Dual chamber syringe with retractable needle

Patent metadata

Field	Value
Publication number	US-12290669-B2
Application number	US-202217874955-A
Country	US
Kind code	B2
Filing date	Jul 27, 2022
Priority date	Jul 22, 2010
Publication date	May 6, 2025
Grant date	May 6, 2025

Abstract

Embodiments of a retractable syringe assembly are provided that include a dual syringe barrel configuration. One or more embodiments include reuse prevention features and features that prevent premature activation of the retraction mechanism. Methods for aspirating and expelling liquid from medical devices are also provided.

First claim

What is claimed is:

1. A syringe assembly comprising:
a fluid barrel including a sidewall having an inside surface defining a fluid chamber for retaining fluid and having a first cross-sectional width, an open proximal end and a distal end including a distal wall;
a plunger rod disposed within the fluid chamber comprising a distal end, a proximal end, a plunger rod body extending from the distal end of the plunger rod to the proximal end of the plunger rod, and a stopper disposed at the distal end of the plunger rod for forming a fluid-tight seal with the inside surface of the fluid barrel;
a retraction barrel disposed adjacent to the sidewall of the fluid barrel, the retraction barrel including a wall having an interior surface defining a needle chamber, an open proximal end, an open distal end including a barrier wall, an aperture between the wall of the retraction barrel and the sidewall of the fluid barrel permitting fluid communication between the fluid chamber and the needle chamber and a needle hub assembly comprising a needle hub, a needle cannula attached to the needle hub, the needle cannula being in fluid communication with the aperture and biased to move in a proximal direction; and
a trigger element disposed within the needle chamber and moveable within the retraction barrel independently from the plunger rod, the trigger element including a distal end and a proximal end, and a trigger element body that extends from the distal end of the trigger element to the proximal end of the trigger element, the trigger element providing a trigger force causing the needle cannula to retract into the retraction barrel, and a snap element disposed adjacent to the proximal end of the trigger element, the snap element including an angled surface, the snap element including a distal end and a proximal end; the angled surface of the snap element is configured to engage the retraction barrel for preventing distal movement of the trigger element, wherein the angled surface of the snap element has a height that increases from the proximal end of the snap element to the distal end of the snap element to permit or facilitate movement of the plunger rod past the snap element; the plunger rod includes a contacting surface as a flat radial ring that deflects the snap element allowing the trigger element to be moved in the distal direction to allow the retraction of the needle cannula.

2. The syringe assembly of claim 1 , wherein the inside surface of the fluid chamber sidewall includes a retaining ring adjacent to the proximal end of the fluid barrel defining a second cross-sectional width that is less than the first cross-sectional width and the plunger rod body includes a flexible protrusion having a cross-sectional width greater than a cross-sectional width of the fluid barrel at a rib and a frangible portion.

3. The syringe assembly of claim 2 , wherein contact between the stopper and the distal wall of the fluid barrel causes the protrusion to advance distally past the rib in the fluid barrel and lock the plunger rod in the fluid barrel to prevent reuse of the syringe assembly.

4. The syringe assembly of claim 3 , wherein continuous application of a force on the plunger rod in the proximal direction after the protrusion has advanced distally past the rib causes the frangible portion to break.

5. The syringe assembly of claim 2 , wherein the distal end of the plunger rod includes a stopper-engaging portion and the stopper is attached to the stopper-engaging portion of the plunger rod, the stopper being distally and proximally movable relative to the stopper-engaging portion for a pre-selected axial distance such that when a force is applied to the plunger rod in a distal direction and a distal end of the stopper is in contact with the distal wall of the fluid barrel, the protrusion is permitted to advance distally past the rib in the fluid barrel and lock the plunger rod in the fluid barrel to prevent reuse of the syringe assembly.

6. The syringe assembly of claim 5 , wherein continuous application of a force on the plunger rod in the proximal direction after the protrusion has advanced distally past the rib causes the frangible portion to break.

7. The syringe assembly of claim 1 , wherein engagement of the snap element with the retraction barrel applies a force on the snap element in the proximal direction, preventing the snap element from depressing and hindering movement of the trigger element in the distal direction.

8. The syringe assembly of claim 1 , wherein the snap element is rotatable.

9. The syringe assembly of claim 1 , wherein the retraction barrel includes a first locking element which engages with a second locking element disposed on the trigger element body.

10. The syringe assembly of claim 9 , wherein the first locking element is in the form of an opening on the wall of the retraction barrel.

11. The syringe assembly of claim 9 , wherein the second locking element is in the form of an outwardly extending projection disposed on the trigger element body.

12. The syringe assembly of claim 11 , wherein the outwardly extending projection includes a proximally facing stop face.

13. A method comprising:
providing the syringe assembly of claim 1 ;
providing instructions to:
submerge an opening of the needle cannula in a liquid;
fill the fluid barrel with the liquid by applying a force to the plunger rod in a proximal direction;
expel the liquid from the fluid barrel by applying a force to the plunger rod in a distal direction; and
retract the needle cannula into the retraction barrel by applying a force to the trigger element in the distal direction to provide the trigger force.

14. The method of claim 13 , further comprising providing instructions to lock the plunger rod in the fluid barrel after expelling the liquid from the fluid barrel.

15. The method of claim 13 , wherein the force applied to the plunger rod is oriented along an axis that is parallel to an axis along which the force applied to the trigger element is oriented.

16. The method of claim 13 , the force applied to the plunger rod to expel the liquid is less than the force applied to the trigger element.

Assignees

• Becton Dickinson Co

Inventors

• Zivkovic Ivan
• Hager Jorgen
• Handberg Ulf
• Hanner Gert
• Holma Thomas
• Wahlberg Ulf

Classifications

• A61M2205/586

  Ergonomic details therefor, e.g. specific ergonomics for left or right-handed users · CPC title

• A61M2205/583

  by visual feedback · CPC title

• A61M2205/582

  by tactile feedback · CPC title

• A61M2005/5033

  by use of an intermediate blocking member positioned between the syringe barrel and the piston rod to prevent retraction of the latter, e.g. toothed clip placed on the piston rod · CPC title

• A61M2005/3139

  Finger grips not integrally formed with the syringe barrel, e.g. using adapter with finger grips · CPC title