Abstract: The present disclosure in one aspect provides a sterile packaging container comprising a container body with a cross-sectional shape that is constant along the majority of the longitudinal axis, a cover and a closure assembly that inhibits the passage of microbial contaminants. The container is configured such that the interior of the container can be sterilized. The sterile packaging container described herein allows one to manufacture a sterile packaging tube exercising the smallest possible volume.

Abstract: A tool box structure includes multiple tool boxes. Each of the tool boxes includes a first case, a second case, a first restriction unit, and a second restriction unit. The first case is provided with a receiving space, multiple first mounting portions, a first locking portion, a first inclined face, two second mounting portions, and a limit portion. The second case is provided with multiple third mounting portions, a second locking portion, a second inclined face, two fourth mounting portions, a first receiving groove, a second receiving groove, and a third receiving groove. The first restriction unit is mounted in the first receiving groove and moved in the first receiving groove to restrict or release the limit portion. The second restriction unit is mounted in the second receiving groove. The second restriction unit is assembled with the first restriction unit.

Abstract: A method for producing a tray for storing aneurysm clips, in which a metal plate is equipped with perforations. The perforations are produced by laser cutting. The plate with the perforations is reshaped by bending to form a corrugated sheet or a sheet with trapezoidal corrugations. The sheet has at least one channel-like indentation for storing aneurysm clips. A tray for storing aneurysm clips includes a corrugated sheet or a sheet with trapezoidal corrugations equipped with laser-cut perforations. The corrugated sheet or sheet with trapezoidal corrugations has at least one channel-like indentation.

Abstract: The present invention relates to a method and system for aseptically filling of flexible packages containing dry cloth. Such a method may include a first stage that is performed in a non-sterile environment. The first stage may include cutting a first substantially dry cloth to a predetermined size; inserting the first cloth into a flexible package; sealing a first end of the flexible package; and sterilizing the flexible package. The method may also include a second stage performed in a sterile environment. The second stage may include filling the flexible package with a medical solution such that the substantially dry cloth absorbs at least a portion of the medical solution; and sealing the open end of the flexible package.

Abstract: The present disclosure includes and provides for methods of packaging medical devices that are to be treated with a fluorinated liquid to alter their surface properties, packaging systems for such medical devices, and methods of utilizing the packaging systems to treat the medical devices. The packaging systems permit effective storage and distribution of medical devices that upon contact with mammalian blood have limited thrombogenicity or are non-thrombogenic and/or are resistant to adhesion of blood cells or clots.

Abstract: A system includes an implant and a packaging device assembled with the implant to hold an outer sleeve and a head element of the implant in a desired position relative to one another. The packaging device includes clip arms sized and shaped so that, when the arms are held toward a closed configuration, the implant is housed therebetween in the desired position and proximal ends of the arms form a space via which an insertion device is insertable to be coupled to the implant, and a housing defining a space within which the clip is housed. The housing includes a retaining feature for retaining the clip therein and a camming element which, when a proximal force is exerted on the implant via the insertion device coupled thereto, causes the arms to move away from one toward an open configuration to release the implant therefrom.

Abstract: A “dry” packaging in which a prosthetic heart valve is packaged within a container with hydrogel that can be provided in many forms. Certain embodiments include hydrogel that is preloaded with glycerol or the like. The hydrogel regulates the humidity within the container through a diffusion-driven mechanism if a gradient of humidity between the inside and the outside of the hydrogel exists. Humidity regulation is important to prevent the tissue of the valve structure from drying out. When the partially-hydrated hydrogel is present within container, which is saturated with air of a predefined humidity, the water molecules from the air will be absorbed by the hydrogel if the air humidity is high (i.e. when the thermodynamics favor hydrogel hydration) or vice versa. Various embodiments are configured to also house at least a portion of a delivery device for delivering the prosthetic heart valve.

Abstract: A drape for an input control console of an elongate device may comprise a main drape section configured to fit over the input control console via a main opening at one end of the main drape section. The drape may also comprise a plurality of pockets. Each of the plurality of pockets may include a pocket opening that is attached to a respective secondary opening in the main drape section. Each of the plurality of pockets may be configured to be anchored, at the pocket opening, to a side surface of a respective raised ring or bezel on the input control console using a respective tightening element.

