Package for Medical Devices Including a Pinch-Open Closure

Abstract

A package includes a flexible body configured to transition between a collapsed configuration and an expanded configuration. The body includes an open first end, a closed second end, and sides extending between the first end and the second end. The package also includes a closure connected to the body having a first end, a second end, and a slit extending at least partially between the first end and the second end of the closure. The closure is configured to transition between a closed configuration, in which the closure retains the body in the collapsed configuration sealing the open first end of the body, and an open configuration upon application of a biaxial force to the first end and the second end of the closure, which causes the body to transition to the expanded configuration.

Claims

1. A package for at least one medical device comprising a vascular access device, a disposable syringe, and/or a prefilled syringe, the package comprising: a flexible body configured to contain the at least one medical device and to transition between a collapsed configuration and an expanded configuration, the body comprising an open first end, a closed second end, and sides extending between the first end and the second end; and a closure connected to the body comprising a first end, a second end, and at least one slit extending at least partially between the first end and the second end of the closure, wherein the closure is configured to transition between a closed configuration, in which the closure retains the body in the collapsed configuration sealing the open first end of the body and preventing removal of the at least one medical device from the flexible body through the open first end, and an open configuration, which permits removal of the at least one medical device from the flexible body through the opened at least one slit of the closure, upon application of a biaxial force to the first end and the second end of the closure, which causes the body to transition to the expanded configuration.

2. The package of claim 1, wherein an outer periphery of the closure is an ellipse or a rectangle.

3. The package of claim 1, wherein, when in the open configuration, the closure defines a square, rectangular, or parallelogram shaped opening, and wherein, once moved to the open configuration, the closure remains in the open configuration when the application of the biaxial force ceases.

4-5. (canceled)

6. The package of claim 1, wherein the body comprises polyethylene terephthalate, polypropylene, low-density polyethylene, or combinations thereof, and wherein the closure comprises a plastic strip comprising polypropylene, high density polyethylene, or combinations thereof.

7. The package of claim 1, wherein the body comprises a first sheet and a second sheet of a flexible polymer material sealed together about portions of a periphery of the first sheet and the second sheet, thereby forming the open first end, the closed second end, and the sides of the body.

8. The package of claim 7, further comprising a coating comprising vinyl acetate over exterior surfaces of the first sheet and/or the second sheet of the body.

9. The package of claim 1, wherein, when the closure is in the closed configuration, the at least one slit of the closure is sealed, thereby sealing the open first end of the body, and wherein the application of the biaxial force to the first end and the second end of the closure unseals the at least one slit, thereby allowing the sides of the closure to move apart causing the body to move to the expanded configuration.

10. The package of claim 1, wherein the first end of the closure comprises a first living hinge and the second end of the closure comprises a second living hinge.

11. The package of claim 10, wherein the closure further comprises a first side part extending between the first living hinge and the second living hinge, and a second side part extending between the first living hinge and the second living hinge, and wherein the first side part and the second side part are separated by the at least one slit.

12. The package of claim 11, wherein the first side part comprises a first weakened buckling portion and the second side part comprises a second weakened buckling portions, and wherein the buckling portions are configured to bend as the closure moves from the closed configuration to the open configuration.

13. The package of claim 12, wherein a width of the buckling portions is less than a width of other portions of the first side part and the second side part, and wherein the closure is an integrally molded part comprising the first side part and the second side part connected by the first living hinge and the second living hinge.

14. (canceled)

15. The package of claim 1, wherein the closure and the first open end of the body are from about 15 cm to about 21 cm in length.

16. The package of claim 1, wherein a force required to move the closure from the closed configuration to the open configuration is from about 3 N to about 30 N.

17. A method for accessing the at least one medical device by opening the package of claim 1, the method comprising: simultaneously pressing against the first end of the closure and the second end of the closure, thereby causing the closure to move from the closed configuration toward the open configuration; and with the closure in the open configuration, removing the at least one medical device from an interior of the flexible body through the opened at least one slit.

