Abstract: A lacrimal duct tube includes: a pair of tubular members that each have at one end an opening communicating with a lumen; and a connection member that connects the other ends of the tubular members. A base end part including the other end of at least one of the tubular members is tapered down toward the connection member and the base end part has an inlet/outlet port communicating with the lumen of the tubular member. A portion of the base end part constituting peripheral edge of the inlet/outlet port and the connection member are connected together.

Abstract: A medical tube in which an intermediate layer composed of a composition containing (a), (b), and (c1) listed below and a lubricant layer composed of a composition containing (a), (b), and (c2) listed below are sequentially laminated on a surface of an insertion member to be inserted into a living body: (a) 1 to 35 weight % of at least one of aromatic diisocyanate, aliphatic diisocyanate, and alicyclic diisocyanate; (b) 1 to 35 weight % of trifunctional or higher functionality polyol; (c1) 30 to 98 weight % of polyalkylene glycol and/or monomethoxypolyalkylene glycol; and (c2) 30 to 98 weight % of polyalkylene glycol (including polyalkylene glycol larger in weight-average molecular weight than polyalkylene glycol in (c1)) and/or monomethoxypolyalkylene glycol (including monomethoxypolyalkylene glycol larger in weight-average molecular weight than monomethoxypolyalkylene glycol in (c1)), (where each of the glycols in (c1) and (c2) is diol).

Abstract: A lacrimal duct tube includes: a pair of tubular members that each have at one end an opening communicating with a lumen and have in a wall a hole for guiding a lacrimal duct tube operative instrument to the lumen; and a connection member that connects the other ends of the tubular members. Surfaces of the tubular members include a hydrophilic-coated portion and a non-coated portion without the hydrophilic coating. It is preferred that the lumen in the vicinity of the opening includes an engagement portion for engagement with a tip of the lacrimal duct tube operative instrument, and the non-coated portion is formed without overlapping with the surface of the tubular member at the position of the engagement portion. The lacrimal duct tube can be used favorably for various lacrimal duct obstruction treatments. In the case of using a sheath such as in sheath guided endoscopic probing, the lacrimal duct tube can be easily inserted into the sheath and be firmly fixed to the sheath.

Abstract: A lacrimal duct tube including: a pair of tubular members each of which has an terminal end opening at one end; and a central member that connects other ends of the tubular members, at least one of the tubular members includes: a cylindrical part extended from the terminal end opening to the central member side and has an opening for bar-like operative instrument at an end portion at the central member side; and an arc-shaped part that is extended from the end portion of the cylindrical part at the central member side further to the central member side and has an almost arc-shaped wall portion on a cross section orthogonal to a longitudinal side of the tubular member, and the almost arc-shaped wall portion is formed at the arc-shaped part continuously over a length of ? or more and 9/10 or less of an entire length of the tubular member.

Abstract: The present invention provides a lacrimal duct tube that can be preferably used for the treatment of lacrimal duct obstruction, in particular, sheath guided endoscopic probing having been frequently performed in recent years, the lacrimal duct tube being excellent in passage through a lesion in the lacrimal duct, operability in the lacrimal duct, and manipulation of the endoscope inserted into the lumen of the tube, and providing a sufficient viewing field of the endoscope. The present invention relates to a lacrimal duct tube, including: a pair of tubular members that each has an opening at one end and a hole in a side wall communicating with a lumen; and a connection member that connects other ends of the tubular members, wherein the tubular members each include a plurality of resin portions different in Shore hardness, at least one of the resin portions is positioned between the opening and the hole and forms a lumen wall of the tubular member, and the lumen wall has a Shore hardness of 57D or more.

Abstract: A lacrimal duct tube includes: a pair of tubular members that each have at one end an opening communicating with a lumen and have in a wall a hole for guiding a lacrimal duct tube operative instrument to the lumen; and a connection member that connects the other ends of the tubular members. Surfaces of the tubular members include a hydrophilic-coated portion and a non-coated portion without the hydrophilic coating. It is preferred that the lumen in the vicinity of the opening includes an engagement portion for engagement with a tip of the lacrimal duct tube operative instrument, and the non-coated portion is formed without overlapping with the surface of the tubular member at the position of the engagement portion. The lacrimal duct tube can be used favorably for various lacrimal duct obstruction treatments. In the case of using a sheath such as in sheath guided endoscopic probing, the lacrimal duct tube can be easily inserted into the sheath and be firmly fixed to the sheath.

