US20180353712A1

US20180353712A1 - Needle assembly

Info

Publication number: US20180353712A1
Application number: US16/108,437
Authority: US
Inventors: Geoff Clark
Original assignee: Smiths Medical ASD Inc
Current assignee: Smiths Medical ASD Inc
Priority date: 2011-08-31
Filing date: 2018-08-22
Publication date: 2018-12-13
Also published as: US10086151B2; US20140039414A1

Abstract

A needle assembly has a needle hub that has a body to which are formed two plates at opposite sides thereof in a parallel relationship. The plates have respective upper edges and lower edges that lie substantially along respective planes, so that the needle hub may be stably placed onto a surface by means of the respective edges. A partition is formed orthogonally proximate to the front ends of the parallel plates. The partition and the parallel plates together provide upper and lower three point stable supports for the needle hub. A notch at the partition provides a guided line of sight to the tip of the needle for the user. The connector at the proximal portion of the needle hub has a non-conventional configuration that allows it to mate only with a counterpart special connector of a fluid conveying device that has a complementary non-conventional configuration.

Description

CROSS REFERENCES TO RELATED APPLICATIONS

This application is a continuation-in-part application of application Ser. No. 13/567,122 filed on Aug. 6, 2012.

FIELD OF THE INVENTION

The present invention relates to needle assemblies, and particularly to a needle assembly that has a specially designed hub that enables a user to firmly grasp and manipulate the needle for insertion to a patient. The connector end of the hub has a non-conventional configuration that prevents the needle hub from connecting to conventional counterpart connectors.

BACKGROUND OF THE INVENTION

Some of the prior art spinal and epidural needles tend to be somewhat difficult to manipulate by a surgeon or anesthesiologist, when inserting the needle into the patient. The prior art does disclose some needle hubs that have means for the user to grasp. Such prior art includes U.S. Pat. Nos. 6,027,480, D378,405, D421,119 and D469,870. However, those needle hubs do not provide means to prevent the user from inadvertently making contact with the needle or guide the insertion of the needle to the patient, or have a connector that prevents mis-connection. The instant invention needle assembly is an improvement of the prior art needle assembles.

SUMMARY OF THE PRESENT INVENTION

The needle assembly of the instant invention has a needle hub that has a main body having a distal portion with a closed distal end to which a needle extends and a proximal portion to which there is an opened proximal end for connection to a fluid store such as a syringe or a fluid line. The body is a substantially cylindrical body with the distal portion sloping downwards from where it merges with the proximal portion towards the closed distal end. Two substantially rectangular plates are formed on opposite sides of the body that bridges the proximal and distal portions. The plates are bonded to the body in a parallel relationship, with the respective upper edges and the respective lower edges being substantially correspondingly coplanar. Accordingly, as the respective upper edges and respective lower edges of the two plates lie along corresponding planes, the needle hub, when placed onto a flat surface with either the respective upper edges or the respective lower edges, would stay put without rolling.
Proximate or adjacent to the two plates there is a partition at the distal portion of the needle hub body formed orthogonally to the longitudinal axis of the needle, and therefore orthogonal to the two plates that are bonded to opposite sides of the main body. The partition has its top edge in substantial coplanar alignment with the upper edges and its bottom edge in substantial coplanar alignment with respective lower edges of the two plates. As a result, upper and lower three point stable supports are provided by the respective edges of the two plates and the partition at their respective upper edges or their respective lower edges. This configuration ensures that when the needle assembly is put on a flat surface, it will not move due to unintentional rolling. In addition to providing additional support, the partition, being positioned at the distal portion of the needle hub, prevents the fingers of the user from inadvertently coming into contact with the needle that extends from the closed distal end.
There is a notch formed at the partition extending from its upper edge inwardly towards the body of the hub to provide a line of sight that extends to the bevel tip of the needle, which may include an orifice that opens on the side of the needle. The notch at the partition provides a line of sight from the needle tip to the space between the upper portion of the two plates which a user can use as a sight guide to insert the needle into the patient.
The opened proximal end of the needle hub forms the connector that connects the needle assembly to the fluid source. The proximal end is configured to have two protuberances that extend on opposite sides at the proximal portion of the body. In addition, the opening at the proximal end is configured such that the connector of the needle hub is matable only to a counterpart connector that has a complementary configuration. Also formed at the proximal end is a keyway that guides the insertion of a stylet into the needle to prevent the coring of the needle during its insertion into the patient.