18. The method of claim 17, comprising pressing against the first end of the closure with an index finger of a hand and pressing against the second end of the closure with a thumb of the same hand.

19. The package of claim 1, wherein the closure comprises a through-hole extending through the closure comprising longitudinal sides and transverse sides, and wherein a first segment of the at least one slit extends from a transverse side of the through-hole toward the first end of the closure and a second segment of the at least one slit extends from an opposing transverse side of the through-hole toward the second end of the closure.

20. The package of claim 19, wherein the longitudinal sides of the through-hole are angled outwardly relative to a longitudinal axis of the closure, such that, for each longitudinal side, a shortest distance between an intermediate point of the longitudinal side and the longitudinal axis of the closure is greater than a shortest distance between ends of the longitudinal sides and the longitudinal axis of the closure.

21. The package of claim 7, wherein the transition of the closure from the closed configuration to the open configuration causes portions of the first sheet, which are not sealed to the second sheet, to move away from the second sheet.

22. The package of claim 10, wherein the first living hinge and the second living hinge are biased so that the closure remains in the open configuration after the biaxial force applied to the first end and the second end of the closure is removed.

23. The package of claim 12, wherein angles defined by the first buckling portion and the second buckling portion becomes smaller as the closure moves from the closed configuration to the open configuration.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0036] FIG. 1A is a perspective view of a package for a medical device including a pinch-open closure in a closed configuration, according to an aspect of the present disclosure.

[0037] FIG. 1B is a perspective view of the package of FIG. 1A including the pinch-open closure in an open configuration, according to an aspect of the present disclosure.

[0038] FIG. 2A is a perspective view of the pinch-open closure of FIG. 1A.

[0039] FIG. 2B is a top view of the pinch-open closure of FIG. 1A in the closed configuration.

[0040] FIG. 2C is a top view of the pinch-open closure of FIG. 1A in the open configuration.

[0041] FIG. 3A is a perspective view of another example of a pinch-open closure, according to an aspect of the present disclosure.

[0042] FIG. 3B is another perspective view of the pinch-open closure of FIG. 3A.

[0043] FIG. 4A is a schematic drawing showing a practitioner's hand in proximity to a package for a medical device, according to an aspect of the present disclosure.

[0044] FIG. 4B is a schematic drawing showing the practitioner's hand in proximity to a pinch-open closure, according to an aspect of the present disclosure.

DESCRIPTION OF THE INVENTION

[0045] The following description is provided to enable those skilled in the art to make and use the described embodiments contemplated for carrying out the invention. Various modifications, equivalents, variations, and alternatives, however, will remain readily apparent to those skilled in the art. Any and all such modifications, variations, equivalents, and alternatives are intended to fall within the spirit and scope of the present invention.

[0046] For purposes of the description hereinafter, the terms upper, lower, right, left, vertical, horizontal, top, bottom, lateral, longitudinal, and derivatives thereof shall relate to the invention as it is oriented in the drawing figures. However, it is to be understood that the invention may assume alternative variations and step sequences, except where expressly specified to the contrary. It is also to be understood that the specific devices and processes illustrated in the attached drawings, and described in the following specification, are simply exemplary embodiments of the invention. Hence, specific dimensions and other physical characteristics related to the embodiments disclosed herein are not to be considered as limiting.

[0047] With reference to the figures, the present disclosure is directed to medical device packaging, such as packages 10, bags, pouches, enclosures, and similar containers that provide a sterile barrier for tools (e.g., medical devices) used for performing medical procedures, such as fluid delivery procedures, blood draw and fluid collection procedures, and/or vascular access procedures. Medical devices that can be enclosed within the packages 10 or containers of the present disclosure can include, without limitation, surgical tools, syringes (e.g., prefilled and/or disposable syringes), catheters, vascular access devices, intravenous ports, and other disposable or single-use medical devices used for commonly performed medical procedures, as are known in the art.

