Needle sheath assembly

Claim 2

A hypodermic syringe assembly comprising: an elongate barrel having an open proximal end, a chamber for retaining fluid and a tip portion extending from a distal end of said barrel having a passageway therethrough communicating with said chamber; a needle cannula having a distal end extending outwardly from said tip portion including a lumen therethrough in fluid communication with said passageway; a needle shield assembly including a resilient needle sheath having an open proximal end, a closed distal end, a sidewall defining a receptacle therein, said resilient needle sheath being positioned within an elongate rigid needle shield having an open proximal end, a closed distal end and a sidewall therebetween; means for holding said sheath within said shield so that said sheath cannot be removed from said shield during normal use of said syringe assembly, said sheath including cannula sealing means at said distal end of said receptacle for providing a fluid-tight seal between said lumen and the environment of said syringe assembly; said needle shield assembly being positioned with said distal end of said cannula engaging said cannula sealing means and said proximal end of said sheath removably engaging said tip portion to hold said shield assembly on said barrel while simultaneously sealing said lumen of said cannula so that said sheath surrounds the entire portion of said cannula which extends outwardly from said tip portion; said shield and said sheath being structured so that said shield cannot be manually assembled to or manually separated from said sheath while said sheath is properly positioned sealing said cannula and engaging said tip portion of said barrel; and said needle shield assembly being easily engageable to and removable from said barrel and said cannula using manual force applied to said shield.

Claim 3

The hypodermic syringe assembly of claim 1 wherein said cannula sealing means includes an elongate retention conduit having a sidewall adapted to accept said distal end of said cannula in fluid-tight engagement between the outside of said cannula and said conduit sidewall.

Claim 4

The hypodermic syringe assembly of claim 2 wherein said retention conduit includes a circularly shaped cross section portion having a diameter which is less than the outside diameter of said cannula.

Claim 5

The hypodermic syringe assembly of claim 1, wherein said sealing means includes said cannula being long enough so that when said needle shield assembly is positioned on said tip portion said distal end of said cannula is embedded in said closed distal end of said sheath with portions of said sheath occluding said lumen.

Claim 6

The hypodermic syringe assembly of claim 1 wherein said needle sheath includes a projection extending outwardly from its proximal end, and said means for holding said sheath within said shield including a first inwardly projecting ledge, in said shield, positioned proximally of said sheath projection.

Claim 7

The hypodermic syringe assembly of claim 5 wherein said holding means further includes a second inwardly projecting ledge, in said shield, positioned distally of said sheath projection.

Claim 8

The hypodermic syringe assembly of claim 5 wherein said sheath projection is an annular flange positioned at said proximal end of said sheath.

Claim 9

The hypodermic syringe assembly of claim 6 wherein said inwardly projecting ledges are annular inwardly projecting shoulders.

Claim 10

The hypodermic syringe assembly of claim 5 wherein said shield comprises a distal member including said first inwardly projecting ledge and a proximal member including said second inwardly projecting ledge, said proximal member and said distal member being joined together to form said shield.

Claim 11

The hypodermic syringe assembly of claim 1 wherein said shield includes an aperture in said distal end allowing fluid communication between portions of the exterior of said sheath and the environment of said syringe assembly.

Claim 12

The hypodermic syringe assembly of claim 1 further including a stopper slidably positioned in fluid-tight engagement inside said barrel adapted to engage a plunger rod to facilitate its operation, said stopper capable of moving fluid from said chamber through said passageway upon its movement toward said distal end, said stopper capable of facilitating the drawing of fluid into said chamber through said passageway upon its movement away from said distal end.

Claim 13

The hypodermic syringe assembly of claim 11 further including medicament within said chamber between said stopper and said distal end of said barrel.

Claim 14

The hypodermic syringe assembly of claim 11 further including a plunger rod engaged to said stopper and extending outwardly from said proximal end of said barrel.

Claim 15

The hypodermic syringe assembly of claim 1 wherein said sheath is made from material selected from the group consisting of natural rubber, synthetic rubber and thermoplastic elastomers.

Claim 16

The hypodermic syringe assembly of claim 1 wherein said shield is made of rigid material selected from the group consisting of thermoplastic, thermosetting plastic, metals and combinations thereof.

Claim 17

The hypodermic syringe assembly of claim 1 wherein said barrel is made of glass.

Claim 18

A hypodermic syringe assembly comprising a barrel having an open proximal end, a chamber for retaining fluid and a tip portion extending from a distal end of said barrel having a passageway therethrough communicating with said chamber; a needle cannula having a distal end extending outwardly from said tip portion including a lumen therethrough in fluid communication with said passageway; a needle shield assembly including a resilient needle sheath having an open proximal end, a closed distal end, a sidewall defining a receptacle therein, said resilient needle sheath being positioned within an elongate rigid needle shield having an open proximal end; a distal end and a sidewall therebetween; means for holding said sheath within said shield so that said sheath cannot be removed from said shield during normal use of said syringe assembly, said sheath including cannula sealing means at said distal end of said receptacle; said needle shield assembly being positioned with said distal end of said cannula engaging said cannula sealing means and said proximal end of said needle sheath removably engaging said tip portion to hold said shield assembly on said barrel while simultaneously sealing said lumen of said cannula so that said sheath surrounds the entire portion of said cannula which extends outwardly from said tip portion.