BRIEF DESCRIPTION OF THE FIGURES

The present invention will become apparent and the invention itself will be best understood with reference to the following description of the present invention taken in conjunction with the accompanying drawings, wherein:

FIG. 1 is a top view of the needle assembly of the instant invention;

FIG. 2 is the bottom view of the inventive needle assembly;

FIG. 3 is one side view of the inventive needle assembly;

FIG. 4 is another side view of the inventive needle assembly;

FIG. 5 is a perspective front view of the inventive needle assembly;

FIG. 6 is a perspective rear view of the inventive needle assembly;

FIG. 7a is a perspective view of the needle assembly of the instant invention having the needle of a stylet partially inserted thereinto;

FIG. 7b is another perspective view of the needle assembly of the instant invention having inserted therein the needle of the stylet;

FIG. 8 is an illustration of the needle assembly of the instant invention, and other components that may be used in conjunction therewith;

FIG. 9 is another view of the needle hub shown in FIG. 4 amplified to illustrate the special non-conventional configuration at its connector end;

FIG. 10 is a semi-cross sectional view of the inventive needle assembly having a connector of a non-conventional configuration lockingly coupled to a syringe having a special counterpart connector;

FIG. 11 shows in perspective view a slip fit type needle hub of the needle assembly of the instant invention that has a non-conventional configuration; and

FIG. 12 is a perspective semi-cross sectional view of the needle hub of FIG. 10 fittingly mated to a special counterpart nose cone connector of a syringe.