[0048] As will be appreciated by those skilled in the art, the packages 10 of the present disclosure can provide a single easily transportable item that can be quickly obtained from a storage area and carried to a patient's bedside to perform a medical procedure. Further, the packages 10 of the present disclosure can reduce a risk of infection, improve quality of collected samples, and increase efficiency of medical procedures by ensuring that tools needed for performing a medical procedure are maintained in a sterile condition until ready for use.

[0049] The packages 10 of the present disclosure are designed to be easy for practitioners, such as medical technicians, nurses, physician assistants, physicians, or other trained, or untrained clinicians or medical caregivers, to manipulate and open avoiding unnecessary delays in accessing medical devices contained in the packages 10. In some particularly advantageous examples, the packages 10 of the present disclosure can be opened by the practitioner with one hand. Further, the packages 10 can be opened by touching only a small area of an external surface of the package 10, making it less likely that the practitioner will touch or contaminate other interior or exterior areas or surfaces of the package 10 or of the medical device(s) contained therein. Specifically, the practitioner desirably should be able to open the package 10 with one hand by manipulating only a first or top end of the package 10 proximate to an opening of the package 10. By contrast, for conventional pouches or bags, as previously described, the practitioner may need to grasp the package with two hands and/or may need to contact a larger area of an outer surface of the package to open to package and to remove the medical device from the package.

[0050] In some examples, the packages 10 disclosed herein are configured to be manufactured using existing production lines and without affecting production time for the existing production lines. For example, the packages 10 of the present disclosure can be manufactured by applying an additional closure, strip, or seal to existing packages, which can be accomplished by adding a single assembly step performed with the existing production lines. Accordingly, the packages 10 can be convenient to manufacture, thereby obtaining the benefits of improved sealing, reduced risk of contamination, and single-handed operation, without significantly impacting existing production processes.

Medical Device Packaging

[0051] With reference to FIGS. 1A and 1B, a package 10, such as a pouch, bag, or similar container, configured to contain a medical device (not shown), such as a vascular access device or syringe (e.g., a disposable and/or prefilled syringe), comprises a flexible pouch, bag, or body 12 configured to transition between a collapsed configuration (shown in FIG. 1A) and an expanded configuration (shown in FIG. 1B). For example, the body 12 can be a pouch or bag formed from a flexible synthetic or natural fabric, film, or sheet, such as a plastic sheet (e.g., a sheet comprising polyethylene terephthalate, polypropylene, low-density polyethylene, or combinations thereof), paper, cloth, or similar materials. As shown in FIG. 1A, in the collapsed configuration, the body 12 can be substantially flat. The body 12 expands to the expanded configuration (shown in FIG. 1B), in which the body 12 conforms to a three-dimensional shape sized to receive the medical device.

[0052] In some examples, the body 12 includes a first or open end 14, a second or closed end 16, and sides 18 extending between the open end 14 and the closed end 16. As described in further detail herein, dimensions of the body 12 are selected so that the body 12 can be easily manipulated by the practitioner with one hand. In some non-limiting examples, in the collapsed configuration (shown in FIG. 1A), the body 12 can have a height H1 of about 8.0 cm to about 21.0 cm, a length L1 of about 12.0 cm to about 15.0 cm, and a width W1 of about 0.35 cm to about 1.0 cm. In the expanded configuration (shown in FIG. 1B), the height H2 remains about the same, while the length L2 decreases, and the width W2 increases. For example, in the expanded configuration (shown in FIG. 1B), the body 12 can have a height H2 of about 8.0 cm to about 21.0 cm, a length L2 of about 10.0 cm to about 13.0 cm, and a width W2 of about 2.35 cm to about 3.0 cm.

