PRODUCT INFORMATION

Notice: The MaRVis MR Guidewires are not yet cleared for sale or use in the U.S.

All MaRVis MR Guidewire products as presented below are CE certified for human use only in Europe.

The MaRVis MR Guidewires are intended for use in MRI-guided interventional medical procedures to reach the target region in the human body and/or to advance catheters or catheter-based instruments over the guidewire.

The MaRVis MR Guidewires must be used by a well-trained physician.



General technical features
CoreMonobloc design
Base materialFiber-reinforced plastics rods (glass and aramid) 
SurfacePTFE shrink tube
Flexible tip

Straight, manually shapeable

MRI visibility          
Continuous line along the entire length; additional ball-shaped tip marker
X-ray visibilityAlong the flexible tip
MR safety"MR Safe"



The MaRVis Amber Wire product line is CE marked for use in intraluminal interventions in natural body orifices in the urinary tract, the genital tract or the gastrointestinal tract and in non-vascular interventions in the trunk and the limbs.

The MaRVis Amber Wire is not intended for application in the peripheral or central circulatory system.

The guidewire variants are:

MaRVis Amber Wire
DiameterTypeTipLength
0.035"standardType A150, 180, 210, 260, 300 cm
0.035"stiffType A150, 180, 210, 260, 300 cm
0.035"stiffType B60, 180 cm
0.014"microType A190, 250, 300 cm



The MaRVis Sunglow Wire product line is CE marked for use in endovascular interventions in the peripheral and central circulatory system. The MaRVis Sunglow Wire is not intended for application in the cerebrovasculature.

The guidewire variants are:

MaRVis Sunglow Wire
DiameterTypeTipLength
0.035"standardType A150, 180, 210, 260, 300 cm
0.035"stiffType A150, 180, 210, 260, 300 cm
0.014"microType A190, 250, 300 cm

 


For availability please contact MaRVis.

 

Download of Instructions for use

 

Access to Eudamed databank: ec.europa.eu/tools/eudamed/

MaRVis Interventional GmbH

print