Appliance to be implanted, method of collapsing the appliance to be implanted and method of using the appliance to be implanted
First Claim
1. The appliance to be implanted, comprising a front end wire ring, a rear end wire ring arranged facing to said front end wire ring, a tubular cover which connects said front end wire ring and said rear end wire ring, and a plurality of intermediate wire rings spaced apart from each other between the front end wire ring and the rear end wire ring, in which each of the wire rings is given flexibly foldable elasticity, characterized in that the circumference of said front end wire ring and said intermediate wire rings are equally divided into four or an even number over four segments with dividing points between said segments, that hooking means are formed for a front pull string to be passed through every other dividing point between said segments in said front end wire ring and that the circumference of the intermediate wire rings are fixed to the tubular cover by suturing or with adhesive only at positions which correspond to midpoints between each adjacent two of the dividing points on said intermediate wire rings, said midpoints on said front end wire ring and said intermediate wire rings being in alignment.
0 Assignments
0 Petitions
Accused Products
Abstract
The artificial blood vessel A comprises a front end wire ring 101, a rear end wire ring 102 arranged facing to the front end wire ring 101, a tubular cover 7 which connects the end wire rings 101, 102, and a plurality of intermediate wire rings 12 arranged spaced apart from each other between the front end wire ring 101 and the rear end wire ring 102. Each of the front end wire ring 101, the rear end wire ring 102 and the intermediate wire rings 12 are given flexibly foldable elasticity. The circumference of the front end wire ring 101 is equally divided into four by dividing points 411, 421, 431, 441. Hooking devices 13 are formed for a front pull string to be passed through at the dividing points 411, 431. The circumference of the intermediate wire ring 12 is fixed to the tubular cover 7 by suturing or with adhesive at the positions 513, 523, 533, 543 which correspond to the midpoint 511 between the dividing points 411, 421, the midpoint 521 between the dividing points 421, 431, the midpoint 531 between the dividing points 431, 441, and the midpoint 541 between the dividing points 441, 411.
-
Citations
5 Claims
- 1. The appliance to be implanted, comprising a front end wire ring, a rear end wire ring arranged facing to said front end wire ring, a tubular cover which connects said front end wire ring and said rear end wire ring, and a plurality of intermediate wire rings spaced apart from each other between the front end wire ring and the rear end wire ring, in which each of the wire rings is given flexibly foldable elasticity, characterized in that the circumference of said front end wire ring and said intermediate wire rings are equally divided into four or an even number over four segments with dividing points between said segments, that hooking means are formed for a front pull string to be passed through every other dividing point between said segments in said front end wire ring and that the circumference of the intermediate wire rings are fixed to the tubular cover by suturing or with adhesive only at positions which correspond to midpoints between each adjacent two of the dividing points on said intermediate wire rings, said midpoints on said front end wire ring and said intermediate wire rings being in alignment.
Specification