HYBRID SAFETY SPRING CLIP FOR SHARP MEDICAL DEVICES AND RELATED METHODS
20220280756 · 2022-09-08
Assignee
Inventors
Cpc classification
A61M25/0618
HUMAN NECESSITIES
A61M25/0625
HUMAN NECESSITIES
International classification
Abstract
Needle guards that can be made from a combination of plastic and metal can be used with sharp medical devices. The needle guard can have a proximal wall defining a distal surface, a proximal surface, and a through opening, the proximal wall being made of a first material. The needle guard can have a first resilient arm extending distally from the distal surface of the proximal wall, the first resilient arm comprising an arm section and a distal wall. The needle guard can have a second resilient arm extending distally from the distal surface of the proximal wall, the second resilient arm comprising an arm section and a distal wall. One of the first resilient arm and the second resilient arm can be made of a second material different from the first material of the proximal wall.
Claims
1-15. (canceled)
16. A needle guard comprising: a proximal wall having a distally facing surface, a proximally facing surface, and a perimeter defining a through opening, the proximal wall being made of a first material; a first arm extending distally from the distally facing surface of the proximal wall, the first arm comprising an arm section and a distal wall; a second arm extending distally from the distally facing surface of the proximal wall, the second arm comprising an arm section and a distal wall; wherein the first arm, the second arm, or both the first arm and the second arm are made of a second material different from the first material of the proximal wall.
17. The needle guard according to claim 16, wherein the first arm and the second arm are made of the same second material.
18. The needle guard according to claim 16, further comprising an adaptor attached to the proximal wall.
19. The needle guard according to claim 18, wherein the adaptor comprises at least one engagement tab, the engagement tab comprising a locating protrusion for contacting a catheter hub.
20. The needle guard according to claim 19, wherein the engagement tab extends from a side surface of an adaptor body of the adapter and comprises a bend such that the engagement tab extends in a proximal direction or a distal direction.
21. The needle guard according to claim 19, wherein the engagement tab comprises a locating projection projecting from a surface of the engagement tab.
22. The needle guard according to claim 18, wherein the adaptor comprises two or more engagement tabs.
23. The needle guard according to claim 22, wherein at least two of the two or more engagement tabs are diametrically opposed around an adaptor body.
24. A needle guard for a sharp medical device, the needle guard comprising: a proximal wall having a distally facing surface, a proximally facing surface, a side surface, and a perimeter defining a through opening; a first arm and a second arm extending distally of the proximal wall; and (1) an adaptor located between the first arm and the second arm and attached to the proximal wall, the adaptor having a first engagement tab and a second engagement tab extending from an adaptor body, each of the first engagement tab and the second engagement tab comprising a locating protrusion for contacting an interior surface of a hub or a housing; or (2) a wall guard having a surface covering a portion of the first arm.
25. The needle guard according to claim 24, wherein the first engagement tab extends from a side surface of the adapter body and comprises a bend such that the first engagement tab extends in a proximal or a distal direction from the bend.
26. The needle guard according to claim 24, wherein the first arm comprises a tooth to engage with the wall guard.
27. The needle guard according to claim 24, further comprising an insert having a bore aligned with the through opening of the proximal wall.
28. A method of manufacturing a needle guard comprising: stamping a material sheet to form a central portion, a first pair of opposed strips of material extending from the central portion, and a second pair of opposed strips, the central portion comprising an opening; covering a portion of at least one strip of material with a plastic guard; bending each of the first pair of opposed strips at a first location to form a first arm and a second arm and bending each of the first pair of opposed strips at a second location to form a distal wall on the first arm and a distal wall on the second arm; bending each of the second pair of opposed strips at a first location to form a first engagement tab and a second engagement tab; wherein the first arm, the second arm, the first engagement tab and the second engagement tab are spaced around the central portion.
29. The method of manufacturing of claim 28, further comprising placing the distal wall of the first arm into a slit of a wall guard.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0130] These and other features and advantages of the present devices, systems, and methods will become appreciated as the same becomes better understood with reference to the specification, claims and appended drawings wherein:
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DETAILED DESCRIPTION
[0159] The detailed description set forth below in connection with the appended drawings is intended as a description of the presently preferred embodiments of needle guards for IV catheters and other sharp medical devices provided in accordance with aspects of the present devices, systems, and methods and is not intended to represent the only forms in which the present devices, systems, and methods may be constructed or utilized. The description sets forth the features and the steps for constructing and using the embodiments of the present devices, systems, and methods in connection with the illustrated embodiments. It is to be understood, however, that the same or equivalent functions and structures may be accomplished by different embodiments that are also intended to be encompassed within the spirit and scope of the present disclosure. As denoted elsewhere herein, like element numbers are intended to indicate like or similar elements or features.
