Abstract: A suturing device includes a body configured to be inserted into a surgical site of a patient. A suture retainer is positioned within the body and configured to receive a suture so that an end of the suture extends from the body and is accessible within the surgical site of the patient.

Abstract: Storage device for a guide wire or dilation balloon including a tank, and a frame including two walls forming between them an internal volume and including an insertion aperture. The frame includes an opening passing through the frame from one wall to the other, and a slot formed in the internal volume and communicating with the insertion aperture, the slot opening into the opening over part of its perimeter, referred to as open part. The tank includes a positioner configured to place the frame in a stowage position in which the open part of the slot is situated at least partly inside the tank and the insertion aperture extends outside the tank, the tank further including a stop configured to block the translational movement of the frame in directions of insertion and extraction of the guide wire or of the dilation balloon into and out of the frame.

Abstract: An organization device for maintaining a suspensory graft fixation device (i.e., an implant and suture) in a desired position. The device includes a substrate having top and bottom edges with first and second panels extending therebetween. The device also includes a first central longitudinal axis extending in a direction from the top edge to the bottom edge between the first and second panels. The first and second panels are foldable about the axis between open and closed positions. The device also includes an opening extending through the bottom edge and into the first panel, and a plurality of top slits and bottom slits. The plurality of top slits includes at least one top slit which is aligned with the first opening. The device additionally includes a tabs adjacent the opening. The slits and tabs are configured to maintain suture of a suspensory graft fixation device in an organized manner.

Abstract: A method of suturing an abdominal cavity includes inserting a spool of suture in the abdominal cavity. The method also includes capturing a first portion of the suture and removing the first portion from the abdominal cavity. The method also includes capturing a second portion of the suture and removing the second portion from the abdominal cavity. The method also includes tying the first portion to the second portion outside of the abdominal cavity.

Abstract: An organization device for maintaining a suspensory graft fixation device (i.e., an implant and suture) in a desired position. The device includes a substrate having top and bottom edges with first and second panels extending therebetween. The device also includes a first central longitudinal axis extending in a direction from the top edge to the bottom edge between the first and second panels. The first and second panels are foldable about the axis between open and closed positions. The device also includes an opening extending through the bottom edge and into the first panel, and a plurality of top slits and bottom slits. The plurality of top slits includes at least one top slit which is aligned with the first opening. The device additionally includes a tabs adjacent the opening. The slits and tabs are configured to maintain suture of a suspensory graft fixation device in an organized manner.

Abstract: Synthetic chord devices and methods for using the same for connecting tissues are provided. Aspects of the synthetic chord device include a flexible cord having an attachment element at both a first and a second end, wherein each attachment element includes a piercing member coupled to a securing member that attaches the flexible cord to a first tissue. At least a portion of the flexible cord can be configured to be secured to a second tissue. Aspects of the invention also include sets of the synthetic chord device with pre-measured flexible cords. The devices and methods of the invention find use in a variety of applications, such as in applications in which it is desired to repair a heart valve.

Abstract: A convertible sawhorse and worktable including a sawhorse assembly having first and second outer-facing side surfaces and a worktable top assembly arranged for selectable positioning relative to the sawhorse assembly, the worktable top assembly including a worktable surface defining element and a worktable auxiliary support assembly, the worktable top assembly having at least two operative orientations including a storage operative orientation wherein the worktable surface defining element is located adjacent the first outer-facing side surface of the sawhorse assembly and the worktable auxiliary support assembly is located adjacent the second outer-facing side surface of the sawhorse assembly and a worktable usage operative orientation wherein the worktable surface defining element is located above the sawhorse assembly and the worktable auxiliary support assembly is located adjacent the second outer-facing side surface of the sawhorse assembly.

