Abstract: Devices for the occlusion of body cavities, such as the embolization of vascular aneurysms and the like, and methods for making and using such devices. The devices may include novel expansile materials, novel infrastructure design, or both. The devices provided are very flexible and enable deployment with reduced or no damage to bodily tissues, conduits, cavities, or similar structures.

Abstract: There are disclosed various dispensing mechanisms for dispensing filamentary material (24) through a catheter (12) into a treatment site of a patient, for example into an aneurysm sack (20) in a patient's vessel (22). In one embodiment the assembly (100) includes a conical material carrier (150) which is substantially aligned with the dispensing direction, thereby avoiding the need to have a rotating carrier. Another embodiment has a carrier (340) which is at least partially cylindrical. The carrier (150, 340) provides for efficient dispensation of filamentary material at substantial dispensing speeds.

Abstract: One aspect of the present invention relates to a tissue resection guide that includes a central body, a first flange and a second flange, the flanges having first and second guide surfaces, respectively, suitable for use in tissue resection. Each guide surface lies on a cutting plane, both planes intersecting interior to the flanges. In the embodiments described, the availability of two cutting planes ensures resections in more than one plane are possible. As a result, bone segments can be removed via a cut on two planes without the need to cut across an entire section of bone on one plane. In some embodiments, an opening exists between the first flange and the second flange to ensure that each resection overlaps. In other aspects of the invention, systems and methods of use for the tissue resection guide are described.

Abstract: A system includes a guide arm, a ratchet arm frame configured to be coupled to the guide arm, a ratchet arm configured to be coupled to the ratchet arm frame, and a sagittal sizing guide body configured to be coupled to the ratchet arm. The sagittal sizing guide body includes a first radiopaque object disposed at a first position and a second radiopaque object disposed at a second position that is spaced apart from the first position. The first radiopaque object has a length that corresponds to a length of a second prosthesis component. When the surgical alignment system is positioned for use on a patient, the first radiopaque object identifies a location at which a first resection of a first bone is to be performed. The second radiopaque object has a profile that corresponds to a profile of a first prosthesis component for installation on a second bone.

Abstract: A customized unicompartmental tibial cutting guide for orthopedic surgery is provided. The tibial cutting guide includes a first mating surface having a customized patient-specific negative contour to match a corresponding contour of an anterior region of a tibia of a patient and a second mating surface extending transverse to the first mating surface to a midpoint of a tibial plateau of a medial or lateral condyle of the tibia. The second mating surface includes a customized patient-specific negative contour to match a corresponding contour of a mid-region of the tibial plateau of the medial or lateral condyle. The second mating surface is limited to a region between an intercondyloid eminence and a lateral or medial edge of the tibial plateau. The tibial cutting guide also includes a first cutting guide surface and a second cutting guide surface positioned transverse to the first cutting guide surface.

Abstract: A clot removal device has a segment that has two main struts that serve as a frame for holding a plurality of secondary struts. Each of the two main struts has a proximal end that is connected at a proximal point of the segment and extends along a generally circumferential path, with each main strut terminating at a separate connecting point that is distal from the proximal point. The connecting points are connected to each other to form a generally tubular structure defining an inner lumen. The plurality of secondary struts forms a lattice of cells, with each cell surrounded by four secondary struts. Two generally straight distal struts are connected to the lattice of cells at a distal end of the segment, and are connected to each other to form a distal point. A distal opening is defined by the cells adjacent the distal struts, the distal opening communicating with the lumen and terminating at the proximal point.

Abstract: A handle for use with a surgical instrument system can comprise a first handle housing portion comprising an output and a second handle housing portion comprising, one, an electric motor comprising a rotatable motor shaft and, two, an actuator for operating the electric motor. The handle further comprises an articulation joint, wherein the second handle housing portion is rotatably connected to the first handle housing portion about the articulation joint, and wherein the second handle housing portion is rotatable between a first grip position and a second grip position. The handle further includes a transmission configured to transmit motion between the first motor shaft and the output. In various instances, the transmission comprises a cable and a slip joint configured to adjust the length of the cable depending on the position of said second handle housing portion.