Claim 19

A hypodermic syringe assembly comprising a barrel having an open proximal end, a chamber for retaining fluid and a tip portion extending from a distal end of said barrel having a passageway therethrough communicating with said chamber; a needle cannula having a distal end extending outwardly from said tip portion including a lumen therethrough in fluid communication with said passageway; a needle shield assembly including a resilient needle sheath having an open proximal end, a closed distal end, a sidewall defining a receptacle therein, said resilient needle sheath being positioned within an elongate rigid needle shield having an open proximal end; a distal end and a sidewall therebetween; means for holding said sheath within said shield so that said sheath cannot be removed from said shield during normal use of said syringe assembly, said sheath including cannula sealing means at said distal end of said receptacle; said needle shield assembly being positioned with said distal end of said cannula engaging said cannula sealing means and said proximal end of said needle sheath removably engaging said tip portion to hold said shield assembly on said barrel while simultaneously sealing said lumen of said cannula so that said sheath surrounds the entire portion of said cannula which extends outwardly from said tip portion.

Claim 20

A hypodermic syringe assembly comprising an elongate barrel having an open proximal end, a chamber for retaining fluid and a tip portion extending from a distal end of said barrel having a passageway therethrough communicating with said chamber; a needle cannula having a distal end extending outwardly from said tip portion including a lumen therethrough in fluid communication with said passageway; a needle shield assembly including a resilient needle sheath having an open proximal end, a closed distal end, a sidewall defining a receptacle therein, a projection extending outwardly from said proximal end, said resilient needle sheath being positioned within an elongate rigid shield having an open proximal end, a distal end and a sidewall therebetween; means for holding said sheath within said shield so that said sheath cannot be removed from said shield during normal use of said syringe assembly, said holding means including a first inwardly projecting ledge in said shield positioned proximally of said sheath projection; said sheath including cannula sealing means at said distal end of said receptacle for providing a fluid-tight seal between said lumen and the environment of said syringe assembly including an elongate retention conduit having a sidewall adapted to accept said distal end of said cannula in fluid-tight engagement between the outside of said cannula and said conduit sidewall; said needle shield assembly being positioned with said distal end of said cannula engaging said cannula sealing means and said proximal end of said sheath removably engaging said tip portion to hold said needle shield assembly on said barrel while simultaneously sealing said lumen of said cannula so that said sheath surrounds the entire portion of said cannula which extends outwardly from said tip portion, said shield and said sheath being structured so that said shield cannot be manually assembled to or manually separated from said sheath while said sheath is properly positioned sealing said cannula and engaging said tip portion of said barrel; said needle shield assembly being easily engageable to and removable from said barrel and said cannula using manual force applied to said shield; a stopper slidably positioned in fluid-tight engagement inside said barrel adapted to engage a plunger rod to facilitate its operation, said stopper capable of moving fluid from said chamber through said passageway upon its movement toward said distal end, said stopper capable of facilitating the drawing of fluid into said chamber through said passageway upon its movement away from said distal end; and medicament within said chamber between said stopper and said distal end of said barrel.

Claim 21

A hypodermic syringe assembly comprising an elongate barrel having an open proximal end, a chamber for retaining fluid and a tip portion extending from a distal end of said barrel having a passageway therethrough communicating with said chamber; a needle cannula having a distal end extending outwardly from said tip portion including a lumen therethrough in fluid communication with said passageway; a needle shield assembly including a resilient needle sheath having an open proximal end, a closed distal end, a sidewall defining a receptacle therein, a projection extending outwardly from said proximal end, said resilient needle sheath being positioned within an elongate rigid shield having an open proximal end, a distal end and a sidewall therebetween; means for holding said sheath within said shield so that said sheath cannot be removed from said shield during normal use of said syringe assembly, said holding means including a first inwardly projecting ledge in said shield positioned proximally of said sheath projection; said sheath including cannula sealing means at said distal end of said receptacle for providing a fluid-tight seal between said lumen and the environment of said syringe assembly including an elongate retention conduit having a sidewall adapted to accept said distal end of said cannula in fluid-tight engagement between the outside of said cannula and said conduit sidewall; said needle shield assembly being positioned with said distal end of said cannula engaging said cannula sealing means and said proximal end of said sheath removably engaging said tip portion to hold said needle shield assembly on said barrel while simultaneously sealing said lumen of said cannula so that said sheath surrounds the entire portion of said cannula which extends outwardly from said tip portion, said shield and said sheath being structured so that said shield cannot be manually assembled to or manually separated from said sheath while said sheath is properly positioned sealing said cannula and engaging said tip portion of said barrel; said needle shield assembly being easily engageable to and removable from said barrel and said cannula using manual force applied to said shield; a stopper slidably positioned in fluid-tight engagement inside said barrel adapted to engage a plunger rod to facilitate its operation, said stopper capable of moving fluid from said chamber through said passageway upon its movement toward said distal end, said stopper capable of facilitating the drawing of fluid into said chamber through said passageway upon its movement away from said distal end; and medicament within said chamber between said stopper and said distal end of said barrel.

