BD IV Cannula Dressing Veca C, Box of 50

Becton Dickinson

Medical device – IV fixation dressing

Sterile semi-permeable transparent IV cannula fixation dressing

CE Marked sterile fixation dressing for intravenous cannulae under applicable EU and UK medical device regulations.
Manufactured under an ISO 13485 Certified quality management system for medical devices.
Materials assessed for biocompatibility in line with ISO 10993 series standards for externally applied devices with breached or compromised surfaces.
Sterilisation process validated to an appropriate sterility assurance level according to recognised ISO/EN standards for terminally sterilised single Use medical devices.
Latex Free construction in accordance with BD labelling to minimise the risk of natural rubber latex sensitisation.

CE Marked sterile fixation dressing for intravenous cannulae under applicable EU and UK medical device regulations.
Manufactured under an ISO 13485 Certified quality management system for medical devices.
Materials assessed for biocompatibility in line with ISO 10993 series standards for externally applied devices with breached or compromised surfaces.
Sterilisation process validated to an appropriate sterility assurance level according to recognised ISO/EN standards for terminally sterilised single Use medical devices.
Latex Free construction in accordance with BD labelling to minimise the risk of natural rubber latex sensitisation.

Sterile semi-permeable transparent IV cannula fixation dressing

Description

BD IV Cannula Dressing Veca-C is a sterile, single-use, latex-free fixation dressing specifically designed to protect and secure peripheral intravenous cannulas. Suitable for both ported and non-ported IV cannulae, the dressing is made from a transparent, semi-permeable adhesive film with an integrated wound pad and comfort pad. The semi-permeable structure allows moisture vapour and oxygen transmission so the insertion site can breathe, while providing an effective barrier to bacteria and external contaminants. The integrated absorbent pad helps manage exudate and keeps the puncture site dry, and the compressed comfort pad is designed to be placed under the cannula wings to enhance patient comfort and reduce pressure. A clear polyurethane window allows continuous visual inspection of the catheter track and insertion site for early signs of phlebitis or infection. BD Veca-C dressings are individually packaged and intended for short-term fixation of IV catheters in hospital, clinic and community care settings.

Bnefits

Provides effective fixation for both ported and non-ported IV cannulas, helping to maintain catheter stability and reduce the risk of dislodgement.
Transparent, semi-permeable film allows the insertion site to breathe while providing a barrier to bacteria and external contaminants.
Integrated wound pad absorbs exudate at the catheter insertion site, helping to keep the area dry and more comfortable for the patient.
Compressed comfort pad is designed to be placed under the wings of the IV cannula to reduce pressure points and enhance patient comfort.
Transparent viewing window made of polyurethane enables continuous visual inspection of the puncture site and catheter track for early detection of phlebitis or infection.
Sterile, single-use construction supports infection prevention and reduces cross-contamination risk between patients.
Latex-free materials help minimise the risk of latex-related hypersensitivity reactions.
Adhesive border provides secure fixation while allowing relatively atraumatic removal when the dressing needs to be changed.
Designed specifically for peripheral catheter fixation, offering a tailored shape and pad arrangement compared with generic adhesive dressings.
Compatible with standard peripheral IV catheter sizes and commonly used insertion sites in adult and appropriate paediatric patients.

Indications

Fixation and protection of peripheral intravenous cannulas (ported and non-ported) at the insertion site.
Use as a sterile dressing over IV catheter puncture sites to maintain a clean environment and reduce infection risk.
Clinical situations requiring regular visual inspection of the catheter track and insertion site through a transparent window.
Short-term fixation of IV cannulas in hospital wards, emergency departments, operating theatres, day-case units and community or outpatient settings.

Composition

Backing material: Transparent semi-permeable polyurethane or similar film that allows moisture vapour and oxygen transmission while acting as a barrier to liquids and microorganisms.
Adhesive: Medical-grade pressure-sensitive adhesive suitable for skin contact, providing secure fixation while allowing atraumatic removal when used as directed.
Wound pad: Absorbent pad located over the insertion site to take up exudate and help keep the puncture area dry.
Comfort pad: Compressed pad intended to be placed under the wings of the IV catheter to reduce local pressure and improve patient comfort.
Viewing window: Clear polyurethane window integrated into the dressing to allow direct visual inspection of the catheter track and insertion site.
Release liner: Protective liner covering the adhesive surface prior to application, removed immediately before use.
Materials status: Latex-free construction; natural rubber latex is not intentionally used in the dressing or primary packaging.

