Gastric ring with membranous bridge
AssigneeCompagnie Europeene d'Etude et de Recherche de Dispositifs pour I'lmplantation par Laparoscopie
InventorJean-Paul Ricol
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Abstract
The invention relates to an implantable surgical ring (1) intended to close on itself around a mean extension axis in order to enable adjustment of the section through which a biological organ passes, said ring being characterized in that the same comprises at least one first and one second gripping bag (10, 11) that are tiered along the mean extension axis, are designed to be filled with filling fluid, and respectively have a first peak portion (12) and a second peak portion (13), and in that said first and second peak portions (12, 13) are separated by a separation area (14) including a retaining means (20) receding away from said first and second peak portions (12, 13) to limit the depth (P) to which the gripped biological organ can enter between said first and second peak portion.
Claims14
Implantable surgical ring designed to be closed on itself in order to form a closed loop around a mean axis of extension so that it can grip a biological organ constituting a pocket or a duct in order to modify the section of passage of said biological organ, said ring comprising at least one first gripping pocket and one second gripping pocket which are tiered relative to each other along the mean axis of extension and designed to be filled with a filler fluid so as to provide for the gripping of the biological organ, said first and second gripping pockets respectively having a first peak portion and a second peak portion which project towards the interior of the loop to push against said biological organ, and said first and second peak portions are separated from each other by a separation zone which defines a matter-free clearance zone sufficiently marked to provide for a discontinuity of contact between the biological organ and the surgical ring, between the peak portions, and which comprises a retaining means receding away from said first and second peak portions and designed to limit the penetration depth at which the gripped biological organ is liable to penetrate between said first and second peak portions so as to prevent damage to the wall of the biological organ in the separation zone.
Dependencies are inferred from the claim text.