or extravasation of infusate.
Phlebitis or thrombophlebitis, particularly if dwell times exceed recommended limits or site care protocols are not followed.
Infection or sepsis associated with poor aseptic technique or prolonged cannula dwell time.
Catheter occlusion or malfunction requiring replacement of the device.
Rare risk of catheter breakage or embolisation if misused or if the needle is reinserted into the catheter.
Systemic complications such as air embolism or fluid overload if IV therapy is not managed correctly.
Storage Conditions
Store in a clean, dry environment at room temperature, away from direct sunlight and extremes of heat or cold.
Keep in original packaging until point of use to maintain sterility.
Do not use if packaging is wet, torn or otherwise compromised, or if the product is past its expiry date.
Protect from crushing, bending or other mechanical damage that could affect device performance.
Store out of reach of unauthorised persons and children.