Formulation

Device type: Sterile IV cannula fixation dressing (film dressing with pad and comfort pad).
Typical dimensions: Approximately 7–7.5 cm x 6–9 cm overall size, designed to accommodate standard peripheral IV cannulas (exact size may vary slightly by regional code).
Structure: Semi-permeable adhesive film with integrated absorbent wound pad, comfort pad for placement under cannula wings, and transparent viewing window to monitor catheter track.
Permeability: Semi-permeable to moisture vapour and gases while impermeable to liquids and bacteria under normal use conditions.
Sterility: Terminally sterilised, supplied sterile for single use only.
Fixation area: Adhesive border around pads and window to secure the cannula and dressing to the patient’s skin.
Compatibility: Designed for use with standard peripheral IV catheters from BD and other manufacturers, for both ported and non-ported cannula designs.

Packaging

Primary packaging: Individual sterile packs containing one BD Veca-C IV cannula dressing per pouch.
Box configuration: Box of 50 individually packaged dressings.
Outer labelling: Box labelled with product name (BD IV Cannula Dressing Veca-C), description (sterile fixation dressing for intravenous cannula), BD branding, quantity (50), SKU (392020 or equivalent), lot number, expiry date, sterility and single-use symbols, and regulatory marks.
Sterility maintenance: Packaging designed to maintain sterility of each dressing until the individual pouch is opened immediately before use.
Shipping: Boxes may be supplied in outer cartons for transport and storage according to distributor and facility requirements.

Usage

Verify that the sterile pouch is intact and within its expiry date before use. Do not use if the pouch is damaged, open or expired.
Perform hand hygiene and don appropriate personal protective equipment according to institutional infection prevention policies.
Prepare and insert the IV cannula using aseptic technique, following local guidelines for site selection, skin preparation and cannulation.
Ensure the insertion site and surrounding skin are clean and dry before applying the dressing. If necessary, gently dry the skin with sterile gauze after antiseptic solution has fully dried.
Open the sterile pouch and remove the BD Veca-C dressing using aseptic technique, taking care not to touch the adhesive surface with non-sterile hands or objects.
Position the compressed comfort pad under the wings of the IV cannula, if not pre-positioned, to provide cushioning between the catheter wings and the skin.
Align the wound pad so that it covers the catheter puncture site, ensuring the insertion site is centred beneath the absorbent pad.
Apply the transparent adhesive film over the cannula, wings and pads, smoothing from the centre outward to eliminate wrinkles and air pockets while ensuring good adhesion to the surrounding skin.
Make sure the transparent window overlies the catheter track so the insertion site and surrounding vein path can be visually inspected through the dressing.
Secure any associated tubing and connectors according to local protocols, using additional tape or securement devices if required to minimise catheter movement.
Inspect the site regularly for signs of phlebitis, infection, infiltration or dressing edge lift. Replace the dressing if it becomes loose, visibly soiled, wet, or if the integrity is compromised.
When changing the dressing, carefully peel back the adhesive film while supporting the skin and cannula to avoid catheter dislodgement. Dispose of used dressings in accordance with local clinical waste policies.

Contraindications

Do not apply to patients with known hypersensitivity or allergy to any of the dressing components (e.g., adhesive, film, pad materials).
Do not apply over infected, heavily exuding, bleeding or severely compromised skin without appropriate clinical evaluation and alternative dressing selection.
Not intended for use as a primary dressing on large open wounds or surgical incisions separate from an IV cannula site.
Do not use if the sterile pouch is opened or damaged before intended use.
Do not reuse or resterilise; single-use only.

Adverse Effects

Local skin irritation, itching, redness or rash related to adhesive sensitivity or contact dermatitis.
Maceration of the skin under the dressing if moisture accumulates and dressing changes are not performed as needed.
Blistering or skin stripping upon removal, particularly in patients with fragile or compromised skin if removal is not performed carefully.
Rare allergic reactions to dressing materials, potentially requiring discontinuation and selection of an alternative product.
If the dressing is not applied or maintained correctly, there may be an increased risk of catheter-related infection or dislodgement due to inadequate fixation rather than the dressing itself.

Storage Conditions

Store in a cool, dry place in the original packaging until use.
Protect from direct sunlight, excessive heat and moisture.
Avoid crushing or bending the box to prevent damage to individual sterile pouches.
Do not use after the expiry date printed on the packaging.
Keep out of the reach of children and unauthorised personnel.

Duration

Intended for short-term use as part of peripheral IV cannula fixation. Dressing wear time is determined by institutional policy, condition of the dressing, and clinical assessment of the insertion site, but typically ranges from 24 to 72 hours or longer if the dressing remains clean, dry, intact and the site is uncompromised.

Onset

Provides immediate fixation and protection of the IV cannula and insertion site upon correct application of the dressing. Infection prevention benefits depend on continued integrity of the dressing and adherence to aseptic technique.