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[0161] The proximal wall 280 may have an opening 284 defined by a perimeter. The opening 284 can be sized and shaped to allow a needle or cannula to pass through the proximal wall 280. If the needle incorporates a crimp, a sleeve, or a material buildup, which can generally be referred to as a change in profile, the diameter of the opening 284 can be smaller than the change in profile so that there is an interference between the opening, or the perimeter of the opening, and the change in profile.
[0162] As understood in embodiments of IV catheter assemblies, such as shown in PCT/EP2016/069619, published as WO/2017/029361, the contents of which are expressly incorporated herein by reference, the needle, which is attached to a needle hub, can be inserted through the opening 284 of the proximal wall 280 such that it can protrude from a distal opening of a catheter tube when the needle guard 132 is assembled in an IV catheter assembly in a ready to use position. An exemplary embodiment and description of a catheter assembly is shown below with respect to
[0163] At least one guard arm 288 extends distally of the proximal wall 280. As shown in
[0164] In an embodiment, the needle guard 132 can be formed from a plastic material. For example, the needle guard can be formed by plastic injection molding. The two arms 288, 290 can be molded so that they are hinged from the proximal wall 280 and are normally curved or pointed in the direction of the lengthwise axis X so that when the arms are spread outwardly away from one another, such as when the needle guard is mounted onto a needle, the two arms bias inwardly towards one another, such as having a restoring force to move towards one another. In other examples, metal inserts can be co-molded or insert molded with the two arms to increase the restoring force of the two arms. In still other examples, adapters or attachments can be incorporated with the two arms to increase their restoring force, as further discussed below.
[0165] In some embodiments, the first arm section 292 and the second arm section 294 can have a stadium shape cross sectional shape, which can be understood as a geometric shape constructed of a rectangle with semicircles at a pair of opposite corners. However, the cross-sectional shape can embody other geometries, such as rectangular, oval, elliptical, polygonal, irregular, etc. In some embodiments, the first arm section 292 and the second arm section 294 can have a substantially uniform thickness and the first width of the first arm section 292 can transition to the second width of the second arm section 294 with an increasing width tapering section 293. As such, in embodiments, each of the two arms 288, 290, which can be resilient, can be understood as having a narrow first arm section 292 extending distally from the proximal wall 280. The arms 288, 290 can then increase in width in the tapering section 293 as they extend distally from the proximal wall 280. The second arm section 294 can thereby be a distal portion of the arms 288, 290 that is wider than the first arm section 292. As used herein, the arms being resilient is understood to mean being able to spring back into shape. For example, when the two arms are spread apart by the needle, the resilient arms can spring back after retraction of the needle proximally of the one or more distal walls of the needle guard so that the arms can block the needle tip. As further discussed below, such as with reference to
[0166] The two arms 288, 290 can be circumferentially spaced around the opening 284 on the proximal wall. In some embodiments, the two arms 288, 290, which can be resilient, can be spaced 180 degrees from each other circumferentially around the opening 284. In other embodiments, the two arms 288, 290 can be spaced apart at different positions circumferentially from 180 degrees.
[0167] Two distal walls 300, 302 can be provided with the needle guard 132, one at an end of each of the two resilient arms 288, 290. Each of the distal walls 300, 302 can extend at an angle from the respective second arm section 294 of the two resilient arms 288, 290. The distal walls 300, 302 may extend towards each other. The two distal walls can have surfaces with lengths and widths that are sufficient to cover or block a needle tip. The surfaces can be located at or on two different side sections of the needle in a ready to use position and movable distal of the needle in a protective position to block the needle tip from inadvertent needle sticks. The lengths, which can be considered the direction extending from the respective second sections toward the axis X, can be selected so that the two distal walls overlap in a protective position. Alternatively, only one distal wall is incorporated, on one of the two arms, and the other arm can have a free end without a distal wall. Another alternative is a needle guard with only one arm with one distal wall at an end of the one arm.