[0053] The bag or body 12 of the present disclosure can comprise a variety of different types of pouch or flow-wrap designs made through conventional manufacturing processes. In some examples, portions of the pouch and/or flow-wrap can be the polymeric materials, such as polymeric materials that are laminated or mono-layered with internal sealing through application of heat. A sealant for the pouch and/or flow-wrap can be a scalable polymer material, such as low density polyethylene (LDPE) or an ethylene-vinyl acetate (EVA) additive structures.

[0054] In some examples, the body 12 can be formed from a first or top sheet 20 and a second or bottom sheet 22 of a flexible polymer material (e.g., polyethylene terephthalate, polypropylene, or low-density polyethylene) sealed together about portions of a periphery of the top sheet 20 and the bottom sheet 22 to form the open end 14, the closed end 16, and closed or sealed sides 18 of the body 12. For examples, the sheets 20, 22 can be adhered together by heat sealing, or with an adhesive applied near the periphery of the sheets 20, 22, to form a seal or seam between the sheets 20, 22. In some examples, the sheets 20, 22 can be coated with a protective material, such as layers of a vinyl acetate material deposited over exterior surfaces of the top sheet 20 and/or the bottom sheet 22 of the body 12. Other types of polymer materials can also be applied to the package 10 for aesthetic purposes and/or to protect the medical devices contained in the package 10. In some examples, labels, and other identifying indicia, can also be applied to or printed on surface(s) of the sheets 20, 22 to identify the medical device(s) contained in the package 10. Desirably, any coating layers or materials on the sheets 20, 22 does not prevent labels and other adhesives from being adhered to the sheets 20, 22.

[0055] With reference to FIGS. 1A and 1B, as well as FIGS. 2A-2C, the package 10 further comprises a pinch-open closure 24, such as an elongated member or plastic strip, connected to the body 12. The closure 24 can comprise a first end 26, a second end 28, and a slit 30 extending at least partially between the first end 26 and the second end 28 of the closure 24. The closure 24 can be formed from a rigid thermoplastic material, such as a homopolymer comprising polypropylene or high density polyethylene.

[0056] The closure 24 is configured to transition between a closed configuration (shown in FIGS. 1A, 2A, and 2B) and an open configuration (shown in FIGS. 1B and 2C). In some examples, an outer periphery of the closure 24, in the closed configuration, is elliptical in shape, as shown in FIGS. 1A, 2A, and 2B. In other examples, as shown in FIGS. 3A-4B, the periphery of the closure 24, in the closed configuration, can be rectangular. In the closed configuration, the closure 24 retains the pouch, bag, or body 12 of the package 10 in the collapsed configuration, scaling the open end 14 of the body 12. Specifically, the slit 30 of the closure 24 can be sealed (e.g., sealed by the heat sealing process), providing a barrier that prevents contamination of the medical devices(s) contained in the package 10. Upon application of a biaxial force to the first end 26 and the second end 28 of the closure 24, the closure 24 moves toward an open configuration. Movement of the closure 24 to the open configuration causes the body 12 of the package 10 to transition to the expanded configuration. When the closure 24 is open and the body 12 is in the expanded configuration, an interior of the pouch, bag, or body 12 is accessible through the slit 30 of the closure 24, which expands to conform to a shape of the open end 14 of the body 12.

[0057] The closure 24 can be configured to support the open end 14 of the body 12 in a variety of shapes and configurations. For example, as shown in FIGS. 1B and 2C, the open closure 24 is a parallelogram having legs that intersect forming angles that are not 90 degrees. In some examples, all four legs of the parallelogram can be the same length, as shown in FIG. 2C. In other examples, the parallelogram can include two short legs and two longer legs, as shown in FIG. 1B. In other examples, the closure 24 can be configured to maintain a variety of other shapes, including a square, rectangle, diamond, an irregular polygon shape, ellipse, oval, or circle, within the scope of the present disclosure.

[0058] As used herein, the biaxial force applied to the closure 24 refers to axial forces that are simultaneously applied to an elongated member in opposite directions. For example, inwardly directed axial forces can be applied to the ends 26, 28 of the closure 24, as shown by arrows A1 in FIGS. 2B and 2C, in order to cause the closure 24 to transition from the closed configuration to the open configuration.