Abstract: A lacrimal duct tube includes: a pair of tubular members that each have at one end an opening communicating with a lumen; and a connection member that connects the other ends of the tubular members. A base end part including the other end of at least one of the tubular members is tapered down toward the connection member and the base end part has an inlet/outlet port communicating with the lumen of the tubular member. A portion of the base end part constituting peripheral edge of the inlet/outlet port and the connection member are connected together.

Abstract: A lacrimal duct tube including: a pair of tubular members each of which has an terminal end opening at one end; and a central member that connects other ends of the tubular members, at least one of the tubular members includes: a cylindrical part extended from the terminal end opening to the central member side and has an opening for bar-like operative instrument at an end portion at the central member side; and an arc-shaped part that is extended from the end portion of the cylindrical part at the central member side further to the central member side and has an almost arc-shaped wall portion on a cross section orthogonal to a longitudinal side of the tubular member, and the almost arc-shaped wall portion is formed at the arc-shaped part continuously over a length of ? or more and 9/10 or less of an entire length of the tubular member.

Abstract: The present invention provides a lacrimal duct tube that can be preferably used for the treatment of lacrimal duct obstruction, in particular, sheath guided endoscopic probing having been frequently performed in recent years, the lacrimal duct tube being excellent in passage through a lesion in the lacrimal duct, operability in the lacrimal duct, and manipulation of the endoscope inserted into the lumen of the tube, and providing a sufficient viewing field of the endoscope. The present invention relates to a lacrimal duct tube, including: a pair of tubular members that each has an opening at one end and a hole in a side wall communicating with a lumen; and a connection member that connects other ends of the tubular members, wherein the tubular members each include a plurality of resin portions different in Shore hardness, at least one of the resin portions is positioned between the opening and the hole and forms a lumen wall of the tubular member, and the lumen wall has a Shore hardness of 57D or more.

Abstract: A medical tube in which an intermediate layer composed of a composition containing (a), (b), and (c1) listed below and a lubricant layer composed of a composition containing (a), (b), and (c2) listed below are sequentially laminated on a surface of an insertion member to be inserted into a living body: (a) 1 to 35 weight % of at least one of aromatic diisocyanate, aliphatic diisocyanate, and alicyclic diisocyanate; (b) 1 to 35 weight % of trifunctional or higher functionality polyol; (c1) 30 to 98 weight % of polyalkylene glycol and/or monomethoxypolyalkylene glycol; and (c2) 30 to 98 weight % of polyalkylene glycol (including polyalkylene glycol larger in weight-average molecular weight than polyalkylene glycol in (c1)) and/or monomethoxypolyalkylene glycol (including monomethoxypolyalkylene glycol larger in weight-average molecular weight than monomethoxypolyalkylene glycol in (c1)), (where each of the glycols in (c1) and (c2) is diol).

Abstract: A lacrimal duct tube (31) includes an integrated tube that is placed in a lacrimal duct and capable of insertion of an insertion aid (36) in a detachable manner. The tube (31) has a terminal end opening (33) at a terminal end. In the vicinity of the terminal end opening (33), a stopper part (32a, 32b, 32c, and 32d) for stopping the insertion aid (36) is inserted in the tube (31). The stopper part (32a, 32b, 32c, and 32d) is opened at both ends in an axial direction of the tube and has a cylindrical structure including an inner wall surface (37a, 37b, 37c, and 37d) to guide and stop the insertion aid (36).

Abstract: A tube device for insertion into a lacrimal passage, optimized according to the structure of a lacrimal passage and capable of being operated without impairing the functional effect of a lacrimal passage endoscope. A tube device for insertion into a lacrimal passage comprises a pair of tubes to be placed in the lacrimal passage. Openings are formed at both ends of the pair of tubes. A reinforcement body is disposed and held in the vicinity of each opening at a position located at a predetermined distance from the opening.