[0168] The distal walls 300, 302 preferably overlap one another along the axis X of the needle guard 132 by utilizing different arm lengths of the two resilient arms 288, 290 and/or angling at least one of the distal walls 300, 302 at an elbow or diagonal section 304 between the distal wall and the resilient arm. As shown in
[0169] Alternatively, the two arms can be equal in length such that the distal walls 300, 302 abut one another or the distal walls can be angled from the second arm sections at different angles as they project toward the axis to allow for overlapping.
[0170] In fitment with an IV catheter hub of a catheter assembly, the arms 288, 290 are sufficiently flexible to allow for deflection radially outward such that the needle can extend through the opening 284 and extend distally between the two distal walls 300, 302 of the two arms 288, 290 when the IV catheter assembly is in the ready to use position. In the ready to use position, where the arms 288, 290 are deflected radially outward by the presence of the needle between the two distal walls, the arms 288, 290 preferably have a restoring force acting on the needle. Upon withdrawal of the needle after successful venipuncture, when the needle is moved proximal of the two distal walls 300, 302, the arms 288, 290, which can be resilient and have restoring forces, move back towards the axis X of the needle guard 132. In this way, the distal walls 300, 302 shield the needle from accidental finger pricks after withdrawal of the needle. The overlapping configuration of the two distal walls 300, 302 can restrict the needle tip from projecting between the two distal walls to re-emerge from the needle tip holding space proximal of the two distal walls.
[0171] In some embodiments, the two arms 288, 290 can each extend substantially parallel to one another. The two arms 288, 290 can each extend perpendicularly from the distally facing wall surface 287 of the proximal wall 280. The two arms can be singularly formed with the proximal wall and hinged off of the proximal wall.
[0172] In other embodiments, the two arms 288, 290 can each extend at an oblique angle relative to the distally facing wall surface 287 of the proximal wall 280. In embodiments, the two arms 288, 290 can each extend from the distally facing wall surface 287 at an angle ranging from 20 degrees to 89 degrees. More specifically, the two arms 288, 290 can each extend from the distally facing wall surface 287 at an angle ranging from 45 degrees to 80 degrees. The two arms 288, 290 may be angled such that they extend towards each other.
[0173] Although the embodiment shown in
[0174] In other embodiments, more than two guard arms may be used. For example, three or four or more guard arms may be incorporated with a needle guard of the present disclosure. The resilient arms may be equally spaced around the opening 284 at the distally facing wall surface of the proximal wall. Each of the guard arms can be arranged such that distal walls of the guard arms can overlap one another along the axial direction of the needle guard.
[0175] Embodiments of the needle guard 132 may have a proximal wall 280 and the guard arms 288, 290 made of different materials.
[0176] In some embodiments, the needle guard 132 may be made from plastic and metal materials. By using both plastic material and metal material, the needle guard 132 may be made in a more economical way by reducing the amount of metal needed.
[0177] For example, some embodiments of the proximal wall 280 may be made from a plastic material and the arms 288, 290 may be made from a metal material or be provided with both plastic and metal components, such as forming the arms as a hybrid. Using a metal material may can increase the biasing forces of the arms and increase shelf life as the metal will not set like some plastics might. In the case of some plastics, the plastic may set while being biased in the ready to use position due to a phenomenon called plastic creep. Creep is the tendency of a solid material to move slowly or deform permanently under the influence of mechanical stresses. Thus, including a metal component to the plastic component can maintain the resiliency of the overall hybrid structure even after prolonged storage or after periods of un-used.
[0178] Embodiments with the proximal wall 280 made from a plastic material and the arms 288, 290 made at least in part from a metal material may be formed by insert molding. For example, the proximal wall 280 may be insert molded around an end of the resilient arms 288, 280.
[0179] Alternatively, in some embodiments, the proximal wall 280 and the resilient arms 288, 290 may be manufactured separately. The proximal wall 280 may have slots 289 (
[0180] In some embodiments, one of the guard arms may be made from a metal material and another one of the guard arms may be made from a plastic material. In an example, the proximal wall 280 can be made out of metal and have slots 289, and the arms 288, 290 made from a plastic material and be inserted into the slots 289 in the proximal wall. In embodiments, the proximal end of the plastic arms 288, 290 could include at least one hook feature or projection in order to snap into the slots on the proximal wall and hook themselves fixedly to the proximal wall 280.
[0181] In other embodiments, the needle guard 132 may be formed from plastic materials by methods such as plastic injection. Embodiments of the needle guard formed from plastic material may have the proximal wall 280 and the arms 288, 290 unitarily formed. Alternatively, the proximal wall 280 and the arms 288, 290 may be separately formed and then attached together by plastic welding or adhesives. The arms can be provided with ribs or increased bulk mass extending at least partly along the length of each arm to increase the arm's restoring force.