Abstract: Systems, devices and methods to access and/or treat targeted body tissue (e.g., tendon tissue, ligament tissue, muscle tissue, bony tissue, and the like) under the guidance of ultrasound imaging equipment are described. Such systems can permit the intra-operative identification of the targeted tissue and the ability to deliver the appropriate instrumentation to that tissue.

Abstract: An apparatus comprises a body, a shaft assembly, an end effector, and a shield member. The shaft assembly extends distally from the body. The end effector is located at a distal end of the shaft assembly. The end effector comprises an ultrasonic blade and a clamp arm. The ultrasonic blade is configured to vibrate at an ultrasonic frequency. The clamp arm is movable toward the ultrasonic blade to compress tissue against the ultrasonic blade. The shield member is selectively movable from a first position to a second position in response to movement of the clamp arm toward the ultrasonic blade. The shield member is configured cover at least a first portion of the ultrasonic blade in the first position. The shield member is configured to uncover the first portion of the ultrasonic blade in the second position.

Abstract: Skin graft harvesting systems and methods are disclosed that utilize sensors to automate the harvesting of skin grafts or assist a user in deciding when the skin graft is ready to be harvested. Such systems and methods can reduce the burden of visual observation and ensure greater reliability and consistency of the grafts. The invention is particularly useful with harvesters that rely upon suction and/or heating to raise a plurality of small or “micro” blisters simultaneously.

Abstract: A skin graft mesher including a cutting roller and a guide roller rotatably mounted to a fixture. A skin graft may be advanced through the mesher between the rollers to form a pattern of perforations in the skin graft. The cutting roller includes cutting rings disposed on an axle and rotatable therewith. The cutting roller further includes a tissue clearing structure positioned between adjacent cutting rings with the axle extending through the tissue clearing structure and rotatable relative to the tissue clearing structure. The tissue clearing structure may clear tissue from between adjacent cutting rings during operation of the skin graft mesher. The tissue clearing structure may be eccentrically rotated about the axle between adjacent cutting rings with the tissue clearing structure extending radially outward beyond the outer diameter of the cutting ring around less than the entire outer circumference of the cutting ring.

Abstract: A puncture assistance device for use in connection with an ultrasound probe to guide a Veress needle through the layers of the wall into a bodily cavity is provided. The puncture assistance device comprises a tenaculum-like forceps, a needle guide body provided with a slot for guiding the Veress needle within the scan plane of the ultrasound probe, attachment means to the ultrasound probe, and attachment means of the needle guide to the tenaculum-like forceps. Also provided is a balloon catheter for use as a retractor in gaining access into the abdominal cavity, presenting at its distal end an inflatable balloon membrane and an framework of non-distendable flexible fibers disposed in a specific arrangement. A method access the abdominal cavity with the aid of said devices under ultrasound guidance is also provided.

Abstract: A surgical trocar 10 has an elongate shaft 12 with a leading point or edge 28 for piercing flesh and a thumb grip region 22 at an inner bend region 18. The grip region may include a flat zone and can be integral with the shaft, optionally stamped or pressed into the material of the shaft.

Abstract: A percuscopic access device is disclosed. The percuscopic access device has a hollow shaft with a proximal opening and a distal opening. The percuscopic access device also has one or more barrier ridges on the outside of the hollow shaft. The percuscopic access device also has one or more recesses on the inside of the hollow shaft and in communication with the distal opening. A cleaning obturator for use with the percuscopic access device is also disclosed. The cleaning obturator and percuscopic access device may be combined as a surgical apparatus. The cleaning obturator has a guide rod having a proximal end and a distal end. The cleaning obturator also has a plugging tip on the distal end. The cleaning obturator further has one or more swab guides proximal to the plugging tip.

Abstract: An endoluminal needle or punch is describes wherein the distal end of the endoluminal needle is able to articulate laterally out of the longitudinal axis of the steerable endoluminal needle. The endoluminal needle further comprise a blunted distal end configuration that is minimally traumatic. Under control by the user, at the proximal end of the endoluminal needle, a sharp stylet can be advanced to punch tissue and then be retracted to maximize safety. The endoluminal needle is configured for use within an introducer.