DETAILED DESCRIPTION OF THE INVENTION

With reference to the figures, needle assembly 2 of the instant invention is shown to have a needle hub 4 that includes a distal portion 6 and a proximal portion 8. It should be appreciated that although designated as such in FIG. 2, there is no actual line of demarcation between distal portion 6 and proximal portion 8. Distal portion 6 has a closed distal end 6 a, whereas proximal portion 8 has an opened proximal end 8 a. Needle hub 4 has a main body 4 a that is substantially cylindrical along proximal portion 8 and slopes or inclines downwards in a conical fashion towards distal end 6 a along distal portion 6.
Two flats or plates 10 a and 10 b are bonded to body 4 a bridging distal portion 6 and proximal portion 8. Plates 10 a and 10 b each are substantially rectangular in shape, with their respective upper edges 10 a 1, 10 b 1 and their respective lower edges 10 a 2 and 10 b 2, slightly curved inwardly to form a slight concave configuration. For the instant invention, the respective upper edges 10 a 1 and 10 b 1 of plates 10 a and 10 b are deemed to lie substantially co-planarly along an upper plane, designated by dotted line 18 in FIG. 3; and the respective lower edges 10 a 2 and 10 b 2 of plates 10 a and 10 b are deemed to lie substantially co-planarly along a lower plane, designated by dotted line 20 in FIG. 3. Thus, the respective upper edges form one rest support for the needle hub, if the needle hub were to be placed on a flat surface using the respective upper edges 10 a 1 and 10 b 1. Likewise, the respective lower edges 10 a 2 and 10 b 2 form another rest support whereby the needle can be placed onto a flat surface by using those edges. Once placed onto a flat surface, the respective upper and lower edges each provide support for the needle hub, and prevent the needle hub from rolling. As best shown in FIGS. 1 and 2, plates 10 a and 10 b are formed in parallel to each other in a relationship that defines a space 10 c between the two plates.
At the closed distal end 6 a there is extending from needle hub 4 a needle 12. For the embodiment shown in the figures, needle 12 may be a spinal or epidural needle that has a closed end 12 a and a side opening or orifice 14 proximate to the closed end 12 a where through fluid from the needle may traverse. Although a needle with a closed end and a side orifice is shown, it should be appreciated that a spinal or epidural needle having an opened end tip is equally applicable for the instant invention.
At distal portion 6 between the respective front edges 10 a 3 and 10 b 3 of plates 10 a and 10 b and distal end 6 a there is integrally formed at needle hub 4 a partition plate, or simply a partition 16, orthogonally to the longitudinal axis 22 of the needle assembly. Partition 16 therefore is orthogonal to plates 10 a and 10 b, and provides a stop for the fingers (defined to include the thumb) of a clinician user, if the user is grasping plates 10 a and 10 b with his fingers, for example with his thumb and fore finger. As partition 16 prevents the fingers of the user from inadvertently making contact with needle 16, plates 10 a and 10 b prevent the needle from rolling between the fingers of the clinician user to ensure that the orientation of the tip of the needle may continuously be monitored by the user.
Partition 16 is substantially rectangular and has an upper edge 16 a and a lower edge 16 b. As best shown in FIG. 3, upper edge 16 a of plate 16 lies in a coplanar relationship with edges 10 b 1 and 10 a 1 of plates 10 b and 10 a, respectively, along plane 18. Similarly, the lower edge 16 b of partition 16 lies co-planarly with respective lower edges 10 a 2 and 10 b 2 of plates 10 a and 10 b along plane 20. See FIGS. 3 and 4. As a result, top edge 16 a of partition 16 and top edges 10 a 1 and 10 b 1 of plates 10 a and 10 b together form a multiple point stable support for the needle hub 4, were the needle hub to be rested on a flat surface by means of those edges. Likewise, bottom edge 16 b of partition 16 and respective bottom edges 10 a 2 and 10 b 2 of plates 10 a and 10 b together provide a multiple point stable support to ensure that the needle hub would not move once it has been placed onto a flat surface supported by those lower edges.
Partition 16 has a notch 16 b that extends from its top edge 16 a inwardly towards the longitudinal axis 22. Notch 16 is formed such that it provides a line of sight from needle tip 12 a to space 10 c defined between plates 10 a and 10 b at the top portion of the needle hub. Notch 16 b may act as a sight guide for the user to ensure that the bevel end of the needle, and/or also the side orifice 14, be correctly inserted into the patient. By grasping plates 10 a and 10 b with his thumb and fore finger and biasing the front portions of those digits against the side of partition 16 that faces plates 10 a and 10 b, the user can readily manipulate the needle since the rolling of the needle between the fingers of the user is prevented as discussed above. And by using partition 16 as a push plate, with the aid of notch 16 b, the orientation of the tip of the needle is continuously monitored as the user guidedly inserts the needle into the patient, so as to ensure the correct placement of the tip of the needle in the patient.
The connector of needle hub 4 is provided at the end of proximal portion 8 close to the opened proximal end 8 a. As shown, two protuberances 24 a and 24 b are provided at opposite sides of the connector at proximal portion 8. The protuberances are configured such that they are engagable only with a counterpart connector that has complementary channels or grooves for accepting them. Also, the opening 26 (FIG. 6) at proximal end 8 a has a dimension that allows the connector to only mate with a counterpart non-conventional connector that has a complementary dimensioned opening, so that needle hub 4 will not connect to a counterpart connector that has a conventional luer connector defined by International Standard Organization (ISO) standards. The dimension(s) of an exemplar non-conventional connecter that may be used for the connector portion of the needle assembly of the instant invention may be gleaned from co-pending application 61/457,879 (Atty Docket No. 0109/0037) filed on Jun. 27, 2011. The disclosure of the '879 application is incorporated by reference to the disclosure of the instant application.