Abstract: Disclosed is a resin composition for balloons, which is excellent in gas permeation resistance and hydrolysis resistance (acid resistance), while having an excellent balance among flexibility, mechanical strength and elastic recoverability. Also disclosed is a balloon made of such a resin composition for balloons. Specifically disclosed is a resin composition for balloons, which is characterized by containing an isobutylene block copolymer (A) having a polymer block (a) mainly composed of isobutylene and a polymer block (b) mainly composed of an aromatic vinyl monomer. This resin composition for balloons is also characterized in that the polymer block (b) is 10-40% by weight of the weight of the isobutylene block copolymer (A).

Abstract: A guide wire which includes: (a) a core wire formed with a mounting portion at the distal end portion; and (b) a plurality of coil wires being fitted onto the mounting portion substantially in tandem, and having different mechanical properties, the adjacent coil wires being connected with each other at the corresponding ends thereof. One of the corresponding ends of the adjacent coil wires is formed into a tapered portion gradually reducing in outer diameter toward said end. The other one of the corresponding ends is formed into a receiving end portion into which the tapered portion is inserted.

Abstract: A guide wire which includes: (a) a core wire formed with a mounting portion at the distal end portion; and (b) a plurality of coil wires being fitted onto the mounting portion substantially in tandem, and having different mechanical properties, the adjacent coil wires being connected with each other at the corresponding ends thereof. One of the corresponding ends of the adjacent coil wires is formed into a tapered portion gradually reducing in outer diameter toward said end. The other one of the corresponding ends is formed into a receiving end portion into which the tapered portion is inserted.

Abstract: A protector for housing a drug administration needle comprised of a winged hub and a cannula bent substantially perpendicular to a longitudinal axis of the hub at a longitudinal central portion of the hub. The protector comprises a tubular cannula-protecting portion having a cannula entrance at one end and a bottom at the opposite end; and a hub-mounting portion for attachment of the winged hub, the hub-mounting portion being coaxially formed on the cannula entrance of the cannula-protecting portion.

Abstract: A protector for housing a drug administration needle comprised of a winged hub and a cannula bent substantially perpendicular to a longitudinal axis of the hub at a longitudinal central portion of the hub. The protector comprises a tubular cannula-protecting portion having a cannula entrance at one end and a bottom at the opposite end; and a hub-mounting portion for attachment of the winged hub, the hub-mounting portion being coaxially formed on the cannula entrance of the cannula-protecting portion.

Abstract: A catheter body includes a main lumen and an auxiliary lumen. The main lumen has an outlet opening located at a distal end of the body and an inlet opening at a proximal end. The auxiliary lumen has an outlet opening located behind and spaced from the distal end a distance of 5-10 cm and an inlet lateral opening located toward the proximal end. An adapter for providing inlet ports communicating with the inlet openings of the main lumen and auxiliary lumen is provided on the catheter body. The adapter includes three members detachably connected to one another. The forward and middle members have threaded portions which engage one another and the middle and rearward members also have threaded portions which engage with one another. Annular seals are provided between the forward and middle members and the middle and rearward members. The adapter can be readily attached to the catheter body and an external device for dosing a liquid medicine can be attached to the adapter.

Abstract: An apparatus for dosing a liquid medicine has a balloon (1), a housing (3) and a delivery assembly `b`. The balloon receives and discharges a liquid medicine under pressure. The housing enclosing the balloon has an opening communicating with the assembly `b` in which a flow regulator (10) is installed. The balloon (1) is composed of flat and expansible sheets secured to both side rims of a short cylindrical frame (2). The flat sheets constituting the balloon are of an even thickness over their whole area, even after being inflated with the medicine, so that the pressure as well as the flow rate of the medicine effluent from the balloon will scarcely vary at the mouth over the course of time. Thus, the liquid medicine is dosed to a patient at a constant flow rate through the regulator.

Abstract: This invention concerns inspection of surface conditions to detect locations, sizes and nature of flaws, defects or stains not only on a flat surface but also on an undulating or stepped surface, and includes the steps of: scanning an inspecting surface of a specimen with a spot-like laser beam projected obliquely from a light source; detecting the height of the inspecting surface from a reflected image of the scanning light picked up by a TV camera located above the inspecting surface, to maintain the inspecting surface at a constant height; converging reflected and diffracted light from the inspecting surface toward a photo-detector having measuring points at the point of convergence and at a number of positions along a concentric circle around the point of convergence; measuring the energy of the reflected and diffracted light by photoelectric transducers connected to the respective measuring points; and displaying locations, sizes and nature of surface flaws, defects and stains of the specimen on a monito