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Introcan Safety Catheter Range

Introcan Safety Catheter Range

Introcan Safety

Injection & Infusion
  • CE Marked peripheral IV catheter (medical device)
  • Manufactured according to ISO 10555 1/5 for intravascular catheters
  • Latex Free, PVC Free, DEHP Free construction
Peripheral IV Catheter

Description

Introcan Safety PUR 24G 0.7 x 19mm is a peripheral IV catheter made from soft polyurethane (PUR) with an integrated passive, fully automatic safety shield to reduce needlestick injuries. The non-ported, straight catheter is designed for single-use intravascular and tissue access to sample blood, monitor blood pressure, or administer fluids and blood, and is also suitable for subcutaneous infusion therapies and power injector applications up to 300 psi (sizes 18–24G). This 24G version (0.7 mm diameter, 19 mm/0.75\ length) is supplied as a box of 50 catheters.

Bnefits

  • Passive Safety Shield that activates automatically on needle withdrawal to reduce needlestick injuries and related infections
  • Stabilization platform that improves catheter stability and minimizes movement within the vessel
  • Multi-access septum that helps control blood flow and reduces blood leakage and clean-up time
  • Double Flashback Technology providing visual confirmation that both needle and catheter are correctly placed in the vessel, improving first-stick success
  • Universal back-cut bevel allowing a wide choice of insertion angles and aiding access to difficult veins with reduced puncture trauma
  • Radiopaque catheter stripes for good visibility under X-ray
  • Pressure-rated for contrast media power injection up to 300 psi (18–24G)
  • Soft polyurethane catheter material for more comfortable in-dwelling performance compared with more rigid materials
  • Latex-free, PVC-free and DEHP-free construction for reduced risk of material-related reactions
  • Single-use, sterile design supporting best practice infection control
  • Available in a range of sizes from 24G to 14G for different clinical requirements

Indications

  • Peripheral intravascular access for infusion of fluids, blood and medications
  • Blood sampling via peripheral IV access when clinically appropriate
  • Non-invasive blood pressure monitoring via arterialised or appropriate IV access where indicated
  • Subcutaneous infusion therapies as per clinical protocols
  • Use with power injectors for contrast media up to 300 psi (sizes 18–24G)
  • Use in adults, paediatrics and neonates where peripheral IV therapy is prescribed

Composition

  • Catheter material: Polyurethane (PUR) peripheral IV catheter with radiopaque stripes
  • Needle: Stainless steel with universal back-cut bevel and integrated passive safety shield
  • Hub and stabilisation platform: Injection-moulded medical-grade polymer with push-off plate
  • Multi-access septum and vented flash plug assembly for controlled blood flow and connection
  • Latex-free, PVC-free, DEHP-free materials

Formulation

  • Sterile, non-pyrogenic, single-use peripheral IV catheter
  • Polyurethane (PUR) catheter with integrated passive safety mechanism and non-ported, straight hub

Packaging

  • Box of 50 Introcan Safety PUR 24G 0.7 x 19mm IV catheters
  • Each catheter supplied in individual sterile blister packaging with protective needle cover and instructions

Usage

  • For use only by trained healthcare professionals familiar with peripheral IV cannulation techniques.
  • Verify the integrity of the sterile packaging and confirm expiry date before use; do not use if packaging is damaged or expired.
  • Prepare equipment according to local protocol and select an appropriate vein for cannulation.
  • Disinfect the skin at the intended insertion site using approved antiseptic in accordance with infection control guidelines.
  • Remove the catheter from its packaging, maintaining aseptic technique, and position the bevel for insertion at the chosen angle.
  • Insert the catheter/needle assembly into the vein; observe first needle flashback in the flashback chamber and second flashback in the catheter segment to confirm vessel entry (Double Flashback Technology).
  • Advance the catheter into the vessel while withdrawing the needle according to standard IV cannulation practice; the passive safety shield will automatically cover the needle tip upon withdrawal.
  • Stabilise the catheter using the stabilisation platform and secure it to the skin with appropriate dressings and securement devices.
  • Attach IV tubing or accessories as needed and flush the catheter to confirm patency, following local policies.
  • Monitor the site regularly for signs of infiltration, phlebitis, infection or dislodgement and replace the catheter in accordance with institutional and clinical guidelines.
  • Dispose of the needle and packaging in approved sharps and clinical waste containers immediately after use.

Contraindications

  • Do not insert into areas of active infection, inflammation, burns or skin lesions.
  • Avoid use in limbs or sites where venous or lymphatic flow is compromised, unless specifically indicated.
  • Do not use in patients with known hypersensitivity to polyurethane, stainless steel, or any component of the device.
  • Not intended for central venous access or arterial cannulation unless specifically indicated by the manufacturer and local protocol.
  • Do not reuse; single-use only.

Adverse Effects

  • Local pain, discomfort, or bruising at the insertion site.
  • Infiltration or extravasation of infusate into surrounding tissue.
  • Phlebitis (vein inflammation) or thrombophlebitis.
  • Local or systemic infection if aseptic technique is not adhered to or catheter is left in situ beyond recommended dwell time.
  • Hematoma formation due to vessel trauma.
  • Allergic or hypersensitivity reactions to device materials (rare).
  • Very rare risk of catheter-related bloodstream infection or embolism if misused or not managed according to guidelines.

Storage Conditions

  • Store in a clean, dry place at room temperature, away from excessive heat and direct sunlight.
  • Keep in original packaging until point of use to maintain sterility.
  • Do not use if packaging is damaged, opened, or wet.
  • Keep out of reach of children.

Duration

Intended for short- to medium-term peripheral IV access; dwell time should follow institutional policies and clinical guidelines for peripheral IV catheters.

Onset

Immediate vascular access upon successful catheter placement; therapeutic onset depends on the fluids or medications administered.

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