PakuMed medical products gmbh of Essen at MEDICA 2021 in Düsseldorf -- MEDICA - World Forum for Medicine
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PakuMed medical products gmbh

Im Löwental 79, 45239 Essen
Germany
Telephone +49 201 437097-0
Fax +49 201 437097-29
info@pakumed.de

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Hall map

MEDICA 2021 hall map (Hall 7a): stand F05

Fairground map

MEDICA 2021 fairground map: Hall 7a

Our range of products

Product categories

  • 01  Imaging and diagnostics / medical equipment and devices
  • 01.05  Implants and protheses
  • 01.05.04  Other implants and protheses

Our products

Product category: Other implants and protheses

TITANIUM PORTS MEDIUM

TheTITAN-PORTsystems are fully implantable port catheter systems. They consist of an injection chamber (port) with a twist-lock mechanism and a self-sealing silicone membrane, and a catheter. Each system also includes a special puncture cannula, a refill cannula, a venous hook, these instructions for use and a patient passport, and in some cases also a matching introducer set and a tunnelizer.

Theport housingis made of hypoallergenic, biocompatible titanium. The material has no magnetic properties. There are suture holes in the base plate to fix the system to the muscle fascia. Port housing and catheter are deconnectable.

Thesilicone membrane can be punctured many times (up to 3000 times) with a suitable special cannula, e.g. the enclosed SFN® non coring needle. It is characterized by high pressure stability. The membrane holds the needle in position.

Thecatheter(different designs, sizes and materials depending on the application) can be shortened proximally individually to the required length. It is graduated every 5 cm, the tip is tapered and there is an additional hole on the side (mainly for improved blood sampling). The respective catheter (silicone or polyurethane) is radiopaque, the arterial catheter is additionally provided with two fixation rings distally. The introducer set contains a puncture cannula, the guide wire and a dilator and is used to place the catheter in the blood vessel, e.g. using the seldinger technique.

Thetunnelizeris used for subcutaneous guidance and placement of the catheter, if necessary. For the puncture of the membrane, only non-coring special needles (e.g.SFN® port needles or other suitable port needles) with a special cut (different diameters and puncture lengths are available) may be used. Recommended for standard use are 22 or 20 gauge cannulas. This avoids punching out a puncture channel or silicone particle when puncturing the membrane. An appropriate cannula is included with each system.

Thepatient passportis filled out completely by the implanting physician and given to the patient, who should always carry the passport with him/her.

Theinstructions for useshould also be available to the doctor providing further treatment and to the nursing staff. The product-specific data and article numbers can be found in the catalogue. The contents of the product are noted on the label of the double-sterile individual packaging. The port catheter system isMRI compatible.

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Product category: Other implants and protheses

TITAN-PORT D (DIALYSIS - SINGLE/DOUBLE LUMEN)

TITAN-PORT D (dialysis) is a fully implantable PORT system made of titanium as an access option for performing veno-venous dialysis. Depending on the product, the set includes one or two suitable port chambers with self-sealing silicone membrane and the respective matching port catheter, screws for fixation. Each system is also supplied with suitable special puncture cannulas, insertion instruments, tunnelizer, instructions for use and patient passport.

Theport housings(chambers) are each made of hypoallergenic, biocompatible titanium. The material has no magnetic properties. The chamber has the following dimensions: width 24 mm, length 36 mm, height 17.5 mm, weight 25 g and internal volume 0.6 ml, an outflow tube of diameter 3.5 mm. There are two suture holes in the base plate for fixing the system to the muscle fascia. The port housing and the catheter can each be deconnected and are connected to each other by means of a twist-screw mechanism with a sleeve via the outflow tube.

Thesilicone membranein the port can be punctured many times (up to 1000 times) with the corresponding punch-free special puncture cannula. It is characterized by high pressure stability. The membrane holds the needle in position.

There are2 different systems available withdouble-lumen PU catheter 14 F andsingle-lumen silicone catheter 12 French.

Thedouble-lumen PU catheter 14 F has two openings at the distal end corresponding to the internal divided course, also recognizable by the respective marking. The longer leg is used for blood outflow, the posterior opening with two additional lateral holes is used for blood inflow. The inner volume of the longer leg is 2.3 ml, of the shorter leg 2.2 ml. Due to the distance between the openings and the natural direction of blood flow of venous blood to the central blood vessels, mixing of blood is minimized and irrelevant for the effect of "blood washing". The inflow and outflow legs of the catheter are connected accordingly to the two implanted ports. These legs can also be shortened if necessary.