A keyway 28 that extends from proximal end 8 a inwardly to body 4 a along the longitudinal axis 22 provides a guide, at proximal portion 8, for accepting a stylet 30 (FIGS. 7a and 7b ) that includes a stylet needle 30 a and its hub 30 b. As shown, stylet hub 30 b has a finger 30 c that slidably fits into keyway 28, when stylet hub 30 b is fitted to the connector portion of needle hub 4. There are also slots 30 b, only one being shown, that allows stylet hub 30 b to fit onto proximal portion 8 without interference from protuberances 24 a and 24 b. With stylet 30 fully inserted into hub 4, per shown in FIG. 7b , side orifice 14 of needle 12, per shown in the exploded view 32 of FIG. 7b , is blocked by stylet needle 30 a, so that there would not be any coring by needle 12, when needle 12 is inserted into the patient. Once the needle is properly placed within the patient, stylet 30 is removed, so that medicament may be conveyed to the patient by means of side orifice 14 of needle 12. In the case of an open ended spinal needle, the stylet blocks the opened end of the needle while it is inserted in the needle. It should be appreciate that even though a spinal needle is shown by the figures, an epidural needle (which has an opened end tip) may also be fitted with the inventive needle hub disclosed herein.
FIG. 8 shows the various components that may be used with the needle assembly 2 of the instant invention. As shown, there is a syringe 36 provided with a receptacle end 36 a having a configuration complementary to the connector portion of needle hub 4. A cap 38 that has a connector portion 38 a having a configuration similar to the connecter portion of needle hub 4 is provided to cap the receptacle end 36 a of syringe 36, prior to its use, so as to prevent possible contamination thereof. Syringe 36 may be used with a filter needle 34 that has a connector portion 34 a dimensionally configured to be connectable to receptacle end 36 a of syringe 36.
In use, cap 38 is removed from syringe 36. Needle 34 is then connected to syringe 36 so that medicament may be withdrawn from a vial (not shown) via needle 34 into syringe 36. Thereafter, needle 34 is discarded. Prior to or after the medicament has been withdrawn from the vial into syringe 36, the surgeon or anesthesiologist would insert the needle 12 of needle assembly 2 into the patient, for example spinally or epidurally. Once the needle 12 is correctly positioned in the patient, and after syringe 36 is filled with the appropriate medicament, needle hub 4 and syringe 36 are matingly coupled together so that the medicament stored in the syringe may be conveyed into the patient, in a manner well known in the art for example by pushing the plunger of the syringe. Although FIG. 8 illustrates one exemplar embodiment procedure for utilizing the needle assembly, it should be appreciated that the needle assembly of the instant invention may be an epidural needle having a connector for connection with a syringe for injection, or an epidural needle utilized to place an epidural catheter into the patient, with the epidural catheter connected to a fluid store such as a fluid line or a fluid cassette after the removal of the epidural needle as is well known in the art. The medicament may then be dispensed through the catheter to the patient by a syringe or an infusion pump.
With reference to FIG. 6 and the relevant disclosure form the above-noted incorporated by reference application No. 61/457,879, now application Ser. No. 13/517,782 filed on Jun. 14, 2012, the exemplar needle hub 4 has a female connector at its proximal end 8 that has a given or particular dimension(s), feature(s) and/or configuration that allows it to be connected to a counterpart connector such as the male connector 36 a of syringe 36 (FIG. 8) that has a complementary dimension(s), feature(s) and/or configuration to the proximal portion 8 of needle hub 4 of the needle assembly 2. Connector 36 a is an integral extension of syringe 36. Thus, male connector 36 a, which includes a nose cone extension to be discussed further with reference to FIG. 10, and the female connector at needle hub 4 have complementary features, dimensions and/or configurations that allow those connectors to matingly coupled, connected or fitted to each other, but not with standard connectors such as luer connectors that have conventional configurations manufactured in accordance with ISO (International Standard Organization) Standards 591-1 and 594-2. For ease of discussion, henceforth it should be assumed that the term “configuration” is inclusive of the dimensions and other features of the being discussed connectors that either enable or prevent those connectors and their counterparts (male and female) from matingly connect or couple to each other.
The needle hub 4 shown in FIG. 6 is reproduced in a semi-see-through view of FIG. 9. As shown, the proximal portion 8 of needle hub 4 has an elongate substantially cylindrical body, represented by main body 4 a that has an opening 26 at its proximal end 8 b. The elongate body 4 a has two bosses or protrusions 24 a and 24 b extending from opposite sides of its outer surface 4 a 1. Opening 26 forms the mouth of a through bore 27 that extends into body 4 a. Although not shown, as is well known, bore 27, possibly reduced in diameter, extends throughout the rest of the needle hub 4 to meet with the cannula of needle 4 so that a through passage extends from opening 26 to the close end 6 a at the distal end of the distal portion 6 of hub 4, and from there establishing a passageway with needle 12 (FIGS. 1 and 2) that extends to the tip of the needle.
Further with reference to FIG. 9, through bore 27 is shown to be tapered and defined by a circumferential wall 4 b whose inner circumferential surface 4 b 1 forms a cross-sectional dimension that has a decreasing conical cross-section from opening 26 to the distal opening 26 a proximately at the end of proximal portion 8. The exemplar dimensions for the non-conventional configuration at the proximal portion 8 of needle hub 4 may be referenced with respect to the above noted application Ser. No. 13/517,782, and will be discussed in greater detail relative to the special connector or connector fitting of a fluid conveying device, for example syringe 36 shown in FIG. 8, that has a counterpart complementary configuration to the non-conventional configuration of needle hub 4. The connector fitting of needle hub 4 shown in FIG. 9 may be referred to as a lock type connector due to protrusions 24 a and 24 b extending from its outer circumferential surface.