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[0184] In some embodiments, the adaptor body 351 can be generally cylindrical along an end view. The adaptor body 351 can correspond in shape and size to match the proximal wall 280. That is, the side surface 356 of the adaptor 350 can have a same diameter as the side surface 285 of the proximal wall 280 of the needle guard 132. In other embodiments, only parts or sections of the body 351 of the adaptor can have points that are coincident with the side surface 285 of the proximal wall. For example, a square adaptor body 352 can have four points that lie on the same outer surface profile as the side surface 285 of the proximal wall 280. At least one engagement tab 358 can extend from adaptor body 351. In an example, the at least one engagement tab 358 can extend from the side surface 356 of the adaptor 350. In the embodiment shown in
[0185] The engagement tabs 358 may join to the side surface 285 at an angle through a bend or elbow section 360. That is, the engagement tabs 358 can extend in the proximal direction due to the bend 360. In some embodiments, the bend 360 may be a 90-degree bend. As such, the engagement tabs 358 can be located at a position radially outward from the adaptor body 351. In some examples, the engagement tabs 358 are stamped from the same metal blank as the adaptor body 351 and then the bends or elbows 360 are simply formed as by-products in cold-working the tabs to point in the proximal direction.
[0186] Each of the engagement tabs 358 may have at least one locating protrusion or projection 362. The locating projection 362 can project from a surface of the engagement tab 358. In an example, the locating projection 362 projects from the side or surface of the engagement tab that faces the interior of a hub housing, such as a catheter hub or a third hub. The at least one locating protrusion 362 can be oriented to contact a surface, such as the interior surface of a catheter hub. Thus, the engagement tab can face radially outward away from the axis X of the needle guard. The locating protrusion 362 may be a hemispherical protrusion or a portion of a sphere on the engagement tab. Alternatively, other geometric shapes could be used, such as a rectangular rib, a trapezoidal or half or partial oval shape. Preferably locating protrusion is smooth to avoid scratching the inside of the catheter hub. The locating protrusion 362 can be arranged to contact an interior of a catheter hub as described in
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[0190] The adaptor 350 can be formed from metal. In some embodiments, the adaptor 350 can be formed by stamping and bending a metal sheet to form the engagement tabs 358 and the locating detents 362. In some embodiments where the proximal wall 280 of the needle guard is made of plastic, the proximal wall 280 can be co-molded or insert molded with the adaptor 350. Furthermore, in such cases, the stamping and bending of the metal sheet can provide for bonding tabs extending distally from the distal surface 352. These bonding tabs can facilitate bonding with the plastic of the proximal wall 280 by either providing a contact surface for insert molding or to provide a feature for snap fitting to the proximal wall 280.
[0191] Alternatively, in some embodiments, the proximal wall 280 can be formed with engagement tabs 358. That is, the proximal wall 280 could serve as the adaptor body 351, making it a unitary construction. As such, embodiments of this type would not require a separate adaptor 350. Instead, the proximal wall 280, such as that shown in
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[0193] In the ready position, a needle cannula 108 is inserted through the opening of the adaptor 350, the opening of the needle guard 132, the catheter hub 106, and the catheter tube 104. Due to the positioning of the needle through the openings of the adaptor and the needle guard in the ready to use position, the two arms 288, 290 are deflected radially outward by the presence of the needle. Due to this deflection, the arms 288, 290 can have a restoring force acting on the needle. In other examples, the arms can be provided or reinforced with metal strips or arms to increase the restoring forces, or providing with an elastic band to add to the restoring force. Upon withdrawal of the needle after successful venipuncture, when the needle is moved proximally of the distal walls 300, 302, the resilient arms 288, 290 are no longer biased by the needle and can move radially inwardly towards the axis X of the needle guard 132. This then allows the distal walls 300, 302 to cover the needle tip.