[0059] As shown in FIGS. 1A and 1B, the closure 24 is connected to the body 12 proximate to the open end 14 of the body 12. In some examples, the closure 24 can be embedded in the body 12. For example, layers or sheets of plastic material can be laminated over or around surfaces of the closure 24, thereby securing the closure 24 to the body 12.

[0060] In other examples, the closure 24 can be connected to the body 12 using a conventional adhesive, as is known in the art. For example, a peripheral surface of the closure 24 can be adhered to inner surfaces of sheets 20, 22 of the body 12 by applying a small amount of the adhesive to the surfaces of the closure 24 and body 12 and then curing or drying the adhesive to seal the closure 24 to the body 12. In other examples, the sheets 20, 22 that form the body 12 can be inserted through the slit 30 of the closure 24, such that the outer surfaces of the sheets 20, 22 are adhered to the inner surface of the slit 30.

[0061] In some examples, the fixture or closure 24 can be attached to an inside of body 12 during formation of the package 10 and prior to sealing portions of the sheets 20, 22 together creating a scaled package 10. In particular, the fixture or closure 24 can be fixed within the body 12 below the sealed portion of the body 12. The closure 24 can be held in place by applying heat to the body 12 while polymeric films of the body 12 are laminated around the closure 24. Alternatively or in addition, the adhesive can be applied between the closure 24 and the body 12, as the body 12 is being laminated, to adhere the closure 24 to the body 12. The sheets 20, 22 of the body 12 are then scaled at a position above the closure 24 to form the sealed package 10.

[0062] In some examples, portions of the closure 24 can be biased to the open configuration, meaning that, once partially opened, the closure 24 can automatically move to a fully opened configuration (as shown in FIG. 2C) without requiring the practitioner to continue to apply the biaxial force to the closure 24. Further, in some examples, the closure 24 can be configured to remain in the fully opened configuration even after application of the biaxial force to the closure 24 ceases.

[0063] As shown in FIGS. 2A-2C, in some examples, the closure 24 comprises living hinges 32, 34 at the ends 26, 28 of the closure 24 with axially-extending segments or parts 36, 38 extending between the living hinges 32, 34 and separated by the slit 30. As used herein, a living hinge refers to a hinge formed from a thin flexible segment or portion of an object made of a same material as two more rigid portions or segments of the object connected by the thin flexible living hinge. The living hinge is capable of bending to open and close in a similar manner to hinges formed between separate rigid pieces connected to a post, pin, or rotation point. For example, as shown in FIGS. 2A-2C, the closure 24 includes the living hinges 32, 34 extending between the rigid axially-extending segments or parts 36, 38 of the closure 24.

[0064] In some examples, the closure 24 also includes notches, grooves, recesses, or gaps, which form weakened buckling portions 40, 42 of the segments or parts 36, 38, positioned between the living hinges 32, 34. The weakened buckling portions 40, 42 are portions of the closure 24 that bend or deform as the closure 24 moves between the closed configuration (in FIGS. 2A and 2B) and the open configuration (in FIG. 2C). In particular, the buckling portions 40, 42 can be narrow flexible segments between wider, more rigid, segments of the parts 36, 38. The buckling portions 40, 42 can form angles (shown by angles ?1 and ?2 in FIGS. 2B and 2C) that close (e.g., become smaller) as the closure 24 moves from the closed configuration to the open configuration. For example, as shown in FIG. 2B, the angles ?1, ?2 in the open configuration can be nearly 180 degrees. As the closure 24 moves to the open configuration, the angles ?1, ?2 can approach, for example, 120 degrees, 100 degrees, or 90 degrees, as shown in FIG. 2C.

