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BD Saf T Intima Pink 20G x 1.0\ Closed IV Catheter System with Removable PRN Adapter

BD Saf T Intima Pink 20G x 1.0\ Closed IV Catheter System with Removable PRN Adapter

Becton Dickinson

Medical device
  • Manufactured by BD in facilities operating under an ISO 13485:2016 Certified quality management system
  • Sterile, single Use medical device
  • Latex Free construction
Peripheral IV catheter / closed IV catheter system

Description

BD Saf-T-Intima Pink 20G x 1.0\ with removable PRN adapter is a closed peripheral IV catheter system designed for patients with difficult venous access, such as oncology and chronically ill patients. The device integrates a 20-gauge, 1.0-inch BD Vialon catheter with soft butterfly-style wings, preattached extension tubing and a removable PRN (port) adapter in a single, low-profile system. An automated safety mechanism fully encapsulates the needle after use to help minimise needlestick injuries and blood exposure. The BD Vialon biomaterial and integrated, flexible wings improve catheter stabilisation, help reduce mechanical irritation and can support longer dwell times compared with traditional Teflon catheters. The pink colour coding identifies the 20G size and allows quick selection in clinical environments. Each catheter is supplied sterile in an individual blister pack, with 25 catheters per box.

Bnefits

  • Integrated closed IV catheter system combining catheter, wings, extension tubing and PRN adapter in one device
  • Designed for difficult veins, particularly in oncology and other patients with challenging vascular access
  • Automated in-built safety mechanism that fully encapsulates the needle after use to minimise needlestick injuries
  • Closed system design helps reduce blood exposure and contamination risk during insertion and connection
  • BD Vialon catheter biomaterial improves softness and flexibility in the vessel, supporting longer dwell times vs traditional Teflon catheters
  • Large, soft wings and integrated extension tubing enhance catheter stabilisation and patient comfort
  • 20G x 1.0" size provides a good balance of flow rate and patient comfort for many IV therapies
  • Pink colour-coded hub clearly identifies gauge for quick, correct product selection
  • Latex-free, sterile, single-use device to support infection prevention and patient safety
  • Individually packaged in easy-to-open blisters to maintain sterility and simplify clinical handling

Indications

  • Peripheral intravenous (IV) cannulation for short- to medium-term therapy
  • Subcutaneous or IV infusion when using an integrated Saf-T-Intima system as clinically indicated
  • Administration of IV fluids, medications and blood products according to local protocols
  • Vascular access in oncology patients and others with difficult or fragile veins
  • Situations where reduced blood exposure and needlestick injury risk are a priority

Composition

  • Catheter: BD Vialon biomaterial (polyurethane-based thermoplastic)
  • Needle: stainless steel
  • Wings: soft, flexible polymer
  • Extension tubing: medical-grade polymeric tubing with integrated PRN adapter
  • Latex-free construction

Formulation

  • 20G (1.1 mm) over-the-needle catheter, 1.0 inch (25 mm) length
  • Integrated extension set with removable PRN adapter
  • Closed IV catheter system with passive/automatic needle safety mechanism
  • Butterfly-style wings for fingertip control during insertion
  • Sterile, single-use, non-pyrogenic device

Packaging

  • Box of 25 catheters
  • Each catheter individually packaged in a sterile blister pack
  • Outer carton labelled with gauge, length, colour code (pink), lot number and expiry date

Usage

  • Verify product integrity and expiry date; do not use if packaging is damaged or expired.
  • Prepare and disinfect the insertion site according to local infection control protocols.
  • Prime the extension tubing and PRN adapter if required by local practice, maintaining sterility.
  • Using the butterfly wings for fingertip control, insert the needle and catheter into the vessel at an appropriate angle until blood return confirms venous access.
  • Advance the catheter into the vessel while withdrawing the needle according to manufacturer instructions.
  • Activate the automated safety mechanism to fully encapsulate the needle and reduce needlestick risk, keeping hands behind the needle tip.
  • Secure the catheter and wings to the skin with appropriate dressings and fixation devices.
  • Connect the PRN adapter to IV tubing, injection caps or other approved accessories as required, and flush according to protocol.
  • Monitor the insertion site regularly for signs of infiltration, phlebitis, leakage or infection.
  • Dispose of the used needle-containing safety device and all packaging in an approved sharps or clinical waste container.

Contraindications

  • Do not use in patients with known hypersensitivity or allergy to any component materials of the device.
  • Avoid insertion into limbs or areas with compromised circulation, infection, thrombosis, burns or significant oedema.
  • Do not use for arterial puncture or in locations not suitable for peripheral IV or subcutaneous access.
  • Do not reuse; single-use device only.

Adverse Effects

  • Local pain, bruising or discomfort at the insertion site
  • Infiltration or extravasation of infused fluids
  • Phlebitis or thrombophlebitis
  • Local or systemic infection if aseptic technique is not followed
  • Hematoma formation or bleeding at the insertion site
  • Allergic or hypersensitivity reactions to device materials

Storage Conditions

  • Store in original packaging in a clean, dry environment.
  • Keep at room temperature away from excessive heat, moisture and direct sunlight.
  • Do not use if the sterile package is opened, damaged or wet.
  • Observe the expiry date on the packaging and do not use beyond this date.

Duration

Intended for short- to medium-term peripheral IV or subcutaneous access; actual dwell time depends on clinical indication, vein condition and local vascular access policies.

Onset

Provides immediate IV or subcutaneous access for therapy once the catheter is successfully inserted and connected.

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