PakuMed Port MittelKat GW 5965 PakuMed Port Mittel GW 5300 PakuMed Katheter GW 5785 PakuMed Umverpackung GW 5932 PakuMedSML02

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

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

The silicone membrane can be punctured frequently (up to 3000 times) with a suitable special needle, e.g. the enclosed SFN non-coring access needle. The membrane is highly resistant to pressure and holds the inserted needle reliably in place.

The catheter (various models, sizes and materials - depending on indication) can be shortened proximally to the individual length required. It bears calibration markings at 5 cm length intervals and is conically tapered at the tip. It has an additional opening at the side (especially to facilitate blood sampling). The arterial catheter has two additional distal fixation rings.

Introduction instruments include a puncture needle, a guide wire, and a dilatator which facilitate introduction of catheters into the blood vessels via Seldinger's technique. The tunnelizer aids in passing the catheter through the subcutaneous tissues.

Only special non-coring port needles (e.g. SFN portneedles) should be used to puncture the port membrane. The needles exhibit a unique bevel and angle at the tip. This prevents punch defects of the membrane when the needle is inserted. Different lengths and diameters are available. 22G or 20G is recommended for standard use. Each system contains a suitable needle.

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:

hochdruck gbAppropriate for Power Injection of contrast media via implanted Portcathetersystems

MR conditional

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

 Standard sets
 Art.Nr. Port Catheter PZN
  Material Base Height Septum Ø Weight Reservoir Material OD ID Lenght French  
hochdruck d111246 V (venous) Titanium 25 mm 12,7 mm 12 mm <12g 0,6 ml Silicone 2,5 mm 1,2 mm 700 mm 7,5 01673221
hochdruck d111246 V-PU (venous) Titanium 25 mm 12,7 mm 12 mm <12g 0,6 ml Polyurethane 2,5 mm 1,2 mm 720 mm 7,5 01673238

Suitable introducer sets are available separately.

CompletE sets
 Art.Nr. Port Catheter PZN
  Material Base Height Septum Ø Weight Reservoir Material OD ID Lenght French  
hochdruck d111246 V-Set (venous)* Titanium 25 mm 12,7 mm 12 mm <12g 0,6 ml Silicone 2,5 mm 1,2 mm 700 mm 7,5 00200733
hochdruck d111246 V-PU-Set (venous)* Titanium 25 mm 12,7 mm 12 mm <12g 0,6 ml Polyurethane 2,5 mm 1,2 mm 720 mm 7,5 00200756

*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

The TITAN-PORT Systems ensure repeated access to the vascular system for example for the following indications:infusion therapy and long-term

In addition some systems may be used for following indications:

The TITAN-PORT systems should not be used in:

The following complications or adverse reactions can occur:

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:




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


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.


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

info ports5 big
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