[0194] Due to a change in profile of the needle, such as a crimp, weld, sleeve, or material build-up, further withdrawal of the needle in the proximal direction would result in the change in profile of the needle 108 engaging the perimeter defining the opening on the proximal wall 280 or the opening 364 (
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[0196] As shown in
[0197] In the embodiment of
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[0199] As shown in
[0200] With the opposed cut outs 370 of the adaptor body 351, the adaptor body 351 has a shape that resembles the letter “H”. Said differently, the adaptor body 351 can have two generally upstanding branches that are connected to one another by a generally horizontal branch. The adaptor body 351 has a central cross member 372 defined by the opposed cut outs 370. A perimeter defining an opening 364 can be located at the central cross member 372. Each end of the central cross member 372 can be attached to an upstanding structure or frame portion 374 defining the side surface 356 of the adaptor body 350. As such, the central cross member 372, the frame portions 374, and the cut outs 370 can collectively define the cylindrical shape of the adaptor body 351.
[0201] The engagement tabs 358 can extend from the frame portions 374 and extend in the proximal direction. The engagement tabs 358 can be equally spaced around the circumference defined by the side surface 356. There can be one or more engagement tabs 358. As shown in
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[0205] In the embodiment of
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[0207] In operation with the hybrid guard 100 mounted onto a needle, withdrawal of the needle proximally relative to the hybrid guard 100 will force the adaptor 350 to move in the proximal direction due to the interaction between a change in profile of the needle engaging the perimeter defining the opening 364 of the adaptor 350 as the needle retracts in the proximal direction relative to the hybrid guard. Accordingly, upon retraction of the needle, the adaptor 350 will be moved in the proximal direction with the needle to move against the proximal wall 280 for maintaining the coupling of the needle guard 132 to the adaptor 350. In some embodiments, the diameter of the opening 364 of the adaptor 350 can be smaller than the opening 284 of the proximal wall 280 on the needle guard.
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[0210] The biasing plate 353 of the adaptor 350 is configured to bias a resilient arm of the needle guard towards the needle shaft, when in used with a needle. The adaptor 350, with the biasing plate 353, is also configured to hold the needle guard inside the catheter hub, with the aid of the engagement tabs 358. In an example, two adaptors 350 of the present embodiment can be used with a needle guard. When the resilient arms of the needle guard are biased radially outward by the presence of a needle in a ready to a use position, the biasing plate 353 on each adaptor is also biased outwardly by and has a restoring force. As such, the bias provided by the two biasing plates 353 on the two resilient arms 288, 290 of the needle guard ensure that the resilient arms 288, 290 will move to a blocking position and cover the needle tip even if the arms are plastic and have taken a set during storage.
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[0212] In some embodiments, the partial circle of the adaptor body, such as the proximally facing surface of the adaptor body, can be used for bonding or affixing with the distally facing surface of the proximal wall 280 of the needle guard. Optionally, one or both adaptors can be co-molded or insert molded with the needle guard.
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[0214] The present embodiment includes a center adaptor plate 390, configured to reinforce the opening 284 on the proximal wall 280 of the plastic needle guard 132. As shown, the center adaptor plate 390, which can be made from a metal material, is generally rectangular in shape and comprises a perimeter defining an opening 392. The opening 392 can be smaller than the largest dimension of a change in profile so that when used with a needle, proximal movement of the needle relative to the hybrid clip 100 will cause the change in profile to engage the opening 392. With further proximal movement and after the engagement, the change in profile can cause the hybrid clip 100 to then move in the proximal direction with the needle. The center adaptor plate 390 can attach to the proximal wall 280 via adhesive or bonding, or by insert or co-molding.
[0215] In an alternative embodiment, the three metal inserts of
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[0217] Alternatively,
[0218] Again, as with all of the embodiments, the engagement tabs 358 may optionally be bent so that the free ends of each engagement tab extend in the distal direction or in the proximal direction.
[0219] In some embodiments, a hybrid clip 100 of the present invention can have at least one adaptor 350 with at least two engagement tabs 358, and wherein at least one of the engagement tabs 358 extends in the proximal direction and at least one of the engagement tabs 358 extends in the distal direction. Still optionally, a hybrid clip 100 of the present invention can have two adaptors 350 with each adaptor 350 having at least one engagement tab 358, and wherein at least one of the engagement tabs 358 extends in the proximal direction and at least one engagement tab 358 extends in the distal direction.