With reference to FIG. 10, the exemplar syringe 36 illustrated in FIG. 8 is shown to be lockingly coupled to the lock type needle hub 4 shown in FIG. 9. In particular, syringe 36 has a connector fitting 36 a that is a special connector having a counterpart configuration that is complementary to the non-conventional configuration at proximal portion 8 of needle hub 4. As shown, special connector 36 a includes a circumferential wall 36 a 1 that integrally extends from the body 39 of syringe 36. Also extending from the distal end of body 36 is a tapered nose cone or nose cone extension 36 c having a through bore 40 that extends from its distal end 36 d into chamber 42 of syringe 36. Nose cone extension 36 d is surrounded or circumscribed by wall 36 a 1, which has two spiral grooves 36 b 1 and 36 b 2 at its inner surface with corresponding openings at distal end 36 d formed to accept protrusions 24 a and 24 b, respectively, of hub 4. When syringe 36 is coupled to needle hub 4, a through passage is established between chamber 42 and bore 27 of hub 4 via bore 40.
The nose 36 c 1 of nose cone extension 36 c is configured to have a cross-section that is slightly smaller than cross-section 26 a of opening 26 of hub 4, so that nose cone extension 36 c is readily insertable through opening 26. Moreover, the outer wall 36 c 2 of tapered nose cone extension 36 c is configured to have an increasing conical cross-section from nose 36 c 1 that complements with the decreasing conical configuration of counter-tapered bore 27 of needle hub 4, so that nose cone extension 36 c can fittingly insert into bore 27 of hub 4 to prevent fluid leak from bore 27. Furthermore, with protrusions 24 a and 24 b of hub 4 threadingly mated to their corresponding grooves 36 b 1 and 36 b 2, needle hub 4 and special connector 36 a of syringe 36 are lockingly coupled to each other. As was discussed above, given that needle hub 4 has a non-conventional configuration and special connector 36 c of syringe 36 has a configuration that is complementary to the non-conventional configuration of needle hub 4, the respective connectors of needle hub 4 and syringe 36 each are not connectable to counterpart conventional connector fittings.
FIG. 11 shows a slip fit type connector of the instant invention that has a non-conventional configuration. The non-conventional configuration slip fit connector 4 may have the same components and dimensions as the lock type connector shown in FIG. 9 but without the bosses or protrusions 24 a and 24 b. Thus, the needle hub 4 of FIG. 11 is fittingly matable to syringe 36 solely by the mating of nose cone extension 36 c into bore 27 at the proximal portion 8 of hub 4. Same as the lock type connector discussed above, the outer circumferential wall 36 c 2 of nose cone extension 36 c and the inner circumferential wall 4 b 1 of the proximal portion 8 that defines bore 27 are configured to have complementary conical increasing/decreasing (or tapered/counter-tapered) configurations that enable nose cone extension 36 c to form fittingly slide fit into bore 27 and be frictionally held thereat to establish a fluid tight connection, so that medicament fluid may be conveyed from syringe 36 to the needle extending from needle hub 4.
Note that although circumferential wall 36 a 1 that circumscribes nose cone extension 36 c is shown in FIG. 12, in practice, a circumferential wall is not needed fora slip fit type syringe. Furthermore, as shown in FIG. 12, the slip type connector fitting of hub 4 may also be used with a lock type syringe insofar as proximal portion 8 of the connector has a cross-sectional dimension that is slightly smaller than the cross-sectional dimension of the inner circumferential wall 36 a 1′ of the outer wall 36 a 1. Thus, per shown in FIG. 12, the inner circumferential wall 4 b 1 of the needle hub connector and the outer circumferential wall 36 c 2 of the nose cone extension 36 c may be frictionally mated to each other, while the outside circumferential wall 4 b 2 at the proximal portion 8 of the needle hub and the inner circumferential wall 36 a 1′ of the circumferential wall 36 a 1 of connector 36 a are not in contact with each other, when the slip fit type connector of FIG. 11 is mated to a locked type syringe 36.
Exemplar dimensions of the inventive connectors may be as follows. Opening 26 of the inventive connector 4, shown for example to be female in FIG. 9, has been configured with a taper from approximately 4% to 6%, preferably approximately 5% or 3° (3 degrees), as compared to a taper of 6% or 3.44° for the conventional luer female connectors manufactured under the afore-noted ISO standards. As a result, a conventional male luer connector produced in accordance with the afore-noted ISO standards that otherwise mates readily with a conventional female luer connector could not mate with the inventive female connector, as the configuration of the conventional male luer connector is not complementary to the configuration of the inventive female connector. This is due to the opening 26 and the bore 27 tapering therefrom being configured not to accept the fitting of a conventional luer male connector. There may be other configurations, for example the cross-sectional dimension or the width 26 a of the mouth of opening 26, or the thickness of the wall 4 b of the connector that would prevent the inventive female connector of hub 4 from mating with a counterpart male luer connector of a conventional configuration.
With reference to FIGS. 10 and 12, the exemplar special male connector 36 c is shown to have a nose cone extension or nose portion 36 c that has a taper from approximately 4% to 6%, preferably 5% or 3° outwards complement to that of the approximately 5% or 3° inward taper of the counter exemplar bore 27 of the female connector of hub 4 discussed above. Also, the outer circumferential wall 36 c 2 of nose cone extension 36 c has a width that is slightly smaller than the width for the inner circumferential surface 4 b 1 of the mating portion 4 a of the female connector 4, so that nose cone extension 36 c can readily fit into the bore 27 of the female connector. The respective widths of the circumferential wall of cone extension 36 c and the inner circumferential surface of mating portion 4 a of female connector 4 of the instant invention may be dimensioned to be different from (preferably smaller than but could be greater than) those widths or cross sections of the conventional luer connectors noted above so as to act as another feature that prevents the inventive non-conventional configuration connectors from mating to counterpart connectors of conventional configurations.
Inasmuch as the present invention is subject to many variations, modifications and changes in detail, it is intended that the matter described throughout this specification and shown in the accompanying drawings be interpreted as illustrative only and not in a limiting sense. Accordingly, it is intended that the invention be limited only by the spirit and scope of the hereto appended claims.