Abstract: Systems and methods for preparing a ligament graft for a ligament reconstruction procedure are provided. In general, the described techniques utilize a graft holder construct having a graft preparation holder and a suture assembly removably coupled thereto. The graft preparation holder includes an elongate support rail having a longitudinal axis, and a plurality of leaf segments positioned along the longitudinal axis in a spaced relationship and extending laterally from the support rail. The leaf segments can bend to a graft holding configuration so as to define a graft receiving channel configured to receive a graft therethrough. The holder also has at least one support structure configured to mate with the leaf segments to provide stability and rigidity to the segments. The suture assembly has at least one suture tail that can be pulled to affix the suture assembly to a graft without penetrating the graft.

Abstract: A packaging, in particular sterile packaging, for a medical product, includes a receiving space for the medical product. A portion of the packaging facing the receiving space is made at least in part, preferably entirely, of a resorbable material.

Abstract: Medical packaging for the sterile storage of medical articles in a hermetically and sterile sealable packaging sleeve. The packing generally includes at least two parts, with a sealed, film-like outer packaging, which at least partially encloses the packaging sleeve in a form-fitting manner and provides a pressure that is reduced with respect to the atmosphere. At least one end face of the packaging sleeve may be designed to be flattened, wherein a length of the outer packaging is generally longer than a length of the packaging sleeve and projects beyond the end face region of the packaging sleeve. A sealing or welding seam may be arranged at least in the end face region of the packaging sleeve, wherein at least one of the end faces of the packaging sleeve, preferably both end faces, are designed so as to be flattened off. The end-sided transition from the packaging sleeve into the outer packaging is substantially wrinkle free.

Abstract: A split case assembly for a gas turbine engine includes an outer diameter case defining a partial case structure for a gas turbine engine and multiple fixed-variable vanes attached to an inner diameter surface of the outer diameter case. Each of the fixed-variable vanes protrudes radially inward from the outer diameter case. Each of the fixed-variable vanes in the plurality of fixed-variable vanes is interfaced with one of a plurality of inner diameter boxes at a radially inward end of the fixed-variable vane, such that the inner diameter boxes define an inner diameter of a flow path and the outer diameter case defines an outer diameter flow path. Each of the fixed-variable vanes are interfaced with the one of the plurality of inner diameter boxes through at least one inner diameter shoe in a plurality of inner diameter shoes.

Abstract: A system for aligning a needle driver with a tip of a suture needle includes a suture needle package having a base, a needle driver alignment guide, and at least one connector for securing the suture needle. The needle driver alignment guide has first and second lateral guide walls that oppose one another for defining a needle driver guide channel. An end wall interconnects the first and second lateral guide walls for defining a distal end of the needle driver alignment guide. The at least one connector secures the suture needle over the base and controls the orientation of the suture needle so that a tip of the suture needle is located within the suture needle guide channel and is bounded by the end wall and the first and second lateral guide walls. A needle driver has a clamping assembly at a distal end that engages the end wall of the needle driver alignment guide for aligning the clamping assembly with the tip of the suture needle.

Abstract: A suture retainer is provided for supplying a surgical needle and an associated length of relatively stiff suture material to a surgical suturing apparatus. The suture retainer generally includes a body portion defining a suture tray and a loading unit positioned on the body portion. The loading unit is provided to retain a surgical needle in a position to be grasped by a surgical suturing apparatus. The suture tray retains the length of relatively stiff suture in a manner which prevents the relatively stiff suture from bending or otherwise being deformed.

Abstract: A container is described for storing various tools and items for sewing in an organized manner and facilitating the process of sewing (e.g., for sewn in hair extensions) for example, by distributing thread. In an example embodiment, the introduced container comprises a housing within which one or more spools of thread can be stored on one or more spindles. The housing can be enclosed by a container top that includes a threading hole through which thread from the one or more spools can be extracted from the interior of the housing, while in use. Further, the container top can include a pin and/or needle holder such as a pin cushion. The container may include additional features such as a bracket for holding a pair of scissors and a drawer for stowing extra thread and/or needles.

