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   PM 52klgport label


 

TITAN-PORT G

 Port puncture with all needles!  

Advantages compared to standard port catheter systems: 

PakuMed Port GKat GW 5991

 

TITAN-PORT G is a totally implantable port catheter system consisting of an injection chamber (port), a screw closure machanism, a self-sealing silicone membrane and a catheter. Each system includes aspecial access needle, a dilatator, catheter introducer, these instructions for use and a patient ID-card. Some sets contain introduction instruments and tunnelizers.

The port chamber consists of hypoallergenic biocompatible titanium. This material is non-magnetic. The base plate has openings for securing the system with sutures to the fascia. The port chamber and the catheter can be disconnected.

The silicone membrane can be punctured up to 3000x with the enclosed non-coring special puncture needle. The membrane possesses a high-pressure stability and ensures proper positioning of the needle when placed.

The catheter (various models, sizes and materials depending on indication) can be shortened to the individual length required. It bears radiopaque calibration markings at 5 cm intervals, and is conically tapered at the tip. The arterial catheter has three distal fixation rings. The same applies to PUR (Polyurthane) Catheters.

The patient ID card is filled out by the doctor who performed the implantation and is given to the patients who should always carry this document with them.

The instructions for use should also be available to nurses and doctors responsible for follow-up care.

MR conditional

TITAN-PORT catheter systems are MR-conditioned-safe. On request, we will be happy to provide you with further information.


 

 

 

 G Port One for All

 

 

 


INDICATIONS
The TITAN-PORT-Systems ensure repeated access to the vascular system for the following indications:.


CONTRAINDICATIONS
The TITAN-PORT systems should not be used in:


COMPLICATIONS and potential ADVERSE REACTIONS
UThe following complications or adverse reactions can occur:


INSTRUCTIONS FOR USE / PORT IMPLANTATION
Caution: During implantation sterile handling is absolutely mandatory!

The choice depends on the surgeon's preference

If the situation is unclear or thrombotic obstruction is suspected a radiographic or Doppler sonographic control is necessary. To achieve greater flow rates the port membrane may be accessed simultaneously with up to three needles.


CAUTION
Causes of abnormally high resistance to access needle may include

Blood deposits in the system generally indicate faulty handling, leakage or a defective septum inside the port.
When blood aspiration is not successful, the port should be flushed and the patient's position changed.


INDICATIONS FOR EXPLANTATION

The port can be removed under local anesthesia at the end of treatment. Other indications include:


WARNINGS


PRECAUTIONS
Sterility

Meticulous hygiene and sterile handling technique are mandatory for the safe usage of TITAN-PORT Systems.This includes:


AFTERCARE AND MONITORING

Regular treatment sessions and associated care of the port system are coincidental with monitoring of the port system.
Port systems should not be used by physicians / health care personnel not familiar with all aspects of the product and its potential complications. Complications can occur at any time during and after implantation.


 Art.Nr. Port Catheter     PZN
  Material Base Height
Septum Ø Weight
Material OD ID Length French  
111248 G-SET* Titanium 28 mm 13,4 mm 12 mm <16 g Silicone 2,5 mm 1,2 mm 700 mm 7,5 06149298

*including introducer set and tunnelizer