NDL, Gripper Micro, 22G x 0.75″ Blunt Cannula Safety Needle

GRIPPER

Injection & Infusion

Port Access Needles / Safety Cannulae

Manufactured under ISO Certified medical device quality system (ICU Medical).
Latex Free, non Siliconized, DEHP Free materials — suitable for a broad range of patients including those with latex sensitivity.
MR Conditional up to 3 Tesla (when port system is compatible).

Manufactured under ISO Certified medical device quality system (ICU Medical).
Latex Free, non Siliconized, DEHP Free materials — suitable for a broad range of patients including those with latex sensitivity.
MR Conditional up to 3 Tesla (when port system is compatible).

Port Access Needles / Safety Cannulae

Description

Gripper Micro® is a blunt-cannula, non-coring safety needle system designed for accessing implanted ports. The system comprises a sharp trocar inserter and a low-profile infusion site; once the trocar is inserted and removed, a blunt cannula remains in the port for secure, long-term infusion access. The safety arm mechanism locks with an audible “click” when disengaged, and the small cushioned infusion platform improves patient comfort during prolonged therapy. The device is compatible with Taxol and lipid infusions and is intended for single-use only.

Bnefits

Small, low-profile infusion site simplifies dressing and enhances patient comfort during long-term therapy.
Non-sharp blunt cannula reduces risk of needlestick injuries and facilitates safe removal and disposal.
Trocar non-coring needle locks into place for sharps disposal, with audible click confirming safe engagement.
Foam-padded base offers cushioning, improving tolerance during extended infusion sessions.
Compatible with lipid- and Taxol-containing infusions, broadening range of therapeutic applications.
MR-conditional up to 3 Tesla (when port and patient-compatible), advantageous in patients requiring MRI.
Latex-free, non-siliconized, and DEHP-free materials minimize allergic and toxic risks.

Indications

Access of implanted vascular access ports for administration of chemotherapy, lipid-based therapy, fluids or medications.
Long-term infusion therapy requiring secure and comfortable port access.
Use in adult and paediatric patients where a low-profile safety port needle is preferred.

Composition

Cannula: 304 stainless steel blunt cannula (non-coring).
Inserter: Sharp trocar needle (for initial port access) stainless steel.
Base & safety arm: Acrylic copolymer/plastic safety components.
Infusion site pad: Non-absorbent foam pad for patient comfort.
Tubing (when included): PVC, TOTM-plasticized, DEHP-free extension tubing with female luer lock (depending on product variant).

Formulation

Two-piece safety needle and cannula system: sharp trocar for initial port puncture that is removed to leave a blunt cannula for infusion.
Non-coring design prevents damage to port septum, preserving longevity of port access device.
Single-use, sterile, apyrogenic device supplied in sealed packaging.

Packaging

Individual blister (unit pack) containing one Gripper Micro safety needle/cannula set.
Outer cartons typically hold 12 units per box.

Usage

Check the unit packaging for integrity and expiry date before use; do not use if compromised.
Use appropriate aseptic technique when accessing an implanted port, following institutional protocols.
Insert the trocar (sharp needle) into the port; once access is established, remove the trocar so that the blunt cannula remains in place for infusion.
Connect infusion line to the luer lock (if extension set/tubing is included) and secure dressing over the low-profile infusion site.
After infusion therapy is complete, engage the safety arm until it clicks to lock the trocar for disposal safely; dispose of sharps according to local protocols.
Do not reuse; intended for single-use only.

Contraindications

Do not use if the sterile packaging is damaged or the expiry date has passed.
Not for use in non-implanted vascular access or peripheral IV unless device is specifically indicated for that purpose (device is intended for port access).
Do not use if patient has a known allergy to any material in the device (e.g. stainless steel, plastics used).

Adverse Effects

Risk of infection if aseptic technique is not strictly observed during insertion or maintenance.
Local discomfort, irritation or skin reaction at insertion site due to pressure or movement under the dressing.
Potential for port septum damage if non-coring technique fails (rare, when used incorrectly).
Risk of leakage, occlusion or infusion line complications if connections are not secured properly (standard for port access devices).

Storage Conditions

Store in original sealed packaging in a cool, dry place, protected from light and excessive heat or moisture.
Do not use if packaging is damaged or sterility is compromised.

Duration

Used for the duration of each infusion session; the blunt cannula may remain in place for long-term port-access therapy according to clinical protocol and manufacturer\u2019s instructions.