An endoscopic instrument having an instrument body configured in a long, slim and flexible manner. The instrument may be completely or partly wound in one or more windings that allows the instrument to be packed in a space-saving and easy-to-handle manner. To keep the instrument body in this position, a holding device is provided that is arranged on the instrument body and is preferably undetachably held there. The holding device has a gripper rotatably supported around the instrument body. The instrument body has a latch to hold and fasten the windings.

A treatment tool device for an endoscope includes a treatment tool main body and an oversheath. The treatment tool main body includes a flexible sheath, an operation wire, a snare wire, and a hard part. The operation wire is inserted through the flexible sheath. The hard part is provided at a base end portion of the flexible sheath. The oversheath is inserted into a forceps channel in a state where the flexible sheath and the hard part are inserted into the oversheath.

An imaging coupler comprises an elongate device connector configured to couple to an elongate device. The imaging coupler further comprises an instrument connector configured to couple to an imaging instrument. The imaging instrument is configured to be slidably received within a lumen of the elongate device. The imaging coupler further comprises a body portion extending between the elongate device connector and the instrument connector. The imaging coupler further comprises a tubular member coupled to the instrument connector and extending within the body portion. The instrument connector is movable in parallel with a longitudinal axis of the tubular member while the elongate device is coupled to the elongate device connector.

An endoscope includes a distal tip with a sterile cap disposed on the distal tip. The sterile cap reduces the exposure of the distal tip to contamination and includes an integrating sphere that enables calibration of an image sensor disposed in the endoscope. By enabling calibration of the image sensor while the sterile cap remains on the distal tip of the endoscope, the image sensor can be calibrated while maintaining the sterility of the endoscope. The sterile cap can be disposed on the distal tip of the endoscope under sterile conditions, placed in a sterile packaging, and can be removed just before a medical procedure to reduce the risk of exposing the endoscope to contamination.

A medical visualisation system including a first medical visualisation device having a first device colour identifier, a second medical visualisation device having a second device colour identifier, a third medical visualisation device having a third device colour identifier, and a monitor device, the first device colour identifier being a first colour, the second device colour identifier being a second colour, and the third device colour identifier being a third colour. The first colour has a first hue angle, the second colour has a second hue angle, and the third colour has a third hue angle, wherein the first hue angle and the second hue angle differ by more than 40 degrees, the second hue angle and the third hue angle differ by more than 40 degrees, and the third hue angle and the first hue angle differ by more than 40 degrees.

A multifunctional enclosure is described having an elongated sleeve configured with an enlarged opening for the insertion of an elongated member of a medical probe. The multifunctional enclosure is configured to prevent the elongated member of the medical probe from swinging and becoming damaged during transport. The multifunctional enclosure may further comprise an attachment component for securing the medical probe to the multifunctional enclosure. Furthermore, at least one vent may be configured onto the multifunctional enclosure, such as on a first end closure portion. The vent may allow for adequate flow for sterilization and/or drying.

A disposable handle assembly may include a housing including an end wall at a distal end of the housing and first extension walls extending from the end wall, an end cap attached to a second extension wall on a proximal end of the housing, and a power source positioned within the housing between the distal end and the end cap. The disposable handle assembly may include a pin positioned within the housing, a circuit wire positioned within the housing, and a plate attachment positioned on the end wall between the first extension walls. The circuit wire may be in electrical contact with the contact plate and an end of the power source received by the end cap. The pin and the contact plate may be electrically connected outside of the housing and close an electrical circuit of the disposable handle assembly.

A method for conditioning a flexible medical endoscope (10) having internal channels (12), so as to maintain disinfection of said endoscope (10) following processing to a state of high level disinfection, comprises the steps of: (a) connecting the internal channels (12) of the endoscope (10) to connectors (31-34) enabling fluid communication with a reservoir (24) of disinfectant fluid (25); (b) charging the internal channels (12) with disinfectant fluid (25) from the reservoir (24); (c) disconnecting the internal channels (12) from the connectors (31-34); (d) sealing the endoscope (10) in a pouch (56) having a substantially air-tight seal (57) and a valve (55) enabling connection to suction means (53); and (e) connecting and activating the suction means (53) so as substantially to reduce pressure within the pouch (56), thereby partially evacuating the pouch (56).

The present disclosure relates to a cap for protecting an imaging instrument from damage caused by impact or poor handling. Exemplary devices can include a rigid outer shell and soft inner lining surrounding a distal tip of the instrument, to be applied between instrument use, and during instrument transport, disinfection, sterilization, and storage.

An endoscope apparatus provided in the invention has forced disposability of a cannula by the means and techniques put in place so that the parts in contact with organic tissues or the detection of container extraction cannot be used, re-used, or if re-used, in a way that aligns with their operating limits. Activation of the cannula is detected and traced using sensors or wireless intercommunication devices so that when a certain time lapses or a certain number of activations after the first activation of the cannula, a limited usage means disables the cannula in mechanical or electrical way to ensure forced disposability of the cannula.