Abbott Laboratories Vascular Enterprises Limited

Coremedic Ag

Invatec Technology Center Gmbh

Medtronic, Inc.

Sulzer Orthopedics Inc.

Universitât Bern

Acotec Scientific Co. Ltd

Schaffner Silvio

Invatec S.p.a

Invatec S.r.l.

Coremedic Gmbh

Silvio Schaffner

Marc Gianotti

Gerd Seibold

Joost J Fierens

Oliver Wüthrich

Tobias Aeschlimann

Thomas Bauer

Randolf Von Oepen

Ulrich Speck

Andrea Guidotti

Andrea Venturelli

Albert Maria Vodermayer

David Zarbatany

Magdalena Renke-Gluszko

Jens K&auml;rger

Hans Erlach

Armin Studer

Thierry Carrel

Georgios Stefopoulos

Andreas Mächler

Stijn Vandenberghe

Alberto Weber

Jesus Flores

Louis Weidmann

Gudrun Grimberg

Rolf Vogel

Stefan Guggisberg

Venturelli Andrea

Michael Roth

Oliver WÜTHRICH

Andreas MÄCHLER

Tommaso Sironi

Luca Vicentini

Mattia Arduini

A sutureless implant for replacing damaged natural chordae tendineae of a human or possibly animal heart, the implant including a distal implant part, a proximal implant part, and an artificial chord. The distal implant part is configured to fit in a lumen of an implant delivery device and includes a self-spreading portion spreading radially outside when the distal implant part is released from the lumen, the self-spreading portion being capable of anchoring the distal implant part in human muscle tissue. The proximal implant part is configured to fit in the lumen of the implant delivery device and comprises a self-spreading portion spreading radially outside when the proximal implant part is released from the lumen, the self-spreading portion being capable of bearing on a tissue portion of leaflet tissue. The distal implant part and the proximal implant part are connected by the chord.

Medical implant and method for heart valve repair

An instrument for repairing an atrioventricular heart valve, the instrument including a tubular element having an outer, distal end; a distal implant part arranged in the tubular element; an artificial chord arranged in the tubular element; a proximal implant part arranged in the tubular element; and, an anchor carrier arranged in the tubular element. The distal implant part and the proximal implant part are arranged in the tubular element beside one another, with the distal implant part being closer to the distal end of the tubular element than the proximal implant part The proximal implant part is assembled with the anchor carrier inside the tubular element so that the tubular element prevents the proximal implant part from escaping from the anchor carrier as long as the anchor carrier is within the tubular element.

Medical apparatus and method for heart valve repair

The present invention relates to a drug-eluting medical device, in particular a balloon for angioplasty catheters with drug elution to prevent the restenosis of the vessel subjected to angioplasty. More particularly, the present invention relates to a catheter balloon completely or partially coated with paclitaxel in hydrated crystalline form or in hydrated solvated crystalline form, having an immediate release and bioavailability of a therapeutically effective amount of paclitaxel at the site of intervention. The balloon can be made of a polyether-polyamide block copolymer, or a polyester amide, or polyamide-12.

Drug-eluting medical device

A sutureless implant for replacing damaged natural chordae tedingeae of a human or possibly animal heart, the implant including a distal implant part, a proximal implant part, and an artificial chord. The distal implant part is configured to fit in a lumen of an implant delivery device and includes a self-spreading portion spreading radially outside when the distal implant part is released from the lumen, the self-spreading portion being capable of anchoring the distal implant part in human muscle tissue. The proximal implant part is configured to fit in the lumen of the implant delivery device and comprises a self-spreading portion spreading radially outside when the proximal implant part is released from the lumen, the self-spreading portion being capable of bearing on a tissue portion of leaflet tissue. The distal implant part and the proximal implant part are connected by the chord.

A surgical instrument implementing a leaflet grabbing mechanism by a leaflet grabbing structure, in which the leaflet can be grabbed and clamped between first and second abutment surfaces. The first, proximally facing abutment surface belongs to a swivel-out portion of the leaflet grabbing structure, which includes at least a first arm and a second arm. In a released state, when the leaflet grabbing structure is released from a catheter, the arms are capable of swiveling: the first arm may swivel with respect to a main body to which it is attached, and the second arm may swivel relative to the first arm so that in a leaflet grabbing position the first abutment surface faces proximally. The second arm includes a recess arranged so that a chord extending between a released distal implant part and a proximal implant part can extend therethrough and be released by a lateral relative movement.

Medical instrument and method for heart valve repair

Apparatus and methods for stenting are provided comprising a stent attached to a porous biocompatible material that is permeable to endothelial cell ingrowth, but impermeable to release of emboli of predetermined size. Preferred stent designs are provided, as well as preferred manufacturing techniques. Apparatus and methods are also provided for use at a vessel branching. Moreover, embodiments of the present invention may comprise a coating configured for localized delivery of therapeutic agents. Embodiments of the present invention are expected to provide enhanced embolic protection, improved force distribution, and improved recrossability, while reducing a risk of restenosis and thrombus formation.

Methods and apparatus for stenting comprising enhanced embolic protection coupled with improved protections against restenosis and thrombus formation

A surgical instrument for treating atrioventricular valve prolapse of the drained human heart, includes a handle for being held by a surgeon, a shaft extending distally from the handle, the shaft having a lumen open to a shaft distal end, a cannulated needle arranged in the shaft; with a distal end of the needle protruding from the shaft distal end at least in one possible needle position. The needle accommodates a first, distal implant equipped for being anchored in a papillary muscle, and a second, proximal implant shaped to hold on to a leaflet of an atrioventricular valve, the first and second implants each including a chord connector portion for connecting the respective implant to an artificial chord. The apparatus further includes a trigger arrangement for releasing the first, distal implant upon a first release actuation and for releasing the second, proximal implant upon a second release actuation.

Catheters and methods of making catheters are provided which include a connector with a guide wire channel and an inflation channel, a shaft extending from a proximal end to a distal end and having a guide wire lumen and an inflation lumen, the shaft being connected, at its proximal end, to the connector so that said guidewire lumen and inflation lumen are mechanically and fluidly connected with said guide wire channel and inflation channel respectively. The connection is realized in correspondence to a kink portion. Such catheters may include a protective sheath placed around an external wall of the shaft extending from a first sheath end, axially placed at a first distance from the proximal end of the shaft so as to allow direct contact and fixation between the external wall of the shaft and the internal wall of the kink portion, to a second sheath end.

Catheter assemblies having a protective sheath and methods of manufacture

The present invention relates to an endolumenal prosthesis comprising a tubular body adapted to convert from a contracted condition to an expanded condition. The tubular body develops along a longitudinal axis and comprises: a plurality of coils and at least one bridge. The coils develop along a substantially circumferential direction and the bridge connects two coils. The coils are realized in a persistent material, while the bridge is realized in a bioabsorbable material.

Endolumenal prosthesis

Growing community of inventors

Berlingen, Switzerland

Silvio Schaffner