Abstract: An object transport system includes a plate having an array of apertures; and a plurality of dividers, each of the dividers including an elongate throat connecting a head to a base, wherein the base is arranged to be inserted into one of the apertures.

Abstract: A multifunctional enclosure is described having an elongated sleeve configured with an enlarged opening for the insertion of an elongated member of a medical probe. The multifunctional enclosure is configured to prevent the elongated member of the medical probe from swinging and becoming damaged during transport. The multifunctional enclosure may further comprise an attachment component for securing the medical probe to the multifunctional enclosure. Furthermore, at least one vent may be configured onto the multifunctional enclosure, such as on a first end closure portion. The vent may allow for adequate flow for sterilization and/or drying.

Abstract: A breathable package that allows a device or object disposed in the package to be sterilized, and maintains the sterile condition until the package is opened at the point of use. The package also provides a visual indication that the package seal integrity has not been compromised or that the package has been compromised or breached. The package includes a first material, such as a film, and a second non-woven material, such as non-woven high density polyethylene, that form opposing sides of the package.

Abstract: The blister pack for medicinal products comprises a bottom film in which blister pockets are formed, which are surrounded by webs of the bottom film. The blister pockets comprise a two-level shape with a first recess and second recess situated lower down. A lidding film is sealed to the webs of the bottom film and to a strip of active material, which is arranged in each blister pocket. The medicinal product is accommodated in the second recess, and the strip of active material is accommodated in the first recess. The first recess comprises, in a bottom area thereof, a peripheral rib, which extends around the second recess, or at least two projecting knobs, which are arranged next to the second recess, wherein the strip of active material rests on the rib or on the knobs.

Abstract: Provided is a utility connectivity system. More specifically the presently claimed subject matter is directed to connectivity systems associated with containers and utility units connectable to one another.

Abstract: A tray (100) for accommodating a coiled medical device, such as a catheter assembly (700), includes a first compartment (101), a second compartment (102), and a third compartment (103). The catheter assembly (700) and devices associated with a catheterization procedure, such as syringes (701,702) containing sterile water and lubricating jelly and a specimen container (703) can be disposed within the tray. A first barrier (105) and second barrier (106) separate the compartments. The barriers can have openings (121,122) therein to accommodate large syringes or to enable the first compartment (101) to be used as a lubricant applicator for the catheter. The first compartment (101) can include a stair-stepped contour (115) such that the syringes are held at different depths to facilitate ease of use. The various devices can be disposed within the tray (100) in accordance with their order of use in the catheterization procedure.

Abstract: Apparatus (40) for compressing a transcatheter cardiac stent-valve (10) comprises: a hollow channel (42) having an interior surface (50) shaped for progressively compressing the stent-valve in response to longitudinal advancement of the stent-valve within the channel; a driver (46) threadedly engaged on the exterior of the channel for generating a longitudinal driving force in response to rotation; a mover (44) having limbs (56) that project through slots (58) in the channel wall to transmit the driving force to the stent-valve within the channel; and a channel extension (48) removably attachable at the exit (54) to provide a generally cylindrical containment bore (66).

Abstract: Packaging for a medical device, such as but not limited to an eyelid speculum, is provided. The packaging enables for the shipment, storage, sterilization of the medical device in a secure and efficient manner while also maintaining the sterility of the device post-sterilization and allowing for the easy removal of the medical device from the packaging without compromising the device's sterility.

Abstract: In an aspect, a method of manufacturing a surgical kit includes providing one or more medical devices based on a three-dimensional (3D) image of an anatomical structure. The method additionally includes providing packaging based on the 3D image, and providing the surgical kit utilizing the packaging and the one or more medical devices. In another aspect, a surgical kit has one or more contoured packaging surface having a contour that matches a contour of an anatomical structure. The contoured packaging surface has one or more features for receiving one or more medical devices provided based on the contour in the 3D image. The surgical kit additionally has a lid connected under pressure with the one or more contoured packaging surface. The lid has apertures for sterilization of components of the one or more medical devices situated between the lid and the contoured packaging surface.

