A kyphoplasty system includes various instruments which can be selectively used in a surgical theater (e.g., during a surgical operation on a patient) or a surgical training environment. The kyphoplasty system can include one or more of a kyphoplasty apparatus, a prone table mat, a connector system, a bone introducer needle, and a biopsy device. The kyphoplasty system may also include a training system for use in the training environment.

Needleless connectors are described. An example needleless connector includes a housing and a compressible valve. The housing may define an internal cavity and may include a body section having a first port and one or more internal contact tabs and a base section having a valve mount and a second port. The compressible valve may be disposed within at least a portion of the internal cavity and be movably retained within the housing. The compressible valve may include a flange portion for securing the compressible valve within the housing. A central longitudinal axis of the housing may be defined by a coaxial arrangement of the first and second port. The one or more internal contact tabs may be arranged to contact an outer side surface of the flange portion such that a radial force substantially orthogonal to the central longitudinal axis is provided for securement.

Needleless connectors are described. An example needleless connector includes a housing and a compressible valve. The housing may define an internal cavity and may include a body section having a first port and one or more internal contact tabs and a base section having a valve mount and a second port. The compressible valve may be disposed within at least a portion of the internal cavity and be movably retained within the housing. The compressible valve may include a flange portion for securing the compressible valve within the housing. A central longitudinal axis of the housing may be defined by a coaxial arrangement of the first and second port. The one or more internal contact tabs may be arranged to contact an outer side surface of the flange portion such that a radial force substantially orthogonal to the central longitudinal axis is provided for securement.

A catheter enclosure device for locking an intravenous catheter therein with tamper-evident features to deter unauthorized use. The catheter enclosure device may be particularly useful for peripherally inserted central catheters (PICC). The enclosure device comprises an open-top box and a removable lid for covering the box. The open-top box has a compartment for holding the proximal end of an intravenous catheter. The lid comprises a panel for covering the open portion of the open-top box and a folding wing that overhangs the forward end of the box when covering the box. The folding wing further comprises a retaining anchor. When the folding wing is folded down, the retaining anchor inserts into a locking slot on the forward end of the box, thereby preventing the lid from being removed off the box. Also disclosed are methods for using the catheter enclosure device.

A syringe having barrel defining an outer circumferential surface, and a distal end including a non-luer tip that is not connectable to an intravenous device. The syringe barrel defines a snap-in, syringe engagement feature, adjacent to its distal end, oriented on its outer circumferential surface, which is selectively insertable within a bore of a complementary enteral collar. A proximal end of the enteral collar has a snap-in, enteral collar engagement feature, in the bore of the collar. In some embodiments, the snap-in, enteral collar engagement feature includes one or more cantilever snap joints, which engage a recess in the syringe engagement feature, upon axial insertion of the syringe tip into the bore of the collar. In some embodiments, the enteral collar engagement feature includes a discontinuous-annular snap joint. The enteral collar is sized to permit connection to an enteral device and prevent connection to a device having a luer connector.

A syringe having barrel defining an outer circumferential surface, and a distal end including a non-luer tip that is not connectable to an intravenous device. The syringe barrel defines a snap-in, syringe engagement feature, adjacent to its distal end, oriented on its outer circumferential surface, which is selectively insertable within a bore of a complementary enteral collar. A proximal end of the enteral collar has a snap-in, enteral collar engagement feature, in the bore of the collar. In some embodiments, the snap-in, enteral collar engagement feature includes one or more cantilever snap joints, which engage a recess in the syringe engagement feature, upon axial insertion of the syringe tip into the bore of the collar. In some embodiments, the enteral collar engagement feature includes a discontinuous-annular snap joint. The enteral collar is sized to permit connection to an enteral device and prevent connection to a device having a luer connector.

An integrated catheter system includes a catheter adapter including a catheter and an inlet, the catheter configured to be inserted into a patient's vasculature, a needle-free connector including a first port, a second port positioned opposite the first port, and a side port positioned between the first port and the second port, the second port including a valve member, intermediate tubing extending between the inlet of the catheter adapter and the first port of the needle-free connector, and extension tubing extending from the side port of the needle-free connector, where the needle-free connector includes chlorhexidine.

An adapter for a medical device catheter includes a proximal portion and a distal portion, at least two electrodes positioned to create an electrode gap between the electrodes, an attachment mechanism configured to secure the adapter to a distal end of a medical device catheter, and an electrical connector at the proximal portion and in electrical communication with the electrodes.

An adapter for a medical device catheter includes a proximal portion and a distal portion, at least two electrodes positioned to create an electrode gap between the electrodes, an attachment mechanism configured to secure the adapter to a distal end of a medical device catheter, and an electrical connector at the proximal portion and in electrical communication with the electrodes.

A medical fluid coupling for connecting a fluid line to a connection section of a blood treatment apparatus or for connecting to a connecting adapter comprises at least one main body. The main body includes a first latching element with a first section. The first section is designed to be elastically bendable and/or elastically tiltable. The main body may optionally include a second latching element with a second section. At least one of the first latching element and the second latching element comprises a recess for receiving a protrusion of the connection section and/or a protrusion to reach into a recess of the blood treatment apparatus or of the connecting adapter.