INTERLINK Needle Free Injection Site

Interlink

Medical device

Needle-free IV injection site / connector

CE Marked as a sterile, single Use IV accessory under applicable EU/UK medical device regulations.
Manufactured under an ISO 13485 Compliant quality management system (typical for Baxter IV devices).
Non DEHP, non PVC and latex Free construction in line with current safety standards for IV accessories.

CE Marked as a sterile, single Use IV accessory under applicable EU/UK medical device regulations.
Manufactured under an ISO 13485 Compliant quality management system (typical for Baxter IV devices).
Non DEHP, non PVC and latex Free construction in line with current safety standards for IV accessories.

Needle-free IV injection site / connector

Description

The INTERLINK Needle-free Injection Site is a sterile, single-use IV injection port designed to provide needleless access to an intravenous line. Featuring a male luer lock adapter and a split-septum needle-free connector, it enables clinicians to inject or withdraw fluids using standard luer devices without the use of hypodermic needles, helping to reduce needlestick injuries and maintain a closed IV system. The connector is non-DEHP, non-PVC and latex-free, and is supplied individually sterile, commonly in cases of 200 units for clinical use. This Medisave listing is a clearance item due to a short expiry date (October 2023).

Bnefits

Needle-free IV access, reducing the risk of needlestick injuries to healthcare staff.
Maintains a closed IV system, helping to minimise contamination and infection risk.
Male luer lock adapter provides secure connection to compatible IV lines and devices.
Negative-displacement, split-septum design (Interlink system) supports effective flushing and reduces occlusion risk.
Non-DEHP, non-PVC and latex-free construction suitable for sensitive patients.
Supplied sterile and ready to use, simplifying IV line setup.
Compatible with Interlink IV systems and standard luer-tipped syringes and accessories.

Indications

Needle-free access to an existing intravenous line for intermittent injections or medication administration.
Use as an injection site on IV administration sets, extension sets or catheter hubs.
Situations where reducing needlestick injury risk and maintaining a closed IV system are required.
General hospital, clinic, emergency and outpatient IV therapy settings.

Composition

Housing and adapter: medical-grade plastic, non-DEHP and non-PVC.
Septum: elastomeric material (such as silicone or similar medical-grade elastomer) forming a split-septum needle-free valve.
Connector: male luer-lock fitting compatible with standard female luer devices.
Packaging: individual sterile barrier pouch for each connector.

Formulation

Device type: needle-free IV injection site / needleless connector.
Connection type: male luer-lock adapter.
Valve type: split-septum, negative-displacement needle-free connector designed for Interlink systems.
Intended use: single-patient, single-use sterile IV accessory.

Packaging

Individually packaged in sterile, peel-open pouches.
Typical case configuration: 200 needle-free injection sites per case (may vary by distributor).
Medisave clearance listing supplied as individual units from original cases (short expiry stock: October 2023).
Labelling includes product name, brand (Interlink), manufacturer (Baxter), lot number and expiry date.

Usage

Inspect the sterile pouch prior to use; do not use if packaging is opened, damaged or past the expiry date.
Using aseptic technique, remove the injection site from its packaging.
Connect the male luer-lock adapter securely to the compatible IV line or device according to local protocol.
Disinfect the needle-free septum with an appropriate antiseptic swab and allow to dry before each access.
Attach a standard luer-locked syringe or compatible IV device to the connector; inject or withdraw fluids as prescribed.
After use, flush the connector and IV line as per institutional guidelines to maintain patency.
Replace the connector according to local policy, or sooner if contamination, damage or malfunction is suspected.
Dispose of the used device as clinical waste in accordance with local regulations; do not reuse or re-sterilise.

Contraindications

Do not use if the sterile package is damaged, opened or if the product is expired.
Not intended for arterial lines or applications outside standard IV therapy unless specifically indicated by the manufacturer and local protocols.
Do not use with non-luer compatible devices.
Do not use in patients with known hypersensitivity to any of the device materials, although the product is latex-free and non-DEHP.
Do not reuse or re-sterilise; single-use only.

Adverse Effects

Potential increased risk of infection if aseptic technique is not strictly followed during use and access.
Possible leakage or disconnection if the luer-lock is not properly secured.
Risk of occlusion, thrombus formation or inadequate flow if device is not properly flushed or maintained.
In rare cases, local irritation or hypersensitivity reactions to device materials.

Storage Conditions

Store in a clean, dry environment at room temperature.
Keep away from excessive heat, cold, moisture and direct sunlight.
Maintain in original packaging until immediately prior to use to preserve sterility.
Do not use beyond the expiry date printed on the packaging.

Duration

Not applicable; used for the duration of IV therapy or according to local line-change policies, but designed as a single-use sterile device per patient/line episode.