Abstract: A drape for a piece of equipment used during a medical procedure may be formed of a flexible sheet of polymeric material. The flexible sheet can have a basin portion shape-indexed to a basin or reservoir of the piece of equipment over which the drape is intended to be draped. The flexible sheet can also have a side sheet portion connected to the basin portion. The side sheet portion can drape down the basin or reservoir of the piece of equipment over which the drape is draped. The basin portion of the flexible sheet can be collapsible. As a result, the drape can be collapsed into planar package for storage. Upon being removed from the package, the basin portion of the drape can be expanded to conform to the walls of the basin of the piece of equipment over which the drape is deployed.

Abstract: An instrument protector backer card provides enhanced structural integrity of a sterile package solution for medical instruments. A mounting surface has a strap for holding a removable medical instrument. A shield member is movable from a non-deployed position into a deployed position to define an open-ended pocket to receive an end of the medical instrument therein. A flap may be used to hold jointed medical instrument in an open position.

Abstract: A method of using a sterilization wrap system including a permeable material having barrier properties and having a first surface and a second opposing surface, the exterior panel being substantially opaque or having a first level of translucence, and an interior panel including a permeable material having barrier properties and having a first surface and a second opposing surface, the interior panel having a level of translucence that is higher than the translucence of the exterior panel, the panels being joined together over at least a portion of their surfaces. Also disclosed is inspection of the sterilization wrap system for exterior panel breaches by looking for light passing through a panel facing the viewer.

Abstract: A product comprising a first compartment and a second compartment. The first compartment has first walls that define a reservoir. The first compartment includes a first lid enclosing a medicament within the reservoir. The second compartment has second walls that define a cavity. The second compartment includes a second lid enclosing a glove within the cavity. The first compartment and the second compartment are coupled together with the reservoir and the cavity separated and sealed from one another. The first walls of the first compartment and the second walls of the second compartment are semi-rigid or rigid.

Abstract: A pre-curved catheter tube of a catheter assembly or other elongate medical device and methods for forming such a device using a heating procedure is disclosed. Pre-curving of the catheter tube is desirable to impart to the catheter assembly a desired positional configuration when the catheter assembly is inserted into a patient. The heating procedure may include heat sterilization procedures commonly used to sterilize medical devices prior to use. One method for curving a catheter tube of a catheter assembly includes constraining the catheter tube into a curved configuration using the tube constraint, heating the catheter tube in the curved configuration for a predetermined time at a predetermined temperature, and releasing the catheter tube from the tube constraint after the heating is complete.

Abstract: Packaging for medical containers, including a tub having a peripheral wall, a sealing cover sealable on an opening of the tub and a sealing envelope able to protect the sealing cover. The sealing envelope includes: a lower sealing part, having a frame able to be sealed to the peripheral wall of the tub, and a bonding surface that extends outwards from the frame, and an upper sealing part sealed on the bonding surface to enclose the opening of the tub and the sealing cover.

Abstract: A roofing underlayment includes a hydrophobic nonwoven core layer that provides enhanced resistance to water infiltration. In addition to the hydrophobic nonwoven core layer, the roofing underlayment includes a coating layer adhered to a surface of the hydrophobic nonwoven core layer, and an exterior surface layer adhered to the coating layer. A roofing system that includes the roofing underlayment is also provided.

Abstract: A sterilizable pouch includes at least one sheet, wherein outer peripheral edges of the at least one sheet are sealed together to define a pouch having an interior space for receiving an article therein. A first releasable seam spans between a first peripheral edge of the at least one sheet to a second, opposite, peripheral edge of the at least one sheet, the first releasable seam dividing the at least one sheet into a first sheet part and a second sheet part. A second releasable seam and a third releasable seam each substantially span from a third peripheral edge of the at least one sheet to a fourth, opposite, peripheral edge of the at least one sheet and along the first peripheral edge and the second peripheral edge, respectively.

