Abstract:
A protective apparatus for a chemotherapy injection needle, includes a coring needle, a plastic film integrated with a hand-held film, and an injection vessel, wherein the coring needle is a through, hollow and metal needle having a needle head bent downwards to form an angle with a needle body which connects to the injection vessel at a rear end. The plastic film has two trapezoidal and protruding wings extending to two sides, and when the two protruding wings are folded to clamp the needle head, the protruding wings' extending length is sufficient to wrap a tip part of the needle head, and positions where the protruding wings wrap the tip part are corresponding to concaved grooves of the needle head, so that the two protruding wings attach closely with each other. Also, the two protruding wings engage with each other by a locking device to secure the protruding wings.
Abstract:
A totally implantable venous device includes a port comprising an arcuate housing having a recess on an inner surface and an opening being in communication with the recess, the opening having a flat mouth, an internal chamber, and a base formed of hard plastic and being capable of preventing a needle from inserting through; a catheter comprising a fastening member at one end; a sleeve complementarily mounted on a front portion of the fastening member; and a sleeving member complementarily mounted on the remaining portion of the fastening member. The recess and the opening form a through hole having an enlarged intermediate portion. The fastening member has a truncated trapezoidal shape. The sleeve, the sleeving member, and the fastening member form a watertight structure at the recess and the opening. The catheter and the fastening member are formed of the same material.
Abstract:
A device for positioning tracheostomy tube includes a tracheostomy tube and a tracheostomy tube protecting membrane. The tracheostomy tube protecting membrane includes a tearing line portion formed at two sides of the tracheostomy tube protecting membrane. The tracheostomy tube protecting membrane is used for mounting in a trachea of a patient to form a positioning path for the tracheostomy tube. The tearing line portion is used for being torn open and removed. The present invention utilizes the tracheostomy tube protecting membrane to be mounted in a trachea of a patient first. The tracheostomy tube protecting membrane can effectively protect the trachea of the patient.
Abstract:
An implantable venous device is provided with a catheter including a passage; a locking nut including a channel for receipt of the catheter, and an annular convex end; an injection seat including a base, a peripheral wall, and a mounting member projecting out of the wall; a connecting tube projecting out of the mounting member and including a bulged central portion and an annular curved outward end wherein the locking nut is secured onto the bulged central portion; a base member including a groove; a housing including a top opening, a clamping portion on a periphery of the top opening, and a passageway through a bottom edge for receipt of the base member wherein the injection seat is fastened in the housing, and the locking nut is in the groove; and an implant member in the top opening and including a peripheral flange urged downward by the clamping portion.
Abstract:
A positioning device for a stent includes a positioning member including a handle and an extension secured to the handle wherein the handle and the extension are coaxially connected, and an open end of the extension is provided with a hollow first magnetic member; and a stent inserted into a blood vessel and including a first stent member inserted into an artificial blood vessel, the first stent member being separated into two second stent members inserted into the artificial blood vessel wherein a diameter of the first stent member is greater than that of each second stent member, and a diameter of each second stent member is greater than that of the extension, the stent further comprising at least one second magnetic member on the first stent member proximate an open end thereof, the second magnetic member being configured to attach to the first magnetic member.
Abstract:
An abdominal aortic stent includes a first sub-stent and a second sub-stent each having a front end. The circumference of the front end of each sub-stent is half of the circumference of the abdominal aorta. When the circumference is gradually reduced to a rear end of each sub-stent, it has entered one side of the bilateral femoral arteries. The rear ends of the sub-stents with full circumference of the cross-sectional area of the femoral artery are included therein. The first and second sub-stents are coated with external removable membrane to compress the sub-stents to generate smaller circumferences. When the removable membrane has been removed, the sub-stents are fully extended to reconstruct the vascular flow path.
Abstract:
An abdominal aortic stent includes a first sub-stent and a second sub-stent, each having a front end and the circumference of the front end of each sub-stent is half of the circumference of the abdominal aorta, and when the circumference is gradually reduced to a rear end of each sub-stent, it has entered one side of the bilateral femoral arteries, wherein the rear ends of the sub-stents with full circumference of the cross-sectional area of the femoral artery are included therein; the first and second sub-stents are coated with external removable membrane to compress the sub-stents to generate smaller circumferences, and when the membrane has been removed, the sub-stents are fully extended to reconstruct the vascular flow path.
Abstract:
An auxiliary chamber for inhaled-drugs includes a hollow tube body and a hollow side tube; and a unidirectional air valve which only allows air from an inlet flowing to an outlet end is located at the inlet end of the hollow tube body, wherein the outlet end of the hollow tube body is connected to an endotracheal tube. The hollow side tube connects with a lateral hole of the hollow tube body at one end, and a special universal adapter at the other end. The special universal adapter has a small through hole which is used to accommodate an inhaler therein to release inhaled drugs in the inhaler into the hollow tube body, and the inhaled drugs moves from the inlet end with air flow to the outlet end after entering the hollow tube body to help patients with respiratory failure take medicine.
Abstract:
An abdominal aortic stent includes a first sub-stent and a second sub-stent, each having a front end and the circumference of the front end of each sub-stent is half of the circumference of the abdominal aorta, and when the circumference is gradually reduced to a rear end of each sub-stent, it has entered one side of the bilateral femoral arteries, wherein the rear ends of the sub-stents with full circumference of the cross-sectional area of the femoral artery are included therein; the first and second sub-stents are coated with external removable membrane to compress the sub-stents to generate smaller circumferences, and when the membrane has been removed, the sub-stents are fully extended to reconstruct the vascular flow path.
Abstract:
A natural orifice translumenal endoscopic surgery (NOTES) device includes a puncture needle, dilator sheaths and working sheaths. The puncture needle includes a puncture end and a protruding safety stud situated substantially at a middle section of the puncture needle. Each dilator sheath has an insert end and a position limit end, and each dilator is sheathed sequentially onto the puncture needle, and the position limit end is stopped by the safety stud of the puncture needle, such that the insert end will not exceed the puncture end and will form a safety interval from the puncture end. The working sheath is provided for inserting and retracting the dilator sheaths and the puncture needle to form a space required for a surgical operation after the dilator sheaths have expanded a natural orifice, so as to provide a safe and convenient use of NOTES.