Abstract: Apparatus, systems and methods are disclosed for treating a biological fluid with light. A container of biological fluid is introduced into a fluid treatment chamber where it is contacted with light provided by one or more light sources in proximity to the fluid treatment chamber. A drawer for holding containers of biological fluid introduces the containers into the chamber. Containers for holding the biological fluid are marked by the apparatus to indicate the status of the treatment.

Abstract: A solution applicator includes a container, a head and a cap. The head includes a top portion for use in applying the solution, a spike member which is used to pierce or open a membrane and at least one protrusion extending from the head. The cap includes a top portion that receives the spike member, a bottom portion that connects to the container and a middle portion that defines a circumferential channel and an axial channel. The protrusion is received within the circumferential channel and the axial channel such that the head can be moved relative to the cap in first a rotational motion and then an axial motion to open the solution container.

Abstract: Apparatus, systems and methods are disclosed for treating a biological fluid with light. A container of biological fluid is introduced into a fluid treatment chamber where it is contacted with light provided by one or more light sources in proximity to the fluid treatment chamber. A drawer for holding containers of biological fluid introduces the containers into the chamber. Containers for holding the biological fluid are marked by the apparatus to indicate the status of the treatment.

Abstract: Apparatus, systems and methods are disclosed for treating a biological fluid with light. A container of biological fluid is introduced into a fluid treatment chamber where it is contacted with light provided by one or more light sources in proximity to the fluid treatment chamber. A drawer for holding containers of biological fluid introduces the containers into the chamber. Containers for holding the biological fluid are marked by the apparatus to indicate the status of the treatment.

Abstract: A solution applicator includes a container, a head and a cap. The head includes a top portion for use in applying the solution, a spike member which is used to pierce or open a membrane and at least one protrusion extending from the head. The cap includes a top portion that receives the spike member, a bottom portion that connects to the container and a middle portion that defines a circumferential channel and an axial channel. The protrusion is received within the circumferential channel and the axial channel such that the head can be moved relative to the cap in first a rotational motion and then an axial motion to open the solution container.

Abstract: The invention herein provides an improved manufacturing process for sterile containers pre-filled with topical antimicrobial solutions that reduces or avoids undesirable by-products as a result of the ethylene oxide gas sterilization technique. The process of the invention produces containers pre-filled with antimicrobial solution that are sterilized in accordance with the ethylene oxide technique, while at the same time have a toxic residue content within acceptable limits. The invention is particularly useful in the manufacture of plastic containers pre-filled with iodine-based antimicrobial solutions.

Abstract: The invention described herein is a sterile, disposable ophthalmic surgery preparation system and technique that can be introduced directly into the sterile field of surgical preparation without significantly compromising sterile conditions. Both the antimicrobial solution and the container holding the solution can be presented into the sterile field in sterile condition. The antimicrobial solution and container are dimensioned and proportioned for single patient or single procedure usage. The invention includes a sterile, disposable ophthalmic surgery preparation system comprising: a sealed, rupturable flexible container structured as a dropper; the container being filled with a liquid antimicrobial composition formulated for ophthalmic application; wherein the container and composition are proportioned for single application use. The invention further provides a surgical kit and method of preparing a patient for ophthalmic surgery.

Abstract: A dispensing and application apparatus designed to contain pre-measured amounts of a flowable substance. The apparatus comprises a compartment 130 for storing the substance that is partially enclosed by a frangible seal 210, an applicator 100, and an expandable chamber 170 designed to accept and dissipate the hydraulic force created when pressure is applied to the compartment 130, rupturing the frangible seal 210, and expelling the substance into the chamber 170. The applicator 100 is attached to the chamber 170 with an applicator bond area 180. The expandability of the chamber 170 is conferred by expandability of the applicator 100, and is varied in different embodiments by altering the ratio between the area of the applicator bond area 180 and the area of the applicator 100. The frangible seal 210, in one of many embodiments, may be a chevron shape stress riser 250 with a point of inflection 240 oriented towards the compartment 130. A removable cap may cover the applicator.

