Hybrid implantable ports
Polysite
Description
Designed with the patient and clinician in mind, the Polysite® Low Profile Hybrid Port is available in 6 Fr. Micro, 7 Fr. Mini and 8 Fr… Read more
Indication
The POLYSITE® PI Implantable Infusion Port is indicated for long term access to the central venous system and allows for repeated vascular access. POLYSITE® PI Implantable Infusion Ports are used to administer chemotherapy, antibiotics and antiviral drugs. They can also be used for parenteral nutrition, transfusion of blood or blood products.
POLYSITE® PI Implantable Infusion Ports can be used for high pressure injection of contrast media during diagnostic studies. The maximum flow rate of power injector equipment used with the pressure injectable port may not exceed 5 ml/sec (300psi). For high pressure injection of contrast media, a high-pressure non-coring needle must be used to access the POLYSITE® PI implanted port. The manufacturer recommends the use of PPS PI® pressure injectable safety non-coring Huber needle.
Product highlights
Light and Profile-shaped design:
Polysite® consists of a titanium reservoir and an outer shell made of polyoxymethylene (POM), making Polysite® a lightweight implantable chamber.
All components of Polysite® are radiopaque.
In addition, Polysite® has smooth edges, and its contoured design requires only a small surgical pocket.
The titanium reservoir is resistant to Huber needle punctures.
Pressure injectable
Polysite® is compatible with pressure injection of contrast media during CT scan or MRI procedures up to flowrate 5 ml/s and maximum pressure 325 psi.
Adaptability
Polysite® ports comes in a range of sizes to suit all patient morphologies, from paediatric to adult:
- 3 case sizes (micro, mini, standard). Ports pre-connected or to be connected.
- Different catheter diameters from 5Fr to 10Fr. as well as different lengths (60 to 80 cm). Catheters available in polyurethane or silicone.
The Polysite® range is also designed to suit the needs of every user, with different kits available: surgical, percutaneous and percutaneous with ultrasound-guided puncture.
The implantable ports Polysite® is a Class III sterile medical device. Certification established by GMED notified body no. 0459.
They allow repeated and prolonged access to the venous system.
Read the instructions for use carefully.
Device manufactured by PEROUSE MEDICAL and distributed by VYGON.
Description
Designed with the patient and clinician in mind, the Polysite® Low Profile Hybrid Port is available in 6 Fr. Micro, 7 Fr. Mini and 8 Fr. standard sizes. The hybrid design with durable titanium reservoir and lightweight plastic body provides the strength and comfort needed for long-term treatment in patients of all sizes.
- Port combines lightweight plastic body for comfort and a durable titanium reservoir for durability
- Pressure injectable up to 5 mL/sec at 300 psi*
- Silicone-filled suture holes available for easy explantation
- High flow rates
References and Features
| Implantable port | Catheter | Reservoir | Packaging | |||||
|---|---|---|---|---|---|---|---|---|
| Favourites | Code | Material | Material | Ext. Ø Fr | Volume ml | Volume ml | Units/Box | Units/Case |
| 4018PI | Titanium / POM | Polyurethane | 8 | 0.23 | 0.55 | 1 | 1 | |
Additional information
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Contains Latex No
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Contains animal product No
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Pyrogen-free Yes
Documentation
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EN_Catheter Connection - Polysite
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Instructions for use