Abstract: A break-open single-dose sealed package and method for the production thereof; the sealed package has: a first sheet of semi-rigid plastic material; a second sheet of flexible plastic material set on top of and welded to the first sheet along an annular weld, so as to define a sealed pocket containing a dose of a product; and a pre-weakened area that develops transversely and is obtained in a central area of the first sheet; the pocket is divided into two distinct and separated chambers which are insulated from one another and each contain a corresponding component of the product; and the pocket is divided into the two chambers due to a central weld connecting the second sheet to the first sheet and is weak, so as to be broken by exerting pressure on at least one of the two chambers.

Abstract: A universal sterile packaging assembly for an orthopedic device includes an outer blister having a first recessed central region and an inner blister having a second recessed central region. The second recessed central region includes a protrusion configured for securement of a medical part thereto. The inner blister is sized to fit within the first recessed central region. The assembly also includes a first lid securable to the inner blister and a second lid securable to the outer blister so as to enclose the inner blister within the outer blister.

Abstract: A suturing kit includes a suture and a suture holder for holding the suture. The suture has a first end and a second, opposite, end. The suture holder includes an elongated wall defining a suture receiving passage that is elongated along a longitudinal axis and terminates at a suture exit opening. The suture receiving passage has a width at least twice the diameter of the suture and receives the suture such that the suture is folded over forming a half loop section spaced from the suture exit opening. A first second of the suture extends from the half loop section toward the first end and a second section of the suture extends from the half loop section towards the second end. The first section and the second section of the suture within the suture receiving passage are aligned parallel to the longitudinal axis.

Abstract: A package for surgical sutures has a base member, an outer wall extending upwardly form the periphery of the base member, a plurality of pyramidal shaped standoff members arranged in an oval shape and a flat suture channel cover member having a plurality of precision holes to lock the cover member to the standoff members of the base member. The inner surface of the outer wall of the base member is a profiled surface and the outer periphery of the cover member has a profiled surface corresponding to the profiled surface of the outer wall of the base member. The profiled surface of the outer wall can consist of a plurality of D shaped vertical members extending from the top surface of the base member to the top of the outer wall.

Abstract: The present invention relates to a process for sterilizing implantable biomaterials. In particular, the invention relates to a process for sterilizing collagen-containing implantable biomaterials and storage thereafter.

Abstract: A variety of configurations of implant management devices are provided. The configurations provide different combinations of features for maintaining a location of an implant with respect to the device and managing filaments of the implant. One exemplary embodiment of a device includes a generally rectangular-shaped body having an implantable body retainer, an opening disposed a distance apart from the retainer and configured to receive a ligament graft therein, and a fold extending across the body and intersecting the opening. Folding one end of the body towards a bottom surface of the body along the fold can form a filament loop engaging region to hold in tension a filament loop extending from the implant. Additional filament(s) associated with the implant can be managed by various filament retention features. Methods for preparing a ligament graft for implantation by relying upon indicia formed on a surface of the device body are also provided.

Abstract: In some examples, a medical device package may include a backing card that is configured to secure a medical device to a major surface of the backing card. The backing card is configured to be assembled from an open state into a closed state in which flaps on one or more ends of a central region of the backing card move over some of the central region and cover some of the secured medical device. The closed state defines a reduced footprint relative to the unfolded state. The backing card may be sealed in a pouch, which may then be housed in a carton. The carton includes exterior walls that enclose the sealed backing card and spacing elements that receive the sealed backing card at a relative location within the carton and holds the backing card a threshold distance from the exterior walls of the carton.

Abstract: Materials and methods for immobilizing bioactive molecules, stem and other precursor cells, and other agents of therapeutic value in surgical sutures and other tissue scaffold devices are described herein. Broadly drawn to the integration and incorporation of bioactive materials into suture constructs, tissue scaffolds and medical devices, the present invention has particular utility in the development of novel systems that enable medical personnel performing surgical and other medical procedures to utilize and subsequently reintroduce bioactive materials extracted from a patient (or their allogenic equivalents) to a wound or target surgical site.

