STENT AND LIVING ORGAN DILATOR
First Claim
1. A stent configured to closely contact tissue in vivo by being deformed when set indwelling in vivo, the stent comprising:
- a plurality of linear components configured to deform and exhibit a force for maintaining dilation when the stent is set indwelling in vivo, the linear components comprising a plurality of non-biodegradable metallic linear components and a plurality of biodegradable material-made linear components, the biodegradable material-made linear components being bonded to the non-biodegradable metallic linear components;
both the non-biodegradable metallic linear components and the biodegradable material-made linear components contributing to the stent exhibiting the force for maintaining the dilation when the stent is left indwelling in vivo; and
after a predetermined period of time following the stent being left indwelling in vivo, biodegradation of the biodegradable material-made linear components proceeds so that the force for maintaining the dilation is lowered.
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Accused Products
Abstract
A stent, composed of linear components, comes into close contact with a tissue in vivo upon being deformed when set indwelling in vivo. The stent has linear components which are deformed to exhibit a force for maintaining dilation when the stent is set indwelling in vivo. The linear components deformed when the stent is set indwelling in vivo are composed of non-biodegradable metallic linear components and a plurality of biodegradable material-made linear components which are bonded to the non-biodegradable metallic linear components. Furthermore, when set indwelling in vivo, the stent exhibits the force for maintaining the dilation owing to both the non-biodegradable metallic linear components and the biodegradable material-made linear components. After a predetermined period of time, biodegradation of the biodegradable material-made linear components proceeds, which results in a lowering of the force for maintaining the dilation
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Citations
35 Claims
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1. A stent configured to closely contact tissue in vivo by being deformed when set indwelling in vivo, the stent comprising:
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a plurality of linear components configured to deform and exhibit a force for maintaining dilation when the stent is set indwelling in vivo, the linear components comprising a plurality of non-biodegradable metallic linear components and a plurality of biodegradable material-made linear components, the biodegradable material-made linear components being bonded to the non-biodegradable metallic linear components; both the non-biodegradable metallic linear components and the biodegradable material-made linear components contributing to the stent exhibiting the force for maintaining the dilation when the stent is left indwelling in vivo; and after a predetermined period of time following the stent being left indwelling in vivo, biodegradation of the biodegradable material-made linear components proceeds so that the force for maintaining the dilation is lowered. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35)
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Specification