[0065] The buckling portions 40, 42 can be formed from a bulbous or widened area 44 of the slit 30 positioned such that a width W3 (shown in FIGS. 2A and 2B) of the buckling portions 40, 42 is less than a width W4 (shown in FIGS. 2A and 2B) of other portions of the segments or part 36, 38. For example, the width W3 of the buckling portions 40, 42 can be about 0.3 mm to about 0.7 mm. The width W4 of other portions of the segments or parts 36, 38 can be about 3.0 mm to about 5.0 mm.

[0066] Positioning of the buckling portions 40, 42 on the parts 36, 38 affects the shape of the closure 24 in the open configuration. For example, as shown in FIGS. 2A-2C, the closure 24 can include a buckling portion 40, 42 on each of the segments or parts 36, 38 of the closure 24. The buckling portions 40, 42 can be equidistantly spaced or substantially equidistantly spaced between the ends 26, 28 of the closure 24, such that in the open configuration, the closure 24 forms a square or parallelogram with substantially equal length legs, as shown in FIG. 2C. Alternatively, the buckling portions 40, 42 can be positioned closer to one of the ends 26, 28 of the closure 24 than the other end, such that, when expanded, the closure 24 forms a rectangle or parallelogram with two short legs and two long legs, as shown in FIG. 1B.

[0067] In some examples, the closure 24 can be made by conventional molding methods, as are known in the art. For example, the closure 24 can be an integral part comprising the living hinges 32, 34 and segments or parts 36, 38 formed together by a same material in a single injection molding process.

[0068] In some examples, dimensions and mechanical features of the closure 24 are selected so that the package 10 can be easily and comfortably opened by an average-sized adult individual applying a reasonable pinching force to the ends 26, 28 of the closure 24 with one hand. In particular, a length L3 (shown in FIG. 2B) of the closure 24, in the closed configuration, can be selected based on an average distance between index finger and thumb for an adult, which has been found to be about 18 cm. For example, the length L3 of the closure 24, in the closed configuration, can be about 15 cm to about 21 cm. In other examples, the length L3 of the closure 24 can be less than 18 cm or, preferably less that about 15 cm to accommodate practitioners with slightly smaller than average hand size. Similarly, the force required to move the closure 24 from the closed configuration to the open configuration can be selected taking into account a maximum pinching force that an average adult can comfortably provide between a finger and thumb, which has been found to be about 60 N for men and about 45 N for women. Therefore, the maximum force required to cause the closure 24 to open can be less than or substantially less than 45 N. For example, the closure 24 can be configured to open when a force of about 3.3 N to about 17 N, or preferably about 3 N to about 12 N, is applied to the ends 26, 28 of the closure 24 to accommodate practitioners with less than average pinch and/or grip strength.

[0069] FIGS. 3A and 3B show another example of a closure 24 that can be used with the package 10 of the present disclosure. For example, the closure 24 of FIGS. 3A and 3B can be used for gusseted bags. By contrast, in previous examples of FIGS. 2A-2C, the bag or body 12 of the package 10 is a pouch. The closure 24 of FIGS. 3A and 3B is similar to previous examples and, in particular, includes an elongated member having a first end 26, a second end 28, and the axially-extending segments or parts 36, 38 extending between the first end 26 and the second end 28. The closure 24 also includes the slit 30 which forms a gap or space between the segments or parts 36, 38 of the closure 24. The closure 24 also includes the living hinges 32, 34.

[0070] As in previous examples, the closure 24 is configured to transition between a closed configuration and an open configuration. In the closed configuration, the closure 24 retains a bag, pouch, or body 12 of the package 10 in a collapsed configuration. Upon application of a biaxial force to the first end 26 and the second end 28 of the closure 24, the closure 24 transitions to the open configuration. As previously described, causing the closure 24 to move from the closed configuration to the open configuration causes the body 12 of the package 10 to transition to the expanded configuration.

