Abstract: A surgical implant adapted for repairing a tissue or muscle wall defect comprises an areal, flexible basic structure which defines a primary region and at least one arm starting from the primary region and having a free end and an end area extending up to the free end. The arm is folded back and fixed (e.g. welded, sutured or glued), in its end area, to the primary region of the basic structure. Preferably, the basic structure is made from one piece and comprises a mesh.

Abstract: A surgical implant (1) adapted for repairing a tissue or muscle wall defect comprises an outer section (8) and an inner section (6) located in the outer section (8), wherein the outer section (8) and the inner section (6) are formed from one double-sheet of a flexible basic structure, which preferably comprises a mesh. The implant can be strengthened by reinforcement elements (12).

Abstract: A surgical implant (1) adapted for repairing a tissue or muscle wall defect comprises an outer section (8) and an inner section (6) located in the outer section (8), wherein the outer section (8) and the inner section (6) are formed from one double-sheet of a flexible basic structure, which preferably comprises a mesh. The implant can be strengthened by reinforcement elements (12).

Abstract: A self-anchoring tissue lifting device for use with facial cosmetic reconstructive surgery includes an implant and a removable foil cover disposed on the implant. The implant includes an elongated mesh strip having a distal end on which is situated a tissue anchoring fleece material. Opposite lateral edges of the mesh material are preferably laser cut during the manufacturing process of the implant to provide a plurality of tissue engaging prickles along the longitudinal length of the implant. For treating the mid face and jowl, a stab incision is made within the hairline of the temple region of the patient and the device is applied from the temporal area to the peak of the ipsilateral cheek to capture the malar fat pad to correct midface abnormalities or the ptotic tissue causing the jowl.

Abstract: A surgical implant (1) adapted for repairing a tissue or muscle wall defect comprises an a real, flexible basic structure which defines a primary region (4) and at least one arm (6) starting from the primary region (4) and having a free end and an end area extending up to the free end. The arm (6) is folded back and fixed (e.g. welded, sutured or glued), in its end area, to the primary region (4) of the basic structure. Preferably, the basic structure (4, 6) is made from one piece and comprises a mesh.

Abstract: A device and method for ligating diseased tissue. The device includes a flexible, substantially tubular sleeve adapted to be positioned around tissue to be ligated and having first and second ends, and at least one anchoring member coupled to the tubular sleeve having an anchoring element positioned substantially adjacent to the first end. The anchoring member has at least one projecting element extending therefrom and adapted to engage healthy tissue when the ligation device is positioned around the tissue to be ligated. The device further includes an elastic element positioned around the periphery of the sleeve and adapted to apply a constrictive force around the periphery of the sleeve.

Abstract: An inhaler for inhaling powdered medicaments from capsules, having: a lower part which is cup-shaped, a plate latched to the lower part to close off the lower part, a capsule holder arranged on the underside of the plate, a mouthpiece that can be latched to the top of plate, and an actuating member for interacting with at least one pin for piercing a capsule in the capsule holder, where the actuating member includes a larger outer actuating member and a smaller inner actuating member, the outer actuating member forms a user-operated push-button, the inner actuating member contacts and holds the pin below a suspension element of the outer actuating member from the plate, and the point of application of force by the user onto push-button is lower than the inner actuating member.

Abstract: A device and method for ligating diseased tissue. The device includes a flexible, substantially tubular sleeve adapted to be positioned around tissue to be ligated and having first and second ends, and at least one anchoring member coupled to the tubular sleeve having an anchoring element positioned substantially adjacent to the first end. The anchoring member has at least one projecting element extending therefrom and adapted to engage healthy tissue when the ligation device is positioned around the tissue to be ligated. The device further includes an elastic element positioned around the periphery of the sleeve and adapted to apply a constrictive force around the periphery of the sleeve.

Abstract: A process for producing a container comprising an outer container, an inner bag disposed therein and a pressure equalisation opening disposed in the outer container, and a container produced according to this process, is described, wherein a pre-moulding, comprising two coaxial tubes, is first produced by co-extrusion with the help of a blow mould and with an outwardly-projecting base seam being formed. The process forms a pressure equalisation opening in the outer container without endangering the integrity of the container, wherein a lower wastage rate and higher productivity are achieved. To do this, the base seam is partially cut off and a force which acts in the direction of the seam is introduced into the pre-moulding, which has a temperature of 40 degrees C. to 70 degrees C., which force breaks open and plastically deforms the base seam so that a pressure equalisation opening is formed in the base area.

Abstract: The present invention relates to a method, a device, and a control program for the fluid-tight sealing of capsules containing medicaments, wherein the capsules consist of at least one capsule body and a capsule cap which are set one into the other telescopically and provided with a tight band in the abutment region on the exterior side of the capsule, wherein the capsule components are filled with gas which has a changed temperature and/or a changed pressure in relation to the environment, and wherein a reduction of the difference in pressure in the capsule occurs via gaps between capsule body and capsule cap after the capsule components have been placed one inside the other. The capsules produced via the method according to the invention are disposable capsules and preferably contain a single dose of an orally administered pharmaceutical formulation in the form of a powder or a liquid.

Abstract: Vaginal splints and methods for their use for treating various pelvic floor conditions are provided. One embodiment of the vaginal splint includes a base portion having a configuration defined by first and second sides, a first connecting portion at a proximal side of the base portion and extending between a first end of each of the first and second sides, and a second connecting portion at a distal side of the base portion and extending between a second end of each of the first and second sides. The splint further includes an adjustable portion coupled to the base portion and positioned substantially adjacent to and distal of the second connecting portion of the base portion. The adjustable portion is removable by a user to thereby change the size of the splint.