Abstract: A method of treating a tubular medical device with a biomolecule comprises the steps of: a) providing a polyolefin tubular substrate forming a tubular medical device; b) cleaning the tubular polyolefin substrate; c) exposing the tubular polyolefin substrate to a reactive gas containing at least one of acrylic acid and siloxane and to plasma energy to yield a plasma-deposited coating on at least one surface of the tubular polyolefin substrate; and d) attaching a biomolecule to the polyolefin substrate following formation of the plasma-deposited coating on at least one surface of the tubular polyolefin substrate, and wherein the biomolecule is at least one of an antibacterial agent, antimicrobial agent, anticoagulant, heparin, antithrombotic agent, platelet agent, anti-inflammatory, enzyme, catalyst, hormone, growth factor, drug, vitamin, antibody, antigen, protein, nucleic acid, dye, a DNA segment, an RNA segment, protein, and peptide.

Abstract: A variety of configurations of implant management devices are provided. The configurations provide different combinations of features for maintaining a location of an implant with respect to the device and managing filaments of the implant. One exemplary embodiment of a device includes a generally rectangular-shaped body having an implantable body retainer, an opening disposed a distance apart from the retainer and configured to receive a ligament graft therein, and a fold extending across the body and intersecting the opening. Folding one end of the body towards a bottom surface of the body along the fold can form a filament loop engaging region to hold in tension a filament loop extending from the implant. Additional filament(s) associated with the implant can be managed by various filament retention features. Methods for preparing a ligament graft for implantation by relying upon indicia formed on a surface of the device body are also provided.

Abstract: The invention relates to a support base (1?) for a suture thread having two opposite sides (12, 14) and comprising on one side (12) thereof a storage channel (2) for a suture thread in a wound position, and a holding zone (4) of one end of the suture thread, the holding zone (4) being surrounded by the storage channel (2), the support base (1) being characterized by having a through-opening (5) between the two sides (12, 14) thereof, the through-opening (5) extending into the holding zone (4) and continuing from the holding zone (4) in such a way as to intersect the storage channel (2), and a shutter (8) moving between an open position for uncovering the through-opening (5) between the two sides (12, 14) thereof, and a closed position for at least partially opening the through-opening (5), the moving shutter (8) being configured to project, in the open position thereof, from the side (14) of the base (1?) which is opposite to the side (12) on which the storage channel (2) is formed.

Abstract: An accommodation tool is disclosed with which an operator can easily wind and accommodate a flexible medical elongated body. An accommodation tool winds and accommodates the flexible medical elongated body, for example, a guide wire. The accommodation tool has an inner wall, an outer wall, and an interlock wall. The guide wire is wound around the inner wall. The outer wall defines an accommodation space for accommodating the guide wire between the inner wall and the outer wall, and that is disposed further outward in a radial direction from a centroid of the accommodation tool than the inner wall. The interlock wall interlocks one end portion of the inner wall and one end portion of the outer wall with each other.

Abstract: A container lid with a finger entry section, a thumb entry section, a grasping section, and a mating section. The finger entry section includes a finger opening for receiving at least one finger of a hand. The thumb entry section includes a thumb opening for receiving a thumb of the hand. The grasping section is coupled to the finger entry section and the thumb entry section. The grasping section functions to grasp an item when compressed via the finger entry section and the thumb entry section and collectively prevent the finger(s) and the thumb from making direct contact with the item. The mating section is coupled to the finger entry section, the thumb entry section, and/or the grasping section and functions to mate the container lid with a container body.

Abstract: A gift card folder for securing a gift card is described. The gift card folder may be composed of a single sheet of substantially rectangular stationary which has a plurality of creases dividing the single sheet of stationary into panels of which two panels cooperate together to form a pop-up shelf upon manipulation of the gift card folder. A portion of the pop-up shelf comprises one or more slits to secure the gift card in a fixed position during opening or closing of the gift card folder. Further, the gift card folder may optionally include a flap that cooperates with an outer panel to secure the gift card folder in a closed position which compresses the pop-up shelf. When the recipient opens the folder, the gift card folder projects the pop-up shelf outward and towards the recipient of the gift card.

