Abstract: Provided is an aqueous composition for ophthalmic or nasal administration comprising levocetirizine or its salt. In one embodiment, the composition comprises levocetirizine or its salt at a levocetirizine concentration of 0.05-0.5% (w/v). The composition may further comprise a surface active agent and/or an organic acid salt.

Abstract: The present invention relates to an inflator mounted on protective equipment, comprising: a main body (100) having a cylindrical structure that is open at the top and bottom thereof, wherein the main body (100) has a key-ball insertion hole (110) and a gas supply hole (120) that are formed on portions of a lateral side thereof, and a bomb (600) for storing compressed air is coupled to the lower side of the main body (100); an eccentric lever (200) that is rotatably coupled to the upper opening of the main body (100) through a rotation shaft (230) and includes a lever (210) that adjusts a downward pressure by rotating an eccentric drum part (220) having the shape of a circular plate; a perforation part (300) that provides a restoring force downward according to the pressure state of the eccentric lever (200) and perforates the bomb (600) to allow the gas in the bomb (600) to be supplied to a user's protective equipment through the gas supply hole (120); and a key-ball (400) that confines the movement of the pe

Abstract: At the time of blood sampling, blood collection tube information of a blood collection tube concerned is read by blood-collection-tube information reading means, and blood collection subject information 20 on an identification belt as an information recording medium carried by the blood collection subject is read by information-recording-medium reading means. The respectively-read blood collection tube information of the blood collection tube concerned and blood collection subject information of the blood collection subject concerned are correlated with each other and stored in a storage unit by information management means.

Abstract: Provided is a device for strengthening a pelvic floor muscle. The device for strengthening a pelvic floor muscle includes a device body provided with a seating means on which a user can sit; and two or more electrode pads for applying a low frequency pulse, the electrode pads being disposed around a portion of the device body corresponding to the user's anus. In addition, a method for controlling the device for strengthening a pelvic floor muscle includes separately applying the generated low frequency pulse in a ramp up (Ru) time, a hold (Ht) time and a ramp down (Rd) time.

Abstract: Provided is a device for strengthening a pelvic floor muscle. The device for strengthening a pelvic floor muscle includes a device body provided with a seating means on which a user can sit; and two or more electrode pads for applying a low frequency pulse, the electrode pads being disposed around a portion of the device body corresponding to the user's anus. In addition, a method for controlling the device for strengthening a pelvic floor muscle includes separately applying the generated low frequency pulse in a ramp up (Ru) time, a hold (Ht) time and a ramp down (Rd) time.

Abstract: The present invention relates to a composition comprising ethanol, polyol, salicylic acid, triclosan, allantoin, licorice acid or its di-alkali metallic salt, dl-camphor, houttynia cordata extract, green tea extract, and aloe extract as main ingredients and water and perfume essence as auxiliary ingredients. The present composition has excellent elimination effect of offensive odors caused by sweat.

Abstract: The present invention relates to a composition comprising ethanol, polyol, salicylic acid, triclosan, allantoin, licorice acid or its di-alkali metallic salt, dl-camphor, houttynia cordata extract, green tea extract, and aloe extract as main ingredients and water and perfume essence as auxiliary ingredients. The present composition has excellent elimination effect of offensive odors caused by sweat.

Abstract: In a medical guide wire 1, a rear half of a leading bulge portion (ellipsoidal helical spring) 5 forms a truncated cone shaped front catheter engagement portion 8. An inner wall of a balloon catheter 2 forms a flared end portion 2A which absorbably fits into the front catheter engagement portion 8 due to the physical adhesion so to provisionally connect the balloon catheter 2 to the front catheter engagement portion 8. The medical guide wire 1 and the balloon catheter 2 are inserted into the blood vessel with one single step procedure when the medical guide wire 1 is introduced into the blood vessel to place the balloon portion 10 at the stricture blood vessel area (P).

Abstract: The present invention is directed by a capacitor comprising of dielectrics formed of a plastic film in which ceramic particles are dispersed. The plastic film is manufactured by the processes comprising the steps of coating the ceramic particles with wax, dispersing the wax-coated ceramic particles in a molten plastic, and extruding the molten plastic in which ceramic particles are dispersed into a think film.

Abstract: The present invention is directed by a capacitor comprising of dielectrics formed of a plastic film in which ceramic particles are dispersed. The plastic film is manufactured by the processes comprising the steps of coating the ceramic particles with wax, dispersing the wax-coated ceramic particles in a molten plastic, and extruding the molten plastic in which ceramic particles are dispersed into a think film.

Abstract: With an introducing catheter (A) accommodated by a diagnostic-therapeutic catheter (B), the necessity of a sheath is eliminated to render the diagnostic-therapeutic catheter (B) as large as the sheath. This enables a manipulator to fully treat a patient with the use of diagnostic-therapeutic catheter (E). With the elimination of the sheath, the diagnostic-therapeutic catheter (B) is directly inserted into tubular human organs (e.g., radial artery and brachial artery). Coaxially provided are inner and outer tubes 12, 13 with the diagnostic-therapeutic catheter (B) to have an annular space 14, at least a part of which forms a drug-releasable open end 15 exposed to a shaft portion 11. The outer tube 13 has a plurality of drug-releasable side holes 9 to release an anti-spasmodic drug toward a blood vessel through the drug-releasable open end 15.

Abstract: A cable sleeve system for bone fixation, comprising a cable, and a sleeve including a head for securing the cable and a piercing portion, wherein the piercing portion projects from a bottom face of the head substantially perpendicularly therefrom, and the head is provided with a bore extending in parallel with the bottom face for securing the cable therein, the head being adapted to be crimped to secure the cable therein. Because the sleeve can be made highly compact, it is possible to avoid undesirable side effects such as hemorrhage and inflammation due to irritations to the human body tissues which occurred frequently in the case of the cable securing method using the conventional cable grip.

Abstract: In a medical guide wire 1, a rear half of a leading bulge portion (ellipsoidal helical spring) 5 forms a truncated cone shaped front catheter engagement portion 8. An inner wall of a balloon catheter 2 forms a spiral groove 9. The spiral groove 9 fits into the front catheter engagement portion 8 to provisionally connect the balloon catheter 2 to the front catheter engagement portion 8. The medical guide wire 1 and the balloon catheter 2 are inserted into the blood vessel with one single step procedure when the medical guide wire 1 is introduced into the blood vessel to place the balloon portion 10 at the stricture blood vessel area (P) to cure the stricture blood vessel area (P).