Thesingle-lumen silicone catheter 12 F with an outer diameter of 4.0 mm, an inner diameter of 2.5 mm, a total length of 40 cm and an inner volume of 1.6 ml, has 6 side holes at the distal end, a round shaped tip and can also be shortened at the proximal (non-perforated) end if required. The distal round tip prevents flotation of the catheter tip at the dwelling site after implantation, e.g. due to suction or pulsation in the blood vessel, and reduces adhesion to the vessel wall, which also improves the flow rate.

Only the associated special puncture cannulas may be used for puncturing the membranes!

In order to achieve the blood flow rate required for dialysis purposes, appropriately large-volume cannulas are required, e.g. DPK 1835 and DPK 2035. These are characterized by a special grinding to prevent fragmentation of silicone particles and punching of a puncture channel in the membrane. Suitable cannulas are included with each system. These are available separately for further applications.

The enclosedpatient passportis filled out completely by the implanting physician and given to the patient, who should always carry the passport with him/her.

The instructions for use should also be available to the doctor providing further treatment and to the nursing staff.
The contents of the set are indicated on the label of the double-sterile blister pack.

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Product category: Other implants and protheses

TITANIUM PORT APH (EXTRACORPOREAL APHERESIS)

TITAN-PORT APH (extracorporeal apheresis) is a fully implantable PORT system made of titanium as an access device for performing extracorporeal apheresis (examples: photopheresis, lipopheresis, etc.). The set includes a port chamber with a self-sealing silicone membrane and a single-lumen silicone catheter with a connection to the port chamber, a screw to fix the catheter to the outflow tube. Each system also comes with a special puncture cannula, introducer, tunnelizer, instructions for use, and a patient passport.

Theport housing (chamber) is made of hypoallergenic, biocompatible titanium. The material has no magnetic properties. The chamber has the following dimensions: width 24 mm, length 36 mm, height 17.5 mm, weight 22 g and internal volume 0.6 ml, an outflow tube of diameter 3.5 mm. There are two suture holes in the bottom plate for fixation of the system to the muscle fascia. Port housing and catheter are each deconnectable and are connected to each other by a twist and screw mechanism with a sleeve over the outflow tube.

Thesilicone membranein the port can be punctured many times (depending on the diameter) with the corresponding punch-free special puncture cannula. It is characterized by high pressure stability. The membrane holds the needle in position.

Thesingle-lumen silicone catheter 12 F, length 60 cm, has several openings at the distal end and can be shortened if necessary. The internal volume of the uncut catheter is 2.9 ml

Only the corresponding special puncture cannulas may be used for puncturing the membranes!

In order to achieve the blood volume necessary for apheresis, appropriately large-volume cannulas are required, e.g. DPK 1835 and DPK 2035 or SFN 1535 G. These are characterized by a special ground-glass tip. These are characterized by a special grinding to avoid fragmentation of silicone particles as well as the punching out of a puncture channel in the membrane. A corresponding cannula is included with each system. These are available separately for further applications.

The enclosed patient passport is filled out completely by the implanting physician and handed over to the patient, who should always carry the passport with him/her.

The instructions for use should also be available to the doctor providing further treatment and to the nursing staff.
The contents of the set are noted on the label of the double sterile blister packaging.

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About us

Company portrait

Medical technology can be geared to one indication or to all involved. We orient ourselves according to this. First and foremost, of course, the patient is the focus. Especially when it comes to port catheter systems. Port systems are used on a long-term basis, usually for weeks, sometimes even for years. So you not only have to live with the disease, but also with the port.

Therefore, biocompatibility and wearing comfort are top priority. And a robustness that ensures as far as possible that an operation really only has to be performed once.

Doctors need a broad selection, easy implantability and, finally, a port must be easy and safe for the user. For example, thanks to a silicone membrane that is durable and can withstand many punctures. Then there are our special SFN® port cannulas, which function without hooks and eyes. Puncture-free!

We have stood for all this and more since our founding. PakuMed was created by medical professionals, our products are answers. Ideas that should actually be self-evident, but that only we offer. Also because we have developed and expanded our connections to universities, research institutes and users. To buyers, too, of course. Our solutions are economical.

We deliver internationally from our headquarters in Essen.

We are certified according to DIN EN ISO 13485, Annex II.3, II.4 and V of Directive 93/42/EEC