Abstract: An orthopedic device includes a fixator body having a first part and a second part that are connected by a joint and having an internally threaded bore extending longitudinally therethrough. A first pair of opposed longitudinally extending slots is provided in the first part and a second pair of opposed longitudinally extending slots is provided in the second part. A first and second pin-holders are received within and threadably engage the internally threaded bore of the first part and the second part, respectively, and are configured to removably hold a first and second sets of one or more bone fixation pins extending through the first and second pairs of opposed longitudinally extending slots, respectively.

Abstract: A pedicle insulator implant is designed to protect the nerves and surrounding tissue from injury by pedicle screws or other surgical devices and instruments. In its basic structure, the implant has a thicker section and a thinner section, the thicker section providing protection for nerves and other sensitive tissues while the thinner section can be deformable and provides grip. In one variation of the basic structure, the thinner section possess a rough surface when it is desirable in situations to provide further grip of the assembly and prevent rotation during the insertion of, for example, a pedicle screw.

Abstract: Orthopedic fixation devices and methods of installing the same. The orthopedic fixation device may include a coupling element and a bone fastener, whereby the bone fastener can be loaded into the coupling element through the bottom of a bore in the coupling element.

Abstract: A bone fastener includes a first portion that defines a longitudinal axis and includes an inner surface defining an implant cavity. A second portion that includes a first end and a second end configured to penetrate tissue. A retainer includes a wall having a first end surface and a second end surface. The wall including at least one first elongated cavity and at least one second elongated cavity. The first cavity includes a gap of the first end surface and the second cavity including a gap of the second end surface. The wall further includes an inner surface disposed about the first end. Systems and methods are disclosed.

Abstract: The present disclosure relates, according to some embodiments, to orthopedic implantable device technology, and more specifically to implantable devices for use in stabilizing the occipitocervical junction and the cervical spine. For example, the disclosure relates to embodiments of an implantable orthopedic assembly generally comprising an occipital plate and one or more repositionable clamping assemblies for securing a stabilizing rod at a nonzero distance from a plate surface. One or more rails may extend laterally from a plate to support a clamping assemblies.

Abstract: Among other things, there are disclosed embodiments of an intramedullary nail system for use in pediatric cases, including an intramedullary nail and a targeting assembly. Embodiments of the nail may be one-piece and include a proximal portion, a medial portion and a distal portion. The junction of the medial portion and distal portion is a bend that provides a small angle between the medial portion and the distal portion as viewed when the nail is substantially in a medial-lateral plane. The targeting assembly attaches to the proximal portion of the nail securely and enables easy insertion of fixing screws.

Abstract: A plate for attaching to an anatomic structure. The plate comprises a top surface opposite a bottom surface. An opening through the top and bottom surfaces is configured to receive a fastener to attach the plate to the anatomic structure. The plate comprises spikes configured to penetrate the anatomic structure. With the fastener, the spikes prevent rotational movement of the body relative to the anatomic structure. The bottom surface is concave between the spikes and defines a space configured to accommodate portions of the anatomic structure. Bone pad surfaces are configured to prevent further penetration of the spikes into the anatomic structure when in contact the same. A tracking device for a surgical navigational system can comprise a tracking head coupled to the plate with a mounting arm. The plate, when attached to the anatomic structure, prevents movement of the tracking device relative to the anatomic structure.

Abstract: A bone fixing system useful for holding bone in position, and a method for installing the same are disclosed. The ends of a conformable ligature are passed around bones, bone grafts, tendons, plates, rods, fasteners, or other anatomical or implanted structures, and the like to form a loop extending from a first portion of a body. The ends of the conformable ligature are passed through the body and extend out a second portion of the body. The ends may be attached to a tensioning tool and a selected tension may be applied. A closure member may engage an engagement portion of the body to create a friction force to hold the conformable ligature in place without significant movement relative to the body.