Abstract: Vaginal splint assemblies and methods for their use for treating various pelvic floor conditions are provided. One embodiment of a vaginal splint assembly includes a base portion having a connecting portion and first and second sides extending outwardly from first and seconds ends of the connecting portion to first and second free ends respectively. It further includes a plurality of apical sections each of a different size and each having a connecting portion and first and second sides extending outwardly from first and second ends of the connecting portion to first and second free ends respectively, and at least first and second coupling elements. The first coupling element is capable of securing the first free end of the base portion to the first free end of any one of the plurality of apical sections, and the second coupling element is capable of securing the second free end of the base portion to the second free end of the one apical section.

Abstract: Vaginal splints and methods for their use for treating various pelvic floor conditions are provided. One embodiment of the vaginal splint includes a base portion having a configuration defined by first and second sides, a first connecting portion at a proximal side of the base portion and extending between a first end of each of the first and second sides, and a second connecting portion at a distal side of the base portion and extending between a second end of each of the first and second sides. The splint further includes an adjustable portion coupled to the base portion and positioned substantially adjacent to and distal of the second connecting portion of the base portion. The adjustable portion is removable by a user to thereby change the size of the splint.

Abstract: Vaginal splints and methods for their use for treating various pelvic floor conditions are provided. One embodiment of the vaginal splint includes a base portion having a configuration defined by first and second sides, a first connecting portion at a proximal side of the base portion and extending between a first end of each of the first and second sides, and a second connecting portion at a distal side of the base portion and extending between a second end of each of the first and second sides. The splint further includes an adjustable portion coupled to the base portion and positioned substantially adjacent to and distal of the second connecting portion of the base portion. The adjustable portion is removable by a user to thereby change the size of the splint.

Abstract: A cannula implantation instrument for use with the delivery of guide wire based implants includes a handle having an open slot for receiving a guide wire and a cavity for receiving an implant pre-mounted on the guide wire, a cannula having an open slot for also receiving a guide wire and a sharpened tip for introducing the cannula and guide wire simultaneously into the vas deferens of a patient, and a guide wire on which an intra vas implant is pre-mounted. The instrument further includes a safety clip on the handle that secures the guide wire and/or implant to the handle until released by a physician. The cannula implantation instrument may be ergonomically formed to provide comfort and ease while being handled by the physician.

Abstract: A self-anchoring tissue lifting device for use with facial cosmetic reconstructive surgery includes an implant and a removable foil cover disposed on the implant. The implant includes an elongated mesh strip having a distal end on which is situated a tissue anchoring fleece material. Opposite lateral edges of the mesh material are preferably laser cut during the manufacturing process of the implant to provide a plurality of tissue engaging prickles along the longitudinal length of the implant. For treating the mid face and jowl, a stab incision is made within the hairline of the temple region of the patient and the device is applied from the temporal area to the peak of the ipsilateral cheek to capture the malar fat pad to correct midface abnormalities or the ptotic tissue causing the jowl.

Abstract: A device for degenerating a fibroid comprises a receptacle sized and shaped so as to receive a uterine artery therein and a vacuum source connected to the receptacle. The vacuum source is capable of creating a vacuum sufficient to draw a uterine artery into the receptacle, and to fold it in a manner that substantially obstructs blood flow therethrough. In a method of degenerating a fibroid, the aforesaid device is placed near a uterine artery, and a vacuum is applied to draw the uterine artery into the receptacle so that the uterine artery folds shut, thereby obstructing blood flow through the artery. The vacuum is applied for a time that is sufficient to degrade or kill the fibroid, after which the vacuum is released.

Abstract: A device for degenerating a fibroid comprises a gripper mechanism sized and shaped so as to grip a uterine artery and a rotating mechanism attached to the gripper mechanism. The rotating mechanism may be rotated so as to rotate said gripper mechanism, thereby twisting a gripped uterine artery so as to obstruct blood flow through the artery. In a method of degenerating a uterine fibroid, the aforesaid gripping device is used to catch hold of a uterine artery and is rotated in a direction so as to twist the uterine artery about itself, thereby obstructing blood flow to the uterine fibroid. The gripping device is held in place for a period of time needed to degenerate the fibroid.

Abstract: A process for the production of a container (1) comprising an outer container (2), an inner bag (3) disposed therein and a pressure equalisation opening (10) disposed in the outer container (2), and also a container (1) produced according to this process, is described, wherein firstly a pre-moulding, comprising two coaxial tubes, is first produced by co-extrusion with the help of a blow mould and with an outwardly-projecting base seam (5) being formed. The process is to form a pressure equalisation opening (10) in the outer container (2) of the container (1) without endangering the integrity of the container (1), wherein a lower wastage rate and higher productivity are to be achieved. This is attained by a process wherein the base seam (5) is partially cut off and a force which acts in the direction of the seam is introduced into the pre-moulding, which still has a temperature of 40° C. to 70° C.

Abstract: A medical device including an implant and inserter and a method for using the same. One embodiment includes an implant for implantation within a patient, and a first inserter for inserting the implant. The first inserter has a distal end region including a tissue penetrating distal tip, a proximal end region, a capture element located at the distal end region, and an implant holding element having a proximal end and a distal end. The distal end is removably received within the capture element, and the implant holding element further is movably coupled to the first inserter at a first location proximal of the capture element. The implant holding element extends from the first location at which it is movably coupled to the first inserter, and subsequently through the implant before being removably received within the capture element to thereby removably secure the implant to the insertion device.