Claims

1-20. (canceled)

21. A needle assembly, comprising:

a needle hub including a main body extending along a longitudinal axis having an open proximal end and a closed distal end;

a needle having a distal tip including an aperture and a proximal end connected to the closed end of said hub to establish a through passage between the aperture of the needle and the open end of the hub;

wherein said hub includes two plates positioned at opposite sides of the main body, said plates each having an upper edge and a lower edge, the upper and lower edges of each of said plates slightly curved inwardly to form a concave configuration for each plate, said two plates bonded along the main body in parallel to each other, the respective top edges of said two plates lying substantially co-planarly along an upper plane and the respective bottom edges of said two plates lying substantially co-planarly along a lower plane so that the respective top edges form one rest support and the respective bottom edges form another rest support for said needle hub when said needle hub is placed onto a flat surface using the respective top edges or the respective lower edges of said two plates.

22. The needle assembly of claim 21, further comprising a partition positioned orthogonal to and separating said two plates from the closed distal end of said hub whereto the proximal end of the needle is connected.

23. The needle assembly of claim 22, wherein said partition is substantially rectangular and has an upper and a lower edge, the upper edge of said partition lies in a coplanar relationship with the respective upper edges of said two plates and the lower edge of said partition lies in a coplanar relationship with the respective lower edges of said two plates, so that the upper edges of said partition and said two plates form a stable multiple edge support for said needle hub and the lower edges of said partition and said two plates form another stable multiple edge support for said needle hub.