Abstract: In some examples, a package includes a package body enclosing a medical supply. The package body defines a window. The package includes a breathable membrane adjacent the package body and extending across the window. The package includes a moisture oxygen scavenger adjacent the package body and extending across the breathable membrane. The package includes an adhesive layer configured to hold the moisture oxygen scavenger adjacent the breathable membrane. In some examples, a technique includes sterilizing a package precursor including the package body and the breathable membrane, and after the sterilizing, adhering the moisture oxygen scavenger to the package body to form the package.

Abstract: The invention includes devices, arrangements and methods for treating an endoscope after use to prevent adhesion of bioburden on internal walls of a lumen of the endoscope. After treatment, the device is stored in the treated condition until cleaning. The device is configured to selectively deliver cleaning solution to the endoscope. The device can be a circulating embodiment having a pump. A filter can be provided to filter debris during circulation. The device can be a non-circulating embodiment having a hydrophobic filter for release of air. Fittings are provided on the device components to selectively attach the device to endoscopes.

Abstract: An expandable and collapsible pouch for accommodating an orthodontic appliance while not is use. The pouch may be selectively and repeatedly coupled to a variety of objects. After selectively coupling the pouch to a desired object, the user opens the pouch by expanding at least one collapsible wall or side. The user then removes their orthodontic appliance, inserts it into the open pouch, and then closes the pouch by letting the pouch contract. When the orthodontic appliance is needed again, the user removes the appliance from the pouch and lets the pouch contract into its original position flush against the surface of the object. The pouch is coupled to the object via a magnet disposed within the pouch that is configured to interact with the surface of the object. The pouch also includes a second magnet which assists the pouch maintain a closed position while an appliance is inserted therein.

Abstract: The invention provides a sterilizable pouch having at least one wall formed of a flexible film and including an opening formed therein for providing communication to an interior space of the package. A breathable material is disposed on an outer surface of the wall covering the opening. The breathable material is joined to the outer surface of the wall with a continuous heat seal. The flexible film forming the wall comprises a multilayer film having a peel feature that permits the breathable material to be peelably removed from the surface of the pouch.

Abstract: A housing according to the embodiment includes a lower surface part, an upper surface part, and a side surface part. The lower surface part includes a contact surface contacting an adherend. The upper surface part is separated in a vertical direction from the lower surface part with a first space interposed. The side surface part is provided around the first space and is connected to the upper surface part and the lower surface part. The upper surface part and the side surface part include a first material. The lower surface part includes a second material that is softer than the first material. A portion that includes the second material is exposed for at least a portion of the contact surface.

Abstract: A food container includes a body having a first and second receptacle. A first food product is contained in the first receptacle. A second food product is contained in the second receptacle. A lid includes two portions coupable to the body, a first portion configured to enclose the first receptacle and a second portion configured to enclose the second receptacle. Each portion has a permeability, and the first portion has a permeability different than the second portion.

Abstract: A system and method utilizing a robotic arm to prepare a food product such as a meat for cooking and then subsequently assembling a sandwich from the cooked meat is disclosed. In addition, the robotic arm may also be used to wrap the assembled sandwich in a wrapper. The system may utilize a wire basket with a basket adapter, or handle, to allow the robotic arm to easily maneuver the basket and also utilize a wrapping assist device to wrap a wrapper around the assembled sandwich.

Abstract: Tattoo removal is disclosed. In an example, a method for removing tattoo ink from skin or resolving a medical condition related to tattoo ink, includes applying a primary solution of beta glucan to a treatment area having tattooed skin. The primary solution stimulates the skin in the treatment area to enhance removal of the tattoo ink from the skin. The example method also includes coating the treatment area with a secondary solution. The secondary solution may have an absorbent material to draw in loose ink. The example method also includes disrupting a skin barrier in the treatment area by a needle or ablative device to improve penetration of at least one of the primary solution and the secondary solution.

Abstract: A packaging system for an elongate tool to be coupled to a surgical device. A segmented packaging body comprises a first distal section, a second distal section, and a proximal section. The first and second distal sections provide a clamshell casing to the distal end of the tool, and the proximal section is pivotally coupled to the first distal section and configured to receive the proximal end of the tool. The packaging body may comprise a living hinge and perforations to facilitate mounting the tool on the surgical device without the user touching the tool, thereby minimizing risk of contamination and/or injury. The proximal section may be detached from the clamshell casing at the perforations after the tool is mounted on the surgical device. Secondary packaging may be provided to receive the packaging body. Methods for mounting the tool disposed within the packaging system are also disclosed.