Abstract: The invention relates to a surgical locking screw for fastening bone parts in the event of a heel fracture, comprising a front end, a rear driving end having a drive for turning the locking screw, and an external thread, which has a constant thread pitch continuously over the axial extent of the external thread, wherein a major diameter of the external thread is constant in a first axial segment of the locking screw and increases with increasing distance from the front end in a second axial segment adjacent to the first axial segment in the direction of the rear end, wherein a minor diameter of the external thread is constant in the first and second axial segments, wherein the external thread extends, at least approximately, axially continuously over the entire axial extent of the locking screw, and wherein the minor diameter of the external thread extends over the entire axial extent of the external thread.

Abstract: The invention features improved bone screws, a delivery manifold for delivering a flowable medium to a bone screw, and washers for use with the bone screw to provide compressive fixation. The invention also features methods of treatment using the bone screws, washers, and/or delivery manifold, and kits that include the same.

Abstract: Apparatus and methods for securing a bone implant are provided. The implant may be an expandable implant. The implant may be a non-expandable implant. The implant may be for repairing a bone fracture. The implant may be secured to a bone by anchors. The implant may include anchor receiving features. The anchor receiving features may be configured to direct an anchor into cortical bone. The anchor receiving features may be configured to receive an anchor driven through cortical bone. The implant may include bone engaging members configured to engage cancellous bone. An implant may include different profiles. The different profiles may be configured to secure the implant. The profiles may be configured to support the bone. The implant may have different flexing properties configured to position the implant in the bone. The implant may be positioned to receive an anchor driven through an outside of the bone.

Abstract: A method of treating abnormal tissue within a patient includes positioning a delivery cannula within the patient, the delivery cannula having a first electrode disposed on its distal end; introducing an ablation probe through the cannula and out an open distal end thereof, so that a second ablation electrode carried on the ablation probe contacts abnormal tissue within the patient; conveying ablation energy between the first and second ablation electrodes to ablate the abnormal tissue; and introducing a separate medical element, whether a device or a therapeutic agent, through the cannula before or after the ablation process.

Abstract: A cryoablation method, system, and device that allows for real-time and accurate assessment and monitoring of PV occlusion and lesion formation without the need for expensive imaging systems and without patient exposure to radiation. The system includes a cryoballoon catheter with a cryoballoon, a distal electrode, a proximal electrode, and a temperature sensor. Impedance measurements recorded by the electrodes may be used to predict ice formation, quality of pulmonary vein occlusion, and lesion formation.

Abstract: A system and method of using a source of low-pressure refrigerant for a cryotherapy procedure. The system may generally include a fluid reservoir and a fluid flow path in thermal exchange with the fluid reservoir, the fluid flow path including a thermal exchange device in thermal exchange with the fluid reservoir, a compressor in fluid communication with the thermal exchange device, a condenser, a reversing valve located between the compressor and the condenser, and an expansion valve located between the condenser and the thermal exchange device. The method may include transferring a low-pressure refrigerant to a first fluid reservoir, reducing the temperature of the refrigerant within the first fluid reservoir, increasing the temperature of the refrigerant within the first fluid reservoir, and transferring the pressurized refrigerant from the first fluid reservoir to a second fluid reservoir.

Abstract: Devices and methods for ablating tissue in the wall of various organs of the gastrointestinal tract of a patient in order to cure or ameliorate metabolic pathophysiological conditions such as obesity, insulin resistance, or type 2 diabetes mellitus are provided. Ablational treatment of target areas may be fractional or partial, rendering a post-treatment portion of target tissue ablated and another portion that is substantially intact. Fractional ablation is achieved by controlling the delivery of ablational energy across the surface area being treated, and controlling the depth of energy penetration into tissue. Surface area control of energy delivery may controlled by the spatial pattern of distributed ablation elements or by the selective activation of a subset of a dense pattern of ablation elements. Embodiments of the device include an ablational electrode array that spans 360 degrees and an array that spans an arc of less than 360 degrees.

