Abstract: A surgical drape has a fenestration configured to aid in identifying an anatomical point of interest and positioning the fenestration at the surgical site. In one preferred form, the surgical drape has a chevron-shaped fenestration for positioning the fenestration relative to the xiphoid process region of a patient, which is useful for establishing the sterile field in certain bariatric procedures. An anesthesia screen at a head of the drape extends laterally to the sides of the base sheet forming the fenestration and defines integral arm board covers. The lateral ends of the anesthesia sheet are sealed in part to close the ends of the arm board covers. A secondary base sheet defining a smaller, secondary fenestration is releasably attached to the base sheet so that the fenestrations can be aligned with one another. Various instrument and chord management features are also included. A method of making the drape is also disclosed.

Abstract: The invention disclosed herein relates to improved elastomeric articles and processes for making the elastomeric articles. In particular, the invention relates to the surface modification of elastomeric articles such as industrial, surgical, and examination gloves that provides for improved consistency with respect to surface tack on a single article, between different articles from a single production batch, and between articles from separate production batches. The surface modification treatment comprises application of an aqueous mixture of silicone emulsion and ammonium salts of alkyl phosphates to the surfaces of elastomeric articles.

Abstract: A surgical mask provides a wide range of wearers with a good fit and improved comfort, facilitates proper use of the mask, and reduces or eliminates fogging of eyewear, as compared with typical masks. The mask may include a pair of ties that are joined to the upper, central, and lower parts of either side of the body of the mask with the assistance of restraint members. The mask may also include a sealing member that reduces or eliminates gaps between the wearer's face and the upper part of the mask by forming a seal between the wearer's face and the mask in use. In addition, the mask may include a barrier panel that reduces or prevents the wearer's breath from escaping through the mask and rising to the wearer's eyewear.

Abstract: A collapsible liner for use in a canister of a medical fluid collection system is disclosed. The liner includes a flexible bag extending longitudinally between a top portion opposite a closed bottom portion, and at least one support element connected to the bag and disposed generally laterally relative to a length of the bag. When an interior of the bag is subjected to a vacuum, the at least one support element limits an extent of lateral collapse while permitting longitudinal collapse.

Abstract: The present invention relates generally to methods of sterilizing elastomeric articles in a manner that prevents and/or reduces degradation to the articles, particularly degradation that may be caused and/or accelerated by sterilization techniques such as gamma irradiation, x-ray irradiation, and electron-beam processing. The methods include packaging the elastomeric articles in order to improve their resistance to degradation. In certain aspects of the invention, packaged elastomeric articles, optionally containing one or more antidegradants, such as antioxidant and/or antiozonant compounds, are also provided. The methods of providing degradation-resistant elastomeric articles in accordance with the present invention may also be used to reduce the occurrence of cracking and discoloration in elastomeric articles, regardless of whether they are subjected to sterilization.

Abstract: The invention disclosed herein relates to an improved process for making elastomeric polyisoprene articles. In particular, the process of the invention is a system which produces synthetic polyisoprene articles exhibiting tensile strength properties similar to that of solvent-based processes using natural rubber latex. The process comprises an accelerator composition at the pre-cure stage comprising a dithiocarbamate, a thiazole and a guanidine compound. In a preferred embodiment, the accelerator composition comprises zinc diethyldithiocarbamate (ZDEC), zinc 2-mercaptobenzothiazole (ZMBT) and diphenyl guanidine (DPG), in conjunction with a stabilizer, such as sodium caseinate. The invention also includes an elastomeric polyisoprene product made by the process, such as a surgeon's glove.

Abstract: Embodiments of the invention provide a suction evacuation system, or smoke evacuation system, for incorporation into hand-held surgical devices. In particular, the system according to embodiments of the invention can be used in hand-held surgical suction-irrigation devices that may also include electrical systems which deliver energy to effect cutting, ablation and coagulation effects at the surgical site. Embodiments of the invention provide a smoke evacuation system that can be incorporated into a hand-held surgical device wherein the smoke evacuation system is structurally and functionally integrated with the suction control system of the device.