Abstract: A package for a medical device includes a folder having bottom and top panels, the bottom panel including a leading edge, a trailing edge, and at least one medical device securing element. The top panel has a leading edge, and a trailing edge joined with the trailing edge of the bottom panel. The folder has an unfolded configuration in which the leading edges of the top and bottom panels face in opposite directions, and a folded configuration in which the top panel is folded over the bottom panel so that the leading edges of the top and bottom panels face in the same direction and are aligned with one another. The folder is insertable into a sealable pouch having a seal with a first leg whereby the leading edges of the folder are abutted against the first leg of the seal of the pouch.

Abstract: A suture anchor cartridge having a rectangular case portion that includes a top portion and a rectangular bottom portion, the bottom portion including an opening, and the top portion being slidably connected with the bottom portion. A suture anchor is suspended in the opening in the bottom portion. The suture anchor being held at a distal end and at a proximal end by the suture anchor cartridge, and a suture-threading loop is disposed within the bottom portion.

Abstract: A suture delivery tool releasably secures a self-retaining suture to permit delivery of the self-retaining suture to a surgical site in a patient through an access port. Suture delivery tools are disclosed suitable for manual operation and operation using robotically-assisted surgical systems. In some embodiments, a suture spool is part of a cartridge which is releasably attached to the suture delivery tool. Cartridges is, in some embodiments, replaced after deployment of the self-retaining suture and different cartridges having different self-retaining suture are, in some embodiments, selected and attached to the suture delivery tool as required for a procedure.

Abstract: A suture retainer is provided for supplying a surgical needle and an associated length of relatively stiff suture material to a surgical suturing apparatus. The suture retainer generally includes a body portion defining a suture tray and a loading unit positioned on the body portion. The loading unit is provided to retain a surgical needle in a position to be grasped by a surgical suturing apparatus. The suture tray retains the length of relatively stiff suture in a manner which prevents the relatively stiff suture from bending or otherwise being deformed.

Abstract: An apparatus and a method for surgical suturing with thread management. An illustrative apparatus for tissue suturing includes a cartridge having a suturing needle having a pointed end and a blunt end, the suturing needle capable of rotating about an axis, a reciprocating needle drive, and an actuator capable of releasably engaging the needle drive to rotate the needle. A method for suturing tissue is provided that includes placing a suturing device having a cartridge containing a suturing needle to span at least one tissue segment, activating an actuator to cause rotational movement of the suturing needle through the at least one tissue segment, and deactivating the actuator to stop an advancing movement of the suturing needle to cause a suturing material to be pulled through the at least one separated tissue segment forming a stitch.

Abstract: A variety of medical devices including staples sutures and dental floss with surface treatment on at least one tissue-facing surface to improve biologic function such as to control tissue adhesion are disclosed including heparin surface treatment which provides heparin present in an amount to yield heparin bioactivity of at least one of i) an ATIII binding of at least 2 pmol/cm2, and ii) a thrombin deactivation of at least 0.2 IU/cm2; an acrylic surface treatment for coupling thereto of a heparin surface treatment, a collagen surface treatment or both; and an amino-functional polysiloxane surface treatment for coupling thereto of a heparin surface treatment.

Abstract: A method of manufacturing an end effector assembly including first and second energizable portions configured to supply energy to tissue is provided. The method includes forming a substrate including first and second portions interconnected by a connector portion. The substrate is formed as a single integrated component. The method further includes engaging the substrate with an insulative member, and removing the connector portion of the substrate to electrically insulate the first and second portions from one another.