Abstract: A sterilization process challenge device configured to test the efficacy of a sterilization process includes a tubular body for containing at least one sterilization indicator and a filter assembly including at least one filter member. The only flow path into the interior of the tubular body containing at least one sterilization indicator is provided through the filter assembly to control and restrict flow of a gaseous sterilization medium from an external environment.

Abstract: A method of manufacture and an adhesive patch vent is provided for application to a flexible packaging material. A fabric material has an adhesive applied to its surface. The adhesive being applied to outer portions of the fabric material where a central portion is adhesive free. The adhesive patch vent is applied to an interior of a flexible package material where the adhesive free portion aligns with a perforation in the flexible package material. The adhesive vent patch enables air to be expelled from a package but is resistant to damage to the exterior of the bag. In addition a food grade oil resistant adhesive is utilized.

Abstract: A needle tip assembly for a pre-loaded syringe or a pen needle injection device, including a needle with a first puncturing end projecting from a front side of a needle support and a second puncturing end projecting from a rear side of the needle support. A body sized to receive therein the needle support and the needle. The body including a front portion, a rear portion, and an overall axial length that is greater than an axial length of the needle. Prior to the needle tip assembly being in an installed condition on the pre-loaded syringe or pen needle injection device, the front portion covers the first puncturing end and the rear portion covers the second puncturing end. Prior to removal from the pre-loaded syringe or pen needle injection device, the body is at least axially movable to a position where the front portion covers the first puncturing end.

Abstract: A medical device assembly is disclosed, including a medical device, preferably having a hydrophilic surface coating, and a package accommodating said medical device. The package if formed of two sheets of foil material, a first foil of which has been deep drawn into a trough shape, the package further including a resealable opening arranged within the bounds of the second foil. The medical device may e.g. be a urinary catheter.

Abstract: A filter cassette which is part of a filter system can be fastened to a sterile container lid. The sterile container lid serves to close a sterile container and to make a gas exchange possible between the container exterior and the container interior, without recontaminating the container material. In addition, the filter system fulfils a valve function. In order to center the filter cassette with respect to the sterile container lid, a first centering portion is provided on the filter cassette. The first centering portion interacts with a second centering portion on the sterile container wall section when the filter cassette is inserted into the sterile container lid.

Abstract: In sterile, additive manufacturing wherein one lamella is successively built upon an underlying lamella until an object is completed, a sterile manufacturing environment is provided. A major chamber large enough to accommodate the manufactured object has sterile accordion pleated sidewalls and a sterile top closed with flap valves. A minor chamber for supporting the nozzles positioned above the major chamber has similar valves in corresponding positions. Nozzles for material deposition penetrate the pair of valves to block air and particles from entry into the major chamber where the nozzles make layer by layer deposition of the object using XY areawise nozzle motion relative to the object as well as Z nozzle vertical motion with the major chamber expanding as the object is formed.

Abstract: A sterilization wrap system with features for protecting a sterilization wrap and/or a sterilization tray of the sterilization wrap system is provided. Such features include strap or belt protectors, edge protectors, corner protectors, and/or expandable protectors, which each may provide protection of one or more areas of the sterilization wrap and/or tray when positioned against an outer surface of the wrap and/or between an inner surface of the wrap and a container for holding implements to be sterilized. A size-selectable protection system also is provided. The size-selectable protection system provides a material having a plurality of perforations such that a length of the material may be selected and detached from the rest of the material. The selected length of material may be used with a sterilization wrap system to protect a sterilization wrap and/or sterilization tray from cuts, tears, or the like.

Abstract: A sterilization container for retaining surgical instruments in a sterilizer comprising a plurality of walls defining an interior volume sized to receive at least one instrument tray, least one of the walls defining a venting pass through area, and a filter occluding the venting passage area, wherein a ratio of the venting pass through area to the interior volume is at least 1 square inch:125 cubic inches.