Abstract: A method of forming a fenestrated extremity surgical drape includes providing improved seal integrity to reduce the occurrence of pathogenic contamination at the surgical site via migration through the seal. The seal has a non-linear configuration to eliminate uneven stress concentrations commonly located at the corners of rectilinear seals. An elastomeric apertured panel can be disposed between a film panel and a fiber/film laminate panel. These layers can be joined by a heat sealing operation along two spaced apart concentric seal locations ringing the aperture and a fenestration in the laminate panel. The assembly can then be affixed by adhering the underside(s) of one or more panels to a base drape, which has an opening aligned with the aperture and fenestration.

Abstract: An aqueous elastomer dispersion includes a dispersed phase and an aqueous phase. The dispersed phase includes an elastomer including curable aliphatic conjugated-diene elastomers, such as polyisoprene, and a minor amount of at least one additive. The aqueous phase includes water and other optional components in either a soluble state or a dispersion state. The aqueous elastomer dispersion may be prepared by dissolving an elastomer, such as rubber, and additives in a solvent mixture and then converting the resulting solution into an aqueous emulsion. The aqueous emulsion is concentrated and the solvent is stripped from it to yield a dilute latex. The dilute latex that is obtained is concentrated again. Articles made from the aqueous elastomer dispersion include medical gloves, condoms, probe covers, dental dams, finger cots, catheters and the like.

Abstract: An improved protective garment in accordance with the principles of the present invention provides an improved interface between a glove and sleeve of the protective garment. An improved protective garment in accordance with the principles of the present invention is easily incorporated with the protective garment and economically cost effective to implement and use. An improved protective garment in accordance with the principles of the present invention provides an impervious partial sleeve having a surface exhibiting non-adhesive friction when in contact with dry glove materials.

Abstract: There is provided an improved sterilization wrap and a method for using the improved sterilization wrap to sterilize an article. The wrap is made of at least a first panel of sterilization material and includes an additional panel of material. The first panel is multi-layered and includes at least one pathogen filtration layer. The first panel is rectangular and has an outer periphery and a central portion. The outer periphery includes first, second, third and fourth edges. The additional panel of material is bonded to the first panel, approximately at a forty-five degree angle to the first panel, with a substantial portion of the additional panel being adjacent to the central portion of the first panel. The perimeter of the additional panel is smaller than the perimeter of the first panel. Portions of the additional panel are bonded to the first panel along the first, second, third and fourth edges of the first panel.

Abstract: Various embodiments of a fluid collection system having multiple storage chambers are disclosed. In an exemplary embodiment, the system may include a first chamber in fluid communication with a suction source and a second chamber in fluid communication with the first chamber. The second chamber may have a volume less than a volume of the first chamber. The second chamber may also comprise an inlet port for connecting to an external tube. The system may be configured to selectively drain liquid from the second chamber into the first chamber.

Abstract: Various embodiments of a fluid collection system having multiple storage chambers are disclosed. In an exemplary embodiment, the system may include a first chamber in fluid communication with a suction source and a second chamber in fluid communication with the first chamber. The second chamber may have a volume less than a volume of the first chamber. The second chamber may also comprise an inlet port for connecting to an external tube. The system may be configured to selectively drain liquid from the second chamber into the first chamber.

Abstract: Various embodiments of a fluid collection system having multiple storage chambers are disclosed. In an exemplary embodiment, the system may include a first chamber in fluid communication with a suction source and a second chamber in fluid communication with the first chamber. The second chamber may have a volume less than a volume of the first chamber. The second chamber may also comprise an inlet port for connecting to an external tube. The system may be configured to selectively drain liquid from the second chamber into the first chamber.

Abstract: The present invention relates to a method and system for procedure pack inventory management. The system provides access to data relating to healthcare facilities, custom and standard procedure pack data, component data for each procedure pack, and vendor data. The system may filter the access data and output the results of the filterings on a display.

Abstract: A fluid flow control apparatus used in medical fluid sampling. The apparatus includes a valve assembly, first and second ports, and a cap. The valve assembly comprises a body rotatably assembled to a housing and defining a passageway and at least two recesses defined by an interior surface of the housing and the body which is formed separate from the passageway. The ports extend from the housing and are configured for connection to medical devices. The valve assembly is operable to interchangeably align the passageway and the recesses with the ports. Finally, the cap is connected to the housing, and forms an opening for coupling to a specimen container.