[0071] Unlike in previous examples, the closure 24, shown in FIGS. 3A and 3B, has a rectangular shaped periphery in the closed configuration. Further, the segments or parts 36, 38 of the closure 24 are substantially straight. By contrast, in previous examples (shown in FIGS. 1A-2C), the periphery of the closure 24 is elliptical and the outer edges of the segments or parts 36, 38 are curved. In some cases, a rectangular shaped closure 24 may be easier to mold and manufacture than closures 24 having a complex curvature. Accordingly, the closure 24 of FIGS. 3A and 3B may be preferred to simplify manufacturing.

Method of Opening a Medical Package

[0072] As previously described, the packages 10 of the present disclosure will generally be provided pre-filled with one or more medical devices intended for use for a medical procedure. For example, the packages 10 can contain one or more syringes (e.g., a disposable and/or prefilled syringe) or another type of vascular access device. As previously described, the exemplary packages 10 and closures 24 disclosed herein are intended to be easy to manipulate and open so that practitioners can obtain medical devices and tools contained in the packages 10 without disrupting other aspects of a medical procedure being performed for a patient. For example, the packages 10 can be opened with one hand and, in some cases, without looking at the package 10 and closure 24 so that the practitioner can continue to perform other tasks and/or can continue to visually monitor the patient while opening the package 10.

[0073] FIGS. 4A and 4B are schematic drawings showing the package 10 being grasped by a practitioner to open the package 10. A method for opening the package 10 can include the following steps. Initially, when ready for use, the practitioner grasps the package 10 in one hand 50 and simultaneously presses against the first end 26 of the closure 24 and the second end 28 of the closure 24, as shown by arrows A1 in FIGS. 4A and 4B. For example, the practitioner can grasp the package 10 between the thumb 52 and index finger 54, with the thumb 52 positioned proximate to the first end 26 of the closure 24, and the index finger 54 positioned proximate to the second end 28 of the closure 24.

[0074] The practitioner then performs a pinching motion moving the index finger 54 and the thumb 52 towards one another to apply the biaxial force to the opposing ends 26, 28 of the closure 24. An initial amount of biaxial force may be sufficient to overcome or release a seal between the segments or parts 36, 38 of the closure 24. Once the seal releases, the practitioner continues to apply the biaxial force to the closure 24, which causes the segments or parts 36, 38 of the closure 24 to move away from each other, as shown by arrow A2 in FIGS. 4A and 4B. The biaxial force applied to the closure 24 ultimately causes the closure 24 to move from the closed configuration toward the open configuration.

[0075] As previously described, as the closure 24 moves to the open configuration, the buckling portions 40, 42 of the closure 24 bend or deform causing the closure 24 to adopt a shape of a square, rectangle, or parallelogram. Also, moving the closure 24 to the open configuration causes the bag or body 12 of the package 10 to move to the expanded configuration. Once the closure 24 is in the open configuration and the body 12 is expanded, the practitioner can remove the medical device from the package 10 through the open end 14 of the body 12 and through the open closure 24.

[0076] Once the desired item is removed from the package 10, the practitioner can close the package 10. If the closure 24 is biased to the closed configuration, the practitioner can simply release the closure 24, allowing the closure 24 to automatically return to the closed configuration. Alternatively, if the closure 24 is not biased to the closed configuration, the practitioner can either pull the ends 26, 28 of the closure 24 away from each other or apply a biaxial force to the buckling portions 40, 42 of the closure 24, thereby causing the closure 24 to return to the closed configuration. As the closure 24 moves to the closed configuration, the bag or body 12 of the package 10 returns to a more contracted or compressed configuration as shown, for example, in FIG. 1A.

[0077] While examples of the packages 10, containers, and methods are shown in the accompanying figures and described hereinabove in detail, other examples will be apparent to, and readily made by, those skilled in the art without departing from the scope and spirit of the invention. Accordingly, the foregoing description is intended to be illustrative rather than restrictive. The invention described hereinabove is defined by the appended claims and all changes to the invention that fall within the meaning and the range of equivalency of the claims are to be embraced within their scope.