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[0222] Each of the strips 257, 257 on the stamped material sheet 225 can be bent in at least two locations to form the resilient arms 288, 290 and the engagement tabs 270. A first bend 281 can be performed near the center portion 255 for each longer strip 257. For the resilient arms 288, 290, a second bend 283 can be performed at an intermediary location along the strip 257 of material to form a distal wall. In this way, the resilient arms can be formed with distal walls 300 and 302 (
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[0226] In terms of retention of the needle guard 132 of
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[0229] At the distal portion of the first resilient arm 288, a curved protrusion or hook 128 can be incorporated. For example, the stamped metal sheet for forming the needle guard can be cold worked to form the curved protrusion or hook 128 at an end of the resilient arm 288. The curved protrusion 128 can include a first section 130 and a second section 134. The first section 130 can extend radially outwardly away from a lengthwise axis defined by the needle guard, and then terminated with a curved section to form the second section 134. The needle guard 132 may have more than one curved protrusion of the same size or of different sizes.
[0230] The second resilient arm 290 can incorporate a distal wall 302 extending at an angle to the lengthwise section of the arm, downstream of a curved protrusion 128, which has a first section 130 and second section 128. In some embodiments, the distal wall 302 can contact the curved protrusion 128 of the first resilient arm 288. As such, when the needle guard 132 of the present embodiment is in used and after a needle is withdrawn in a proximal direction relative to the needle guard following successful venipuncture, the single distal wall 302 can move back to cover the needle tip.
[0231] As shown, the second arm 290 has a second curved protrusion 128 at an end part of the distal wall 302. The second curved protrusion 128 can be smaller in size than the curved protrusion 128 on the first arm 288 so that when the two arms move closer together in the used position to cover the needle tip from inadvertent needle sticks, the smaller second curved protrusion 128 can recess within the larger profile of the larger curved protrusion 128 on the first arm 288. In other example, the two curved protrusions have approximately the same size so that the distal wall 302 is forced to deflect slightly outwardly in the distal direction when the needle guard is in the protected position shown in
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[0233] The second distal wall guard embodiment 310 can embody a plate. In a particular example, the second distal wall guard embodiment can resemble a wedge or a wedge shape structure along a side cross-section. The distal wall guard 310 can be solid piece of plastic to be inserted on the proximal side of the distal wall 302 and held in place by fitment with the upstream and downstream curved protrusions 128 at the distal wall 302. In some embodiments, the plastic insert for the distal wall guard 310 can be taken from a roll, inserted into the clip from the side and then cut off from the rest of the roll. The distal wall guards may be held in place with contact with teeth 296.
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[0235] In some embodiments, the insert 400 may have clips 402a and 402b for clipping attachment to the needle guard 132. In an example, a stamped plate is formed with the insert 400, such as co-molded, insert molded, or bonded with the insert. The stamped plate is then folded around the proximal wall 280 to secure insert to the proximal wall. The stamped plate having the clips 402a, 402b can include a perimeter defining an opening for passing the needle therethrough. The opening on the stamped plate can have a smaller dimension than the largest dimension of the change in profile on the needle to enable the change in profile to engage the opening. The insert 400 is configured to guide the needle guard 132 and the needle during relative movement to limit or strict side-to-side or pivoting movement of the needle relative to the needle guard.
[0236] In some embodiments, the insert 400 can have a bore with a bore diameter that is slightly larger than the maximum diameter of the change in profile of the needle so that the crimp can be retracted to the metal proximal wall of the stamped plate to engage the opening. Alternatively, the bore of the plastic insert can also be smaller than the maximum diameter but slightly larger than a diameter of the needle shaft. In some embodiments of the latter case, the plastic insert can be placed on the proximal side of the proximal wall and it can be shorter as the clearance between the needle shaft and the guide bore can be kept to a minimum.
[0237] Methods of making and of using needle guards, adaptors for use with needle guards, needle assemblies and catheter assemblies for use with needle guards, including hybrid clips, of the present invention and components thereof as described herein are within the scope of the present disclosure. The methods are understood to include the use of a catheter assembly and withdrawing the needle such that surfaces of the needle guard are located to a side of the needle and then movable distal of the needle tip to cover the tip of the needle from inadvertent needle sticks.
[0238] Although limited embodiments of the needle guard, adaptor, needle assemblies and catheter assemblies and their applications have been specifically described and illustrated herein, including their components, many modifications and variations will be apparent to those skilled in the art. For example, the various features of the needle guards and the adaptors described herein may incorporate alternate materials, etc. Furthermore, it is understood and contemplated that features specifically discussed for one needle guard embodiment may be adopted for inclusion with another needle guard embodiment, provided the functions are compatible. Accordingly, it is to be understood that needle guards and their applications in catheter assemblies and needle assemblies constructed according to principles of the disclosed devices, systems, and methods may be embodied other than as specifically described herein. The disclosure is also defined in the following claims.