Abstract: Devices, systems, and methods are provided for managing suture filaments when performing soft tissue repair. One exemplary embodiment of a surgical suture management device is in the form of a suture loop management card. The card can generally be configured to hold open a collapsible loop of suture until a force applied to the loop is greater than a threshold tension. The card can include a number of different features that help to keep the loop open until the threshold tension is achieved, including features designed to prevent the filament from being mistakenly offloaded. The card can be configured to be removably inserted into a handle of an inserter tool for use as a surgical tissue repair system. Other devices, systems, and methods for performing soft tissue repair are also provided.

Abstract: A method of making a packaged antimicrobial suture having improved shelf life. The method comprising the steps of providing an inner package having a source of antimicrobial agent, providing an adsorbent material effective to adsorb a portion of the antimicrobial agent over time, positioning a suture within the inner package, the suture comprising one or more surfaces, covering the inner package with an outer package having an inner surface and subjecting the suture, the inner package and the inner surface of the outer package to time, temperature and pressure conditions sufficient to vapor transfer an effective amount of the antimicrobial agent from the antimicrobial agent source to the suture and the inner package, thereby substantially inhibiting bacterial colonization on the suture and the inner package, wherein the packaged antimicrobial suture exhibits improved shelf life.

Abstract: A cartridge for holding a suture anchor having a body, including a holder assembly adapted to releasably hold at least one suture anchor, the body having a proximal face, a passage extending from the proximal face of the body to the holder assembly, and a spool adapted to releasably wind a portion of a suture therearound is provided. A kit, including at least one suture anchor, a cartridge for holding the at least one suture anchor, and a suture may also be provided.

Abstract: An instrument for passing sutures in tissue repair and/or other mini-open procedures. The instrument includes a pair of jaws mounted on a distal end of a shaft, a hand assembly mounted on a proximal end of the shaft, and a needle mounted on the hand assembly and through a cannulation of the shaft. The pair of jaws includes a lower jaw and an upper jaw, the lower jaw being provided with a slot configured to engage a plurality of sutures. The hand assembly has a finger lever with a ratchet and a releaser with a hook, the hand assembly being designed to move the needle from a first position to a second position, and to sequentially engage the needle with each of the plurality of sutures.

Abstract: A wound closure assembly and method for its use. The wound closure assembly includes a curved inserter having a distal end and a proximal end, a filamentary element extending between a proximal end and a distal end, wherein the proximal end is coupled to the proximal end of the curved inserter, a first anchor coupled to the filamentary element between its first and second ends, and a second anchor positioned at the distal end of the filamentary element. The filamentary element is configured to form a slip knot between the first and second anchors so as to enable the distance between the first and second anchors to be decreased by pulling on the proximal end of the filamentary element. The distal end of the curved inserter is received within a channel in the first anchor that extends along its longitudinal length.

Abstract: A multicompartment envelope or sterilization receptacle for receiving and storing medical instruments includes an adhesive flap for sealing multiple compartments within a single envelope. Individual compartments within the multicompartment enveloped can be opened while still keeping the seal of other compartments, thus keeping unused instruments sterilized. The multicompartment envelope or sterilization receptacle has an aperture for insertion of a heat-deforming color changing sterilization indicator device, where, after exposure to extreme heat, the sterilization indicator device deforms and cannot thereafter be inserted or removed from an aperture of a sterilization receptacle fitted for an unsterilized sterilization indicator device. Thus, the practitioner is assured of sterilized instruments in a sterilization receptacle, when an intact, color changed sterilization indicator device is within the aperture of the sterilization receptacle.

Abstract: A method of making a packaged antimicrobial suture comprising the steps of providing a containment compartment that is substantially free of an antimicrobial agent; positioning a suture within the containment compartment, said suture comprising one or more surfaces having an antimicrobial agent disposed thereon, said antimicrobial agent being selected from the group consisting of halogenated hydroxyl ethers, acyloxydiphenyl ethers, and combinations thereof; placing the containment compartment having the suture in an outer package; and subjecting the outer package, the containment compartment and the suture to time, temperature and pressure conditions sufficient to transfer an effective amount of the antimicrobial agent from the suture to the containment compartment, while retaining an effective amount of said antimicrobial agent on the suture, thereby substantially inhibiting bacterial colonization on the suture and the containment compartment.

