An end effector for use with a surgical stapling instrument is disclosed. The end effector comprises a first jaw, a second jaw movable relative to the first jaw to grasp tissue therebetween, and a staple cartridge. The staple cartridge comprises staples deployable into the tissue. The end effector further comprises a magnetic sensor configured to measure a parameter indicative of an identifying characteristic of the staple cartridge, an impedance sensor configured to measure a parameter indicative of an impedance of the tissue, and a processing unit in communication with the impedance sensor. The processing unit is configured to determine a property of the tissue based on an output of the impedance sensor.

A surgical stapling system including a shaft assembly transmits actuation motions from an actuator and an end effector compresses and staples tissue. The end effector comprises a channel; an anvil having a staple forming surface is moveable relative to the channel between open and closed positions; the anvil having a magnet at a distal end; and a staple cartridge removably positionable within the channel. The staple cartridge comprises a body supported for a confronting relationship with the anvil in its closed position; a plurality of staple drivers located within the cartridge body support a staple; a Hall effect sensor located at the distal end of the body; and a microprocessor in communication with the Hall effect sensor. The Hall effect sensor and the microprocessor receive power when the staple cartridge is positioned within the channel, and the system is operable to identify a staple cartridge.

A sanitary monitoring system, the system including: one or more conduits configured to be connected to a medical device; one or more measurement devices configured to assist in determining one or more flow rates associated with the medical device from a fluid flow provided through the one or more conduits; and a status device configured to determine a sanitary condition of the medical device from the one or more flow rates.

A method for monitoring a reprocessing device for endoscopes the method including: logging one or more process parameters as well as a time of each reprocessing operation over a plurality of reprocessing operations for at least one endoscope in at least one reprocessing device; storing the logged one or more process parameters in association with the respective reprocessing operation, and performing a trend analysis of at least one logged process parameter in an evaluation device via the one or more logged process parameters.

Provided among other things is a sampling system for determining an amount or type of contamination a narrow, elongated passageway in a medical device, said sampling system comprising: (a) a fluid supply system that supplies to said passageway a sampling liquid for flowing through said passageway and a gas for flowing through said passageway; and (b) a receiving container that receives liquid from said passageway, wherein said sampling liquid is sterile, wherein said sampling liquid is configured to allow recovery of viable pathogens from the passageway, and wherein said sampling liquid comprises an amount and selection of surfactant effective to enhance the dislodgement of Enterococcus faecalis and Pseudomonas aeruginosa bacteria from the narrow passageways.

A cleaning indicator including a substrate having an image upon it that can be interrogated to assist in monitoring a process for washing articles in a washing machine system. The image can be a printed image, which in turn is covered at least partially by a test soil to be removed by the washing process. Alternatively, the test soil can be formed into an image on the substrate. The cleaning indicator can be imaged before the start of a washing process to allow the washing process to proceed only if the appropriate image is observed. The cleaning indicator can be imaged during operation of the washing process, and when a criterion for cleanliness is met, the washing process can be automatically terminated. A washing system for using the cleaning indicator in an automated washing process is also disclosed.

A surgical instrument flow indicator comprises a body defining a flow passage comprising an inlet and an outlet, wherein the inlet is configured to be fluidically coupled to a fluid supply source and wherein the outlet is configured to be fluidically coupled to the surgical instrument. The flow indicator further comprises a flow indication mechanism in flow communication with the flow passage, the flow indication mechanism being configured to transition from a first state to a second state in response to a threshold force exerted on the flow indication mechanism, wherein in the second state, the flow indication mechanism has an arrangement indicating to an observer that the flow indication mechanism transitioned from the first state to the second state.

A method of assessing the efficiency of a cleaning operation and assessing likely residual contamination on substrates after a cleaning operation.

Described are a method, system, and computer program product for guided and tracked cleaning of medical devices. The method includes determining an item identifier of an item to be cleaned and determining cleaning instructions based on the item identifier. The cleaning instructions include a plurality of steps defining cleaning actions to be performed on the item by a user. The method further includes sequentially presenting each step of the plurality of steps of the cleaning instructions. Sequentially presenting each step of the plurality of steps includes presenting the step via at least one of a visual output and an auditory output of a computing device associated with the user and determining that the step was completed based on an input received at the computing device. The method further includes updating a record associated with the item in at least one database to identify that the item was cleaned.

A device and method for testing for the presence of liquid in a cannula of a medical instrument is described. The device includes a flexible guide member having a first end, a second end and a length extending from the first end to the second end, an elongated member arranged within the flexible guide member, and an absorbent material attached to one of the elongated member. The flexible guide member is inserted into the cannula, the flexible guide member is manipulated to cause the absorbent material to move through the cannula. The absorbent material is analyzed for the presence of liquid.