IMPLANT SYRINGE

Abstract

An implant syringe includes a cannula, a storage element for receiving a solid material implant, and an outer sleeve with a radially projecting front gripping section which are axially movable together. An inner sleeve affords axial slits through which radial webs on the outer sleeve engage, and also includes a rod-shaped piston. The rod-shaped piston may be advanced through the storage element into the cannula such that a gap remains between the tip of the cannula and the head end of the piston. The cannula is rigidly connected to the storage element to form a cannula unit, that the webs on the outer sleeve are attached to an annular receiving member within the inner sleeve and that the cannula unit is insertable into the receiving member and is lockable therein, where a solid material implant can be inserted into the storage element.

Claims

1. An implant syringe comprising: a cannula, a storage element for receiving a solid material implant, an outer sleeve with a radially projecting front gripping section, with which the cannula, the storage element and the outer sleeve are together axially movable, an inner sleeve, on which the outer sleeve is located and in which the cannula is slidable with the storage element, wherein the inner sleeve affords axial slits, through which radial webs on the outer sleeve engage, further including a rod-shaped piston, which is fastened to a rear gripping section and is partially surrounded by a rear sleeve, which can slidably engage in the inner sleeve, wherein the rod-shaped piston may be advanced so far through the storage element into the cannula that a spacing remains between the tip of the cannula and the head end of the piston, which is approximately equal to the length of the solid material implant to be dispensed, wherein the outer sleeve is releasably locked in the advanced starting position with the cannula exposed by a blocking device on the inner sleeve and when the rear sleeve is advanced into its end position the blocking device is moved into the release position, whereby the outer sleeve is retractable by means of the front gripping section on the inner sleeve so that the cannula enters completely into the inner sleeve, wherein the cannula is rigidly connected to the storage element to form a cannula unit, that the radially inner ends of the webs on the outer sleeve are attached to an annular receiving member within the inner sleeve, and that the cannula unit is insertable into the receiving member and is lockable therein, whereby a solid material implant can be inserted into the storage element.

2. An implant syringe as claimed in claim 1, wherein the cannula is overmoulded with the storage element.

3. An implant syringe as claimed in claim 1, wherein the cannula is secured in the storage element by adhesive.

4. An implant syringe as claimed in claim 1, wherein the annular receiving member tapers conically in an insertion direction of the storage element.

5. An implant syringe as claimed in claim 1, wherein the insertion of the storage element into the receiving member is limited by a projection on the storage element.

6. An implant syringe as claimed in claim 1, wherein the storage element is unreleasably fixed in the end position of its insertion by at least one hook-shaped projection.

7. An implant syringe as claimed in claim 1, wherein a protective cap covering the cannula is positionable on the end section of the storage element, which may be slid into the inner sleeve with the storage element up to the radial webs on the outer sleeve.

8. An implant syringe as claimed in claim 7, wherein the protective cap releasably locks into the storage element.

9. An implant syringe as claimed in claim 1, wherein the storage element consists of a transparent plastic material.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0014] FIG. 1 is a plan view, a side view and a sectional view of a cannula unit;

[0015] FIG. 2 is a side view, a perspective view and a partly cutaway view of a protective cap;

[0016] FIG. 3 is a plan view, a side view and a sectional view of the cannula element with a protective cap in the assembled state;

[0017] FIG. 4 is a side view and a sectional view of an applicator for fitting with a filled cannula unit; and

[0018] FIG. 5 is an enlarged sectional view of a region of a conical receiving member with an inserted cannula unit.

DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS

[0019] FIG. 1 shows, in a number of views, a cannula 1, which is overmoulded with a storage element 2. The storage element 2 includes a central passage 3, which is in alignment with the passage 4 in the cannula 1. The rear edge 5 of the cannula is covered by the moulded on storage element 2 so that a solid material implant 6 inserted into the passage 3 in the storage element 2 may be slid smoothly into the passage 4 in the cannula 1.

[0020] Projecting into the passage 3 is a spring arm 7, which is cut free from the peripheral wall of the storage element 2 and which, in the unloaded state, so narrows the passage 3 that a solid material implant received therein can be jammed therein by the spring arm 7. The spring arm 7 has a gently convex shape extending into the passage 3 and is constructed integrally with the remainder of the storage element 2. When the solid material implant 6 is advanced by a piston, it presses the solid material implant smoothly through the narrow section, whereby the spring arm is forced somewhat outwardly. The jamming diameter for the solid material implant 6 can be adjusted by the height of the projection nose 8 on the spring arm 7.

[0021] FIG. 2 shows different views of a protective cap 9, which is placed on the storage element 2, before it is inserted into the applicator 10. The protective cap 9 has reinforcing ribs 11, which extend in the longitudinal direction and of which one rib 12 is flattened for positional orientation in automatic assembly. The closed front wall 13 additionally includes a recess 14 for positionally orientated, automated assembly.

[0022] FIG. 3 shows, in different views, the protective cap 9 when positioned on the storage element 2. It may be seen in the enlarged view of FIG. 5 that the protective cap 9 locks into an annular groove 16 in the storage element 2 with radially inner, pimple-shaped projections 15, whereby the locking connection is readily releasable.

[0023] A hook-shaped projection 17 may be seen in FIGS. 1 and 3, with which the storage element 2 is to be unreleasably locked in the applicator 10. FIG. 5 shows, in a greatly enlarged view, that the outer sleeve 18 of the applicator 10 has radially inwardly projecting webs 19, which are integrally connected to an annular receiving member 20. The annular receiving member 20 tapers conically in the insertion direction (arrow 21). The webs 19 engage through slots, extending in the direction of the arrow 21, in an inner sleeve 22, on which the outer sleeve 18 is slidably located.

[0024] The cannula unit consisting of the cannula 1 and storage element 2 is slid into the conical receiving member 20, whereby the hook-shaped projection 17 on the storage element 2 elastically widens the annular receiving member 20 and snaps behind the rear end edge of the receiving member 20. The insertion is limited by an annular projection 23 on the storage element 20, which, together with the rear edge of the protective cap 9, engages the radial webs 19.

[0025] FIG. 4 shows that projecting into the passage 3 of the storage element 2 there is a rear piston 24, by which the solid material implant 6 can be advanced to the tip of the cannula 1. When the outer sleeve 17 is released by a hook-shaped projection 25, it is retracted together with the cannula unit until the cannula 1 is situated within the inner sleeve 22, whereby the solid material implant 6 remains in the body of a patient.