Abstract: A sensor kit comprising a sensor for detecting an analyte, a sensor housing and a calibration chamber. The calibration chamber comprises a first compartment containing a first calibration solution and a second compartment containing a source of the analyte to be detected. A dividing material is located between the first and second compartments enabling them to be mixed on breakage or removal of the dividing material. Further compartment(s) containing further source(s) of the analyte may optionally be provided. Calibration can carried out by (a) taking a reading of the analyte concentration of the first calibration solution, (b) mixing the contents of the first and second compartments by breaking or removing the dividing material, and (c) taking a reading of the analyte concentration of the resulting mixture. Steps (b) and (c) can be repeated for further compartment(s) to provide further reading(s) if desired.

Abstract: A method of identifying the orientation of a tissue sample is provided. The method includes the use of a single-use tissue marking system for use in marking a tissue sample. A first surface of the sample is marked with a first ink defined by a first color; a second surface of the tissue is marked with a second ink defined by a second color; and a third surface of the sample is marked with a third ink defined by a third color.

Abstract: Various embodiments of suture packages are disclosed to provide a surgical needle, having an associated length of suture material, to a surgical suturing instrument. The disclosed suture packages generally include a body portion having a needle supplying loading unit mounted thereon. Various methods of affixing the loading unit to the body portion are disclosed. The body portion defines a suture tray and a cover is provided to secure a suture within the suture tray. A securing ring is provided to secure the cover to the body portion.

Abstract: A urinary catheter kit is provided. The catheter kit includes a catheter with a flared end and a package provided with interior protrusions for cooperating with the flared end of the catheter. The largest outer diameter of the flared end of the catheter is slightly larger than the smallest diameter of the package at the protrusions. Thereby, the protrusions will function as a backstop for the catheter. The rigidity of the catheter at the flared end is selected so that—depending on the angle of the flared end—the flared end will be able to flip over if it is subjected to a force over a predetermined level. Thereby the catheter will be able to be entered back into the package.

Abstract: The present disclosure provides a medical device package including a container for receiving a medical device having an area configured for storing at least one agent and a port for permitting the passage of a contact material between the outside the container and the area configured for storing the agent.

Abstract: A method of making a packaged antimicrobial suture. The method includes the steps of providing a containment compartment molded from a polymeric resin comprising a polymeric material and an antimicrobial agent, positioning a suture within the containment compartment, the suture comprising one or more surfaces; covering the containment compartment having the suture in an outer package cover having an inner surface, and subjecting the outer package, the containment compartment and the suture to time, temperature and pressure conditions sufficient to vapor transfer an effective amount of the antimicrobial agent from the containment compartment to the suture, while retaining an effective amount of the antimicrobial agent on the containment compartment, thereby substantially inhibiting bacterial colonization on the suture and the containment compartment. A packaged antimicrobial suture is also provided.

Abstract: The present invention relates to bags made from medical-grade paper for sterilization, with sterilization-process indicators and pigmented-adhesive-based safety features, which is easy to handle and use and can be used to store materials, more particularly surgical medical material, for sterilization. Such bags are produced using medical-grade paper that is treated on the surface thereof with a microbiocide for sterilization, and, owing to the structure and design thereof, allow safe, rapid handling of the sterilized material placed within, since there are visual indicators that guarantee the hermetic closure and sealing thereof. Furthermore, generally, the invention has printed indicators that change color depending on the sterilization process carried out on the bags and on whether said process was carried out correctly.

Abstract: The invention relates to a device for storing and classifying at least one surgical suturing thread (3) fitted on a needle (30). This device is noteworthy in that it comprises a support (1), of which at least one part of one of the faces (11), called ‘top’ face, supports removable means (2) of fixing said thread (3), and in that said support (1) comprises means (5, 5?) of displaying technical characteristics specific to each suturing thread (30) and/or to each needle (30) to be stored. Applicable to the medical domain.