24. The needle assembly of claim 21, wherein said needle hub comprises a proximal portion that includes a substantially cylindrical body having an outer surface and two protrusions extending from opposite sides of the outer surface at or proximate to the proximal end to engage with a counterpart connector of a fluid conveying device.

25. The needle assembly of claim 29, wherein the fluid conveying device comprises a syringe, a fluid line or a fluid store.

26. The needle assembly of claim 21, wherein the needle comprises a spinal or epidural needle.

27. The needle assembly of claim 21, further comprising a notch at said hub to provide a line of sight from the distal tip of the needle to a space defined between said two plates to guide a user to correctly insert the bevel end of the needle into the patient.

28. The needle assembly of claim 27, wherein the notch extends from a top edge of said partition.

29. A needle assembly comprising:

a needle hub including a body extending along a longitudinal axis having an open proximal end and a distal portion including a closed distal end;

a needle extending from the closed distal end; and

two plates bonded to opposite sides of the body in parallel to each other, said two plates each having a top edge and a bottom edge, each of the top and bottom edges of said two plates slightly curved inwardly to form a concave configuration so that the two ends of the respective top edges of said two plates lie substantially co-planarly along an upper plane to form one rest support and the two ends of the respective bottom edges of said two plates lie substantially co-planarly along a lower plane to form another rest support.

30. The needle assembly of claim 29, further comprising:

a partition bonded to said body orthogonal to said two plates, said partition having a top edge that lies substantially coplanarly along the upper plane and a bottom edge that lies substantially coplanarly along the lower plane so that the ends of the top edges of said two plates and the top edge of said partition form a multiple edge top support and the ends of the bottom edges of said two plates and the bottom edge of said partition form a multiple edge bottom support for said needle hub when said needle hub is placed onto a flat surface using the respective top edges or the respective bottom edges.

31. The needle assembly of claim 29, wherein the body of said hub comprises a substantially cylindrical body having an outer surface and an opening at the proximal end to a bore through the cylindrical body, two protrusions extending from opposite sides of the outer surface proximate to or at the proximal end to engage with a counterpart connector of a fluid conveying device.

32. The needle assembly of claim 29, wherein the fluid conveying device comprises a syringe, a fluid bag, a fluid line or a fluid cassette.

33. The needle assembly of claim 29, wherein the needle comprises a spinal or an epidural needle.

34. The needle assembly of claim 30, further comprising a notch at said hub to provide a line of sight from the distal tip of the needle to a space defined between said two plates to guide a user to correctly insert the bevel end of the needle into the patient.

35. The needle assembly of claim 34, wherein the notch extends from a top edge of said partition.

36. A method of manufacturing a needle assembly, comprising:

providing a needle hub including a body extending along a longitudinal axis having an open proximal end and a distal portion including a closed distal end;

extending a needle from the closed distal end;

bonding two plates to opposite sides of the body in parallel to each other, said two plates each having a top edge and a bottom edge; and

configuring each of the top and bottom edges of said two plates slightly curved inwardly to form a concave configuration so that the two ends of the respective top edges of said two plates lie substantially co-planarly along an upper plane to form one rest support and the two ends of the respective bottom edges of said two plates lie substantially co-planarly along a lower plane to form another rest support.

37. The method of claim 36, further comprising:

bonding a partition to said body orthogonal to said two plates, said partition having a top edge that lies substantially coplanarly along the upper plane and a bottom edge that lies substantially coplanarly along the lower plane so that the ends of the top edges of said two plates and the top edge of said partition form a multiple edge top support and the ends of the bottom edges of said two plates and the bottom edge of said partition form a multiple edge bottom support for said needle hub when said needle hub is placed onto a flat surface using the respective top edges or the respective bottom edges.

38. The method of claim 37, further comprising:

forming a notch at said hub to provide a line of sight from the distal tip of the needle to the space between said two plates to guide a user to correctly insert the bevel end of the needle into the patient.

39. The method of claim 38, further comprising:

forming the notch at a top edge of said partition.