Abstract: The invention relates to a system for containing medical waste with a bag and a machine for producing said bag. It relates to a reusable, hermetically sealed, metal container for medical waste, with a bag and locks or latches, which prevent the lid from being opened until the waste inside the same has been sterilized by the pressurized steam of an autoclave. It also relates to said plastic bag made up of two or more layers of different physical properties, configured into a single body. Said bag is housed inside the aforementioned hermetically sealed container. It also relates to a machine for producing these bags with a winder, folder and several sealers using heat resistance inserted into conveyer belts.

Abstract: A method of preparing a ready-to-use catheter by providing a catheter assembly that has a first compartment that includes a catheter therein. The catheter includes on at least a part of its surface an exterior coating designed to reduce the coefficient of friction after treatment with a liquid swelling medium, and a second compartment containing a liquid swelling medium. The method includes sterilising the catheter assembly, adding the liquid swelling medium to the first compartment for wetting/activating the exterior coating of the catheter, and storing the ready-to-use catheter. By using the method according to the invention, the sterilisation of the catheter is effectuated in a dry-state, ensuring that the known problems with wet-sterilisation are completely eliminated and the need for preparing complicated and expensive liquid swelling mediums are no longer required.

Abstract: The present disclosure, in one embodiment, relates to a packaging assembly for holding liquids, viscous material, or particulate material. The packaging assembly includes a carton having side and bottom walls and an open top. A self-supporting plastic liner fits inside of the carton and is for containing liquids, viscous material, or particulate material. The liner has a side wall, a closed bottom end, and an open top end having an outwardly-projecting rim. The rim has a radially-extending flange portion, and a dependent skirt portion. When the self-supporting plastic liner is inside of the carton, the dependent skirt portion of the rim hangs over the side walls of the carton. A lidding material is removeably affixed to the rim of the plastic liner. A carton lid closes off the open top of the carton.

Abstract: A sleeve kit comprising a container sleeve and a sleeve cap which may be engaged with the container sleeve to form a sleeve assembly that envelopes a slush container, the sleeve kit including an attachment system to allow the sleeve cap to be engaged with the container sleeve to form the sleeve assembly and then become disengaged so that the slush container may be removed from the container sleeve. The attachment system may be a single-use attachment system to allow the sleeve cap to be engaged with the container sleeve to form the sleeve assembly. The container sleeve may have a set of at least one vent which allows air to move from an open top end of the container sleeve to a space between a bottom of an inserted slush container and a bottom of the container sleeve to facilitate removal of the slush container from the container sleeve.

Abstract: A delivery system package includes a tray, a delivery system, and a slip card between the tray and the delivery system. To remove the delivery system, a pull tab of the slip card is moved to raise the slip card including the delivery system from the tray. At the same time, this moves the slip card over a lid sealing flange of the tray, considered a non-sterile surface in accordance one embodiment. Accordingly, the slip card extends over the lid sealing flange preventing contact between the delivery system and the lid sealing flange. In addition, the slip card effectively forms a ramp for sterile removal of the delivery system from the tray.

Abstract: Disclosed herein are embodiments of a valve assembly for preventing dead leg spaces in a container or tubing, the embodiments including a three-way valve system for controlling back-pressure in a fluid generating device, such as a single-use high pressure bioreactor. Also disclosed is a pressurized reactor system for bioprocessing, comprising a single-use container including a flexible wall or a semi-rigid wall.

Abstract: The package (1) for a surgical mesh (100) comprises: a receiving member (2) configured and dimensioned to receive at least one surgical mesh (100), and a covering member (3) configured and dimensioned to cover the said at least one surgical mesh (100) maintaining with the receiving member (2) the surgical mesh (100) in a substantially flat position, and a gas channelling network interposed between the said receiving member (2) and the said covering member (3) configured to channel a sterilization gas within the at least one surgical mesh (100).

Abstract: A sterilization container for retaining surgical instruments in a sterilizer comprising a plurality of walls defining an interior volume sized to receive at least one instrument tray, least one of the walls defining a venting pass through area, and a filter occluding the venting passage area, wherein a ratio of the venting pass through area to the interior volume is at least 1 square inch:125 cubic inches.