Inflow Dynamics, Inc.

Dr. Ruhland Nachf. Gmbh

Stemberger, Axel

Schmidmaier, Gerhard

Raschke, Michael

Axel Stemberger

Eckhard U Alt

Thilo Fliedner

Gerhard Schmidmaier

Michael Raschke

Robert Alter

A vascular or endoluminal stent adapted for deployment in a vessel or tract of a patient to maintain an open lumen therein is formed from a metal open-ended tube which is the single component of the stent. The tube has a multiplicity of holes cut by laser through its wall. The through-holes are encompassed by serpentines that constitute the wall, the serpentines extending sinusoidally each in multiple 360.degree. wavelengths in a single turn about the axis of the tube and juxtaposed in plural substantially identical segments disposed with regularity along the axis. Each segment has a length equal to the distance between crests and troughs of the sinusoid. Adjacent serpentines are joined together at crest and trough, respectively, so that their interconnections are 180.degree. out of phase relative to their wavelength. The serpentines and interconnections thereof are shaped throughout for optimum uniform expansion of the stent during deployment thereof including a notch substantially symmetrically located at either side of the junction of the respective crest and trough of the interconnections between adjacent serpentines. The serpentines are substantially devoid of sharp corners and edges, except at the notches, and each serpentine has an oval cross-section. The regularity of the segments is interrupted at least once along the axis of the tube by serpentines oriented differently from the others, used to maintain the tube's length substantially invariant despite radial expansion of the stent during deployment. The serpentines are pre-stressed and annealed before deployment of the stent to ease deployment and enhance symmetrical radial expansion. The exterior surface of the tube is longitudinally tapered from its mid-point toward its ends, and substantially rounded surfaces prevail throughout the tube.

Implantable vascular and endoluminal stents

A vascular or endoluminal stent adapted for deployment in a vessel or tract of a patient to maintain an open lumen therein is formed from a metal open-ended tube which is the single component of the stent. The tube has a multiplicity of holes cut by laser through its wall. The through-holes are encompassed by serpentines that constitute the wall, the serpentines extending sinusoidally each in multiple 360.degree. wavelengths in a single turn about the axis of the tube and juxtaposed in plural substantially identical segments disposed with regularity along the axis. Each segment has a length equal to the distance between crests and troughs of the sinusoid. Adjacent serpentines are joined together at crest and trough, respectively, so that their interconnections are 180.degree. out of phase relative to their wavelength. The serpentines and interconnections thereof are shaped throughout for optimum uniform expansion of the stent during deployment thereof, including a notch substantially symmetrically located at either side of the junction of the respective crest and trough of the interconnections between adjacent serpentines. The serpentines are substantially devoid of sharp corners and edges, except at the notches, and each serpentine has an oval cross-section. The regularity of the segments is interrupted at least once along the axis of the tube by serpentines oriented differently from the others, used to maintain the tube's length substantially invariant despite radial expansion of the stent during deployment. The serpentines are pre-stressed and annealed before deployment of the stent to ease deployment and enhance symmetrical radial expansion. The exterior surface of the tube is longitudinally tapered from its mid-point toward its ends, and substantially rounded surfaces prevail throughout the tube.

Implantable vascular and endoluminal stents and process of fabricating

A method is disclosed for coating a biomaterial to be placed in contact with a patient's blood flow to inhibit blood coagulation from adhering to the biomaterial that would otherwise result from such contact. A biodegradable material of liquid state compatible with the blood and tissue of the human body is prepared, and an anti-coagulant drug is incorporated into the liquid state of the biodegradable material to form a liquid coating material. The liquid coating material is adhesively applied to a surface of the biomaterial in a substantially continuous overlying layer having a formulation, pattern and thickness selected according to the period of time over which the coating material is to perform its anti-coagulant action. Thereafter the coating material is dried to a layer thickness less than about 100 microns for continuous disintegration thereof as a function of time when the layer is in contact with flowing blood. The method is utilized in an exemplary embodiment in which the biomaterial is a vascular stent.

Biodegradable coating with inhibitory properties for application to

A collagenous dressing which is characterized in that it contains collagen in combination with a resorbable biopolymer from the group comprising fibrinogen, gelatin modified by SH groups, collagen modified by SH groups, or regenerated oxycellulose modified by SH groups. Said collagenous dressing is tissue-agglutinable and does not have the disadvantages of conventional fibrin bonding in combination with resorbable collagen.

Growing community of inventors

Neubiberg, Germany

Axel Stemberger