Claim 22

The hypodermic syringe assembly of claim 18 wherein said holding means further includes a second inwardly projecting ledge in said shield positioned distally of said sheath projection.

Claim 23

The hypodermic syringe assembly of claim 18 wherein said sheath projection is an annular flange positioned at said proximal end of said sheath and said first inwardly projecting ledge is an annular inwardly projecting shoulder.

Claim 24

A needle shield assembly for use with a syringe barrel having a chamber for retaining fluid, a tip portion extending outwardly from a distal end of said barrel having a passageway therethrough and a needle having a distal end extending outwardly from said tip portion having a lumen therethrough in fluid communication with said passageway comprising: a resilient needle sheath having an open proximal end, a closed distal end, a sidewall defining a receptacle therein, and a projection extending outwardly from said proximal end; said resilient needle sheath being positioned within an elongate rigid shield having an open proximal end, a closed distal end and a sidewall therebetween; means for holding said sheath within said shield so that said sheath cannot be removed from said shield during normal use of said syringe assembly including a first inwardly projecting ledge in said shield, positioned proximally of said sheath projection; said sheath including cannula sealing means at said distal end of said receptacle for providing a fluid-tight seal between said lumen and the environment of said syringe assembly; said needle shield assembly being sized so that said distal end of said cannula sealing means is adapted to engage said cannula and said proximal end of said sheath is adapted to removably engage said tip portion to hold said shield assembly on said barrel while simultaneously sealing said lumen of said cannula so that said sheath may surround the entire portion of said cannula which extends outwardly from said tip portion; said shield and said sheath being structured so that said shield cannot be manually assembled to or manually separated from said sheath while said sheath is properly positioned sealing said cannula and engaging said tip portion of said barrel; and said needle shield assembly being easily engageable to and removable from said barrel and said cannula using manual force.

Claim 25

A needle shield assembly for use with a syringe barrel having a chamber for retaining fluid, a tip portion extending outwardly from a distal end of said barrel having a passageway therethrough and a needle having a distal end extending outwardly from said tip portion having a lumen therethrough in fluid communication with said passageway comprising: a resilient needle sheath having an open proximal end, a closed distal end, a sidewall defining a receptacle therein, and a projection extending outwardly from said proximal end; said resilient needle sheath being positioned within an elongate rigid shield having an open proximal end, a closed distal end and a sidewall therebetween; means for holding said sheath within said shield so that said sheath cannot be removed from said shield during normal use of said syringe assembly including a first inwardly projecting ledge in said shield, positioned proximally of said sheath projection; said sheath including cannula sealing means at said distal end of said receptacle for providing a fluid-tight seal between said lumen and the environment of said syringe assembly; said needle shield assembly being sized so that said distal end of said cannula sealing means is adapted to engage said cannula and said proximal end of said sheath is adapted to removably engage said tip portion to hold said shield assembly on said barrel while simultaneously sealing said lumen of said cannula so that said sheath may surround the entire portion of said cannula which extends outwardly from said tip portion; said shield and said sheath being structured so that said shield cannot be manually assembled to or manually separated from said sheath while said sheath is properly positioned sealing said cannula and engaging said tip portion of said barrel; and said needle shield assembly being easily engageable to and removable from said barrel and said cannula using manual force.

Claim 26

The needle shield assembly of claim 21 wherein said cannula sealing means includes an elongate retention conduit having a sidewall adapted to accept said distal end of said cannula in fluid-tight engagement between the outside of said cannula and said conduit sidewall.

Claim 27

The needle shield assembly of claim 21 wherein said holding means further includes a second inwardly projecting ledge in said shield positioned distally of said sheath projection.

Claim 28

The needle shield assembly of claim 21 wherein said sheath projection is an annular flange positioned at said proximal end of said sheath and said first inwardly projecting ledge is an annular inwardly directed shoulder.

Claim 29

The needle shield assembly of claim 23 wherein said shield comprises a proximal member including said first inwardly projecting ledge and a distal member including said second inwardly projecting ledge, said proximal member and said distal member being joined together to form said shield.

Claim 30

The needle shield assembly of claim 21 wherein said shield includes an aperture in said distal end allowing fluid communication between portions of the exterior of said sheath and the environment of said syringe assembly.

Claim 31

The needle shield assembly of claim 21 wherein said sheath is made of natural rubber.