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TITAN-PORT Systems (Arterial/Venous) are fully implantable port systems consisting of an injection chamber (port) a screw closure mechanism, a self-sealing membrane, and a catheter. Each system includes a special puncture needle, this instruction guide, and a patient ID-card. Suitable introducer sets are available seperatly.

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 3000 times 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 PU- (Polyurthane) Catheters.

Only special non-coring port-needles (SFN®-port needles recommended) should be used for puncture of the port membrane. These needles exhibit a unique bevel at the tip. This prevents punch defects of the membrane when the needle is advanced. (22 G or 20 G are recommended). Each system contains a suitable needle.

The TITAN-PORT Systems are MR conditional.

MR Symbol


hochdruck gbAppropriate for Power Injection of contrast media via implanted Portcathetersystems


 Standard sets
 Art.Nr. Port Catheter PZN
  Material Base Height Septum Ø Weight Reservoir Material OD ID Lenght French  
hochdruck d111248 V (venous) 28 mm 12,9 mm 12 mm <16g 0,9 ml Silicone 2,5 mm 1,2 mm 700 mm 7,5 01673250
hochdruck d111248 V-PU (venous) Titanium 28 mm 12,9 mm 12 mm <16g 0,9 ml Polyurethane 2,5 mm 1,2 mm 720 mm 7,5 01673600

Suitable introducer sets are available separately.


Complete setS
 Art.Nr. Port Catheter PZN
  Material Base Height Septum Ø Weight Reservoir Material OD ID Length French  
hochdruck d111248 V-Set (venous)* Titanium 28 mm 12,9 mm 12 mm <16g 0,9 ml Silicone 2,5 mm 1,2 mm 700 mm 7,5 00200762
hochdruck d111248 V-PU-Set (venous)* Titanium 28 mm 12,9 mm 12 mm <16g 0,9 ml Polyurethane 2,5 mm 1,2 mm 720 mm 7,5 00201626
hochdruck d111257 V-PU-Set (venous)* Titanium 28 mm 12,9 mm 12 mm <16g 0,9 ml Polyurethane 3,0 mm 1,2 mm 700 mm 9,0 00205096

*includes introducer and tunnelizer.

hochdruck dAppropriate to high pressure radio-paque material injection - 300 psi/21 bar to 5,2 ml/sec
Power Injection of contrast media via implanted Portcathetersystems


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

In addition some systems may be used for following indications:


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


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


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

To achieve greater flow rates the port membrane may be accessed simultaneously with up to three needles.

(The above mentioned concentrations are recommendations and must always be adapted to patient's coagluation status as monitored by a physician. The product description of all pharmaceuticals used should always be consulted.)


CAUTION: High-pressure injections not unless patency of the system is confirmed by the physician (aspiration, manual
injection). In case of any doubt injection should be avoided!

Causes of abnormally high resistance to access needle may include

Blood deposits in the system generally indicate one of the following causes:


INDICATIONS FOR EXPLANTATION


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.


CARE OF THE SYSTEM AND SPECIAL RECOMMENDATION

Before each access the correct position of the portal chamber must be checked by palpation. Any signs of infection must be excluded. Without complications the TITAN-PORT Systems can be used one day after implantation.

Palpation Port

 


Accessories for Seldinger Technique
Art.-Nr. Descrition PZN
ITS 432008 F Introducer 8 F, peel-away 02259794
ITS 432009 F Introducer 9 F, peel-away 02259848


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