A reusable apparatus, such as a medical instrument or tool, is decontaminated by applying pressure waves with direct contact of the pressure wave applicator to the reusable apparatus in an open bath in a sufficient dosage to remove contamination but without adversely affecting the ability to reuse the apparatus.

A syringe assembly is provided comprising a syringe cylinder extending from an opening configured to receive a plunger to an end configured to couple with a needle and/or medical tubing, a cap configured to couple to the end, and barrier material at least partially encompassing the cap and the end. A syringe assembly is provided comprising a syringe cylinder extending from an opening configured to receive a plunger to an end configured to couple with a needle and/or medical tubing, a plunger extending from one end to a seal end, and at least one cap configured to couple to the one end. A syringe assembly is provided comprising a syringe cylinder extending from an opening configured to receive a plunger to an end configured to couple with a needle and/or medical tubing, and a plunger extending from one end to a seal end, the one end of the plunger defining a recess configured to receive at least one cap.

A syringe assembly is provided comprising a syringe cylinder extending from an opening configured to receive a plunger to an end configured to couple with a needle and/or medical tubing, a cap configured to couple to the end, and barrier material at least partially encompassing the cap and the end. A syringe assembly is provided comprising a syringe cylinder extending from an opening configured to receive a plunger to an end configured to couple with a needle and/or medical tubing, a plunger extending from one end to a seal end, and at least one cap configured to couple to the one end. A syringe assembly is provided comprising a syringe cylinder extending from an opening configured to receive a plunger to an end configured to couple with a needle and/or medical tubing, and a plunger extending from one end to a seal end, the one end of the plunger defining a recess configured to receive at least one cap.

The present invention relates to a system consisting of one or more instruments, which provides a simple method for detaching a connector cap from the connector as this is the juncture utilized to administer fluids into the body via an IV peripherally inserted central catheter, commonly know as a PICC or PIC line. This device enables one to avoid potential breakage of the PICC line connector cap, which can occur utilizing current procedures. The system is put into place whereby the portion of the instrument associated with the fixed end of the PICC line (that which is implanted in the patient) is slid over the PICC line connector and held stationary, while the portion of the accompanying instrument associated with the free end of the PICC line is secured around the connector cap and rotated counterclockwise until the connector cap assembly is loose enough to be separated without further aid.

The present invention relates to a system consisting of one or more instruments, which provides a simple method for detaching a connector cap from the connector as this is the juncture utilized to administer fluids into the body via an IV peripherally inserted central catheter, commonly know as a PICC or PIC line. This device enables one to avoid potential breakage of the PICC line connector cap, which can occur utilizing current procedures. The system is put into place whereby the portion of the instrument associated with the fixed end of the PICC line (that which is implanted in the patient) is slid over the PICC line connector and held stationary, while the portion of the accompanying instrument associated with the free end of the PICC line is secured around the connector cap and rotated counterclockwise until the connector cap assembly is loose enough to be separated without further aid.

Systems, devices and methods to improve safety and efficiency in an operating room comprise providing a suture package that holds new suture needles and needle receptacles for storing used needles. The devices can be safely worn for the surgeon to self-dispense new suture needles in the near surgical field and to secure the used needles into a needle trap or a needle retainer located on his extremity, on his operative instruments or on the surgical drapes. The device may provide automated and/or simplified needle counting both during use and after removal from the surgical field. The device may be configured for ergonomic and efficient use so as to minimize the actions and motions of the surgeon to dispense and secure the needle.

Systems, devices and methods to improve safety and efficiency in an operating room comprise providing a suture package that holds new suture needles and needle receptacles for storing used needles. The devices can be safely worn for the surgeon to self-dispense new suture needles in the near surgical field and to secure the used needles into a needle trap or a needle retainer located on his extremity, on his operative instruments or on the surgical drapes. The device may provide automated and/or simplified needle counting both during use and after removal from the surgical field. The device may be configured for ergonomic and efficient use so as to minimize the actions and motions of the surgeon to dispense and secure the needle.

A surgical device including a handle assembly, an elongated portion, at least one window, an end effector, and a shroud is disclosed. The at least one window extends through an outer wall of the elongated portion and is configured to allow fluid to travel therethrough from an interior portion of the elongated portion to ambient air. The end effector is configured to selectively engage a distal portion of the elongated portion. The shroud is affixed to the end effector and extends proximally therefrom. The shroud is configured to cover the at least one window when the end effector is engaged with the elongated portion.

A surgical device including a handle assembly, an elongated portion, at least one window, an end effector, and a shroud is disclosed. The at least one window extends through an outer wall of the elongated portion and is configured to allow fluid to travel therethrough from an interior portion of the elongated portion to ambient air. The end effector is configured to selectively engage a distal portion of the elongated portion. The shroud is affixed to the end effector and extends proximally therefrom. The shroud is configured to cover the at least one window when the end effector is engaged with the elongated portion.

A medical instrument includes an instrument shaft with exit holes near a distal end of the shaft, a tool coupled to the distal end of the shaft, and a backend. The backend may include a mechanism that manipulates a drive element that extends through the shaft and couples to the tool, a fluid inlet, and a fluid channel assembly providing fluid communication between the fluid inlet and the proximal end of the shaft. Cleaning fluid is directed into the fluid inlet, through the fluid channel assembly, and into the shaft. A chassis or other structural piece of the backend may form part of the fluid channel assembly.