Abstract: A dispensing and application apparatus designed to contain pre-measured amounts of a flowable substance. The apparatus comprises a compartment 130 for storing the substance that is partially enclosed by a frangible seal 210, an applicator 100, and an expandable chamber 170 designed to accept and dissipate the hydraulic force created when pressure is applied to the compartment 130, rupturing the frangible seal 210, and expelling the substance into the chamber 170. The applicator 100 is attached to the chamber 170 with an applicator bond area 180. The expandability of the chamber 170 is conferred by expandability of the applicator 100, and is varied in different embodiments by altering the ratio between the area of the applicator bond area 180 and the area of the applicator 100. The frangible seal 210, in one of many embodiments, may be a chevron shape stress riser 250 with a point of inflection 260 oriented towards the compartment 130. A removable cap may cover the applicator.

Abstract: A dispensing and application apparatus designed to contain pre-measured amounts of a flowable substance. The apparatus comprises a compartment 130 for storing the substance that is partially enclosed by a frangible seal 210, an applicator 100, and an expandable chamber 170 designed to accept and dissipate the hydraulic force created when pressure is applied to the compartment 130, rupturing the frangible seal 210, and expelling the substance into the chamber 170. The applicator 100 is attached to the chamber 170 with an applicator bond area 180. The expandability of the chamber 170 is conferred by expandability of the applicator 100, and is varied in different embodiments by altering the ratio between the area of the applicator bond area 180 and the area of the applicator 100. The frangible seal 210, in one of many embodiments, may be a chevron shape stress riser 250 with a point of inflection 240 oriented towards the compartment 130. A removable cap may cover the applicator.

Abstract: Apparatus, systems and methods are disclosed for treating a biological fluid with light. A disposable fluid processing set including integrally connected containers and tubing and a holder or organizer for receiving at least some of the containers and tubing are disclosed.

Abstract: Apparatus, systems and methods are disclosed for treating a biological fluid with light. A container of biological fluid is introduced into a fluid treatment chamber where it is contacted with light provided by one or more light sources in proximity to the fluid treatment chamber. A drawer for holding containers of biological fluid introduces the containers into the chamber. Containers for holding the biological fluid are marked by the apparatus to indicate the status of the treatment.

Abstract: Containers and methods for making containers are disclosed. The containers include a chamber and a pouch fixed within the chamber. During manufacture, the open edges of the pouch are sealed between the walls of the container by a seal defining, in part, the peripheral edge of the chamber.

Abstract: Disclosed is a system for administering epidural anesthesia utilizing an epidural catheter permanently secured at its proximal end to an adapter for putting the catheter in fluid communication with a source of liquid anesthesia. The system employs a splittable needle for inserting the catheter into the peridural space.

Abstract: Disclosed is a splittable needle device adapted for use in administering epidural anesthesia. The needle has guide means to facilitate insertion of the needle into the peridural space, contained on a splittable hub assembly.

Abstract: A liquid drainage system is disclosed comprising a combination urine meter element and drainage receptacle, the urine meter element having front and rear walls defining a chamber adapted to receive and measure urine output.

Abstract: An ostomy appliance including a collection pouch, an adhesive faceplate for adherence to a patient, and a coupling ring assembly detachably connecting the pouch and faceplate together. The coupling ring assembly comprises a pair of flexible plastic latching rings capable of being connected together by axially-applied forces and a soft, deformable, sealing ring interposed between, and axially compressed by, opposing wall portions of the latching rings.

Abstract: An external male catheter having an elastic sheath section and a receiving section connected together when the device is used as an external catheter but constructed to permit detachment of the receiving section, while retaining the sheath section in adhesive attachment to the wearer, to permit direct access to the urethral meatus for intermittent internal catherization.

Abstract: A coupling for an ostomy appliance that detachably joins an ostomy bag to a faceplate capable of being adhesively secured to a patient's skin about a stoma opening. Each coupling ring is formed of flexible and resilient thermoplastic material, with one of the rings having an axially-extending frusto-conical neck portion and the other ring having a frusto-conical collar portion detachably receiving and sealingly engaging the neck portion. Primary latching is achieved in an annular zone spaced a substantial distance radially outwardly from the area of sealing engagement between the neck and collar portions, such latching action being provided by a shoulder extending about the outer periphery of one of the rings and a latching rib, defining a shoulder-receiving recess, extending about the outer periphery of the other ring.