Abstract: A plasma generating device that utilizes a cold plasma to contain and direct a stream of electrons with a hand held nozzle to enhance healing of wounds and skin surface abnormalities, and to kill pathogens on skin surfaces in humans and animals wounds, abnormalities and pathogens.

Abstract: In accordance with at least one aspect of this disclosure, an ablation apparatus includes a proximal body portion, a shaft extending distally from the proximal body portion, the shaft being selectively deformable utilizing at least one deformation system between a first position wherein the shaft is straight an a second position wherein the shaft is bent, the at least one deformation system configured to retain the shaft in each of the first and second positions, and at least one electrode disposed at least partially within the shaft, the electrode movable with the shaft upon movement of the shaft between the first and second positions.

Abstract: An apparatus for operating on tissue comprises an end effector disposed at the distal end of an elongate shaft and including a first jaw and a second jaw that is selectively pivotable toward and away from the first jaw to capture tissue. A trigger is configured to move the second jaw toward and away from the first jaw. The locking mechanism in the locked state is configured to allow movement of the second jaw along a first path where a relative angle between the first jaw and the second jaw is limited to a first maximum angle. The locking mechanism in the unlocked state is configured to allow movement of the second jaw along a second path where the relative angle between the first jaw and the second jaw is limited to a second maximum angle. The second maximum angle is greater than the first maximum angle.

Abstract: Body tissue ablation is carried out by inserting a probe into a body of a living subject, urging the probe into contact with a tissue in the body, generating energy at a power output level, and transmitting the generated energy into the tissue via the probe. While transmitting the generated energy the ablation is further carried out by determining a measured temperature of the tissue and a measured power level of the transmitted energy, and controlling the power output level responsively to a function of the measured temperature and the measured power level. Related apparatus for carrying out the ablation is also described.

Abstract: A high-frequency surgical device for treating a tissue surface, device having an electrode device, in which a first electrode is formed on a working surface intended for contact with the tissue, and having a high-frequency generator, to the one pole of which the first electrode can be connected for operation. The surgical device is wherein a second electrode is formed on the working surface which electrode can be connected to the same pole, wherein a control device is connected to this and is designed initially to connect the first electrode and then to switch on the second electrode.

Abstract: An electrosurgical device is provided and includes a handset having a shaft extending therefrom. The electrosurgical device includes a pair of electrodes disposed at a distal end of the shaft. One or more sensors are in operable communication with the pair of electrodes to detect a pressure applied thereto. The amount of electrosurgical energy that is transmitted to the pair of electrodes is proportional to the amount of pressure that is applied to the pair of electrodes and detected by the sensor.

Abstract: A forceps includes first and second shaft members, each having a jaw member disposed at a distal end thereof. The first and second shaft members are pivotably coupled to one another toward the distal ends thereof and are moveable relative to one another between an open position and a closed position for moving the jaw members between a spaced-apart position and an approximated position. A knife assembly including a handle and a knife extending from the handle is also provided. The knife assembly is selectively translatable between a retracted position and an extended position, wherein the knife extends between the jaw members. The handle is disposed between the first and second shaft members and is configured to block further closure of the first and second shaft members beyond the closed position, thereby defining a minimum gap distance between the jaw members.

Abstract: A treatment device configured to hold a living tissue includes a swing member supported by a first grasping member and rotatable in a first direction and in an opposite direction opposite to the first direction. A support shaft of the swing member is supported on a side close to the distal end including a middle position between the distal end and the proximal end. A first holding surface is provided on the swing member close to a side of the second grasping member and grasps the living tissue. A second holding surface is provided on the second grasping member close to a side of the swing member and which faces the first holding surface and which is configured to hold the living tissue together with the first holding surface of the swing member.

Abstract: A method and system of providing therapy to a patient's uterus is provided, which can include any number of features. The method can include the steps of inserting a uterine device into the uterus and performing a uterine integrity test to determine that the uterus is intact and not perforated. If it is determined that the uterus is not perforated, a patency test can be performed to determine that the uterine device is not clogged or embedded in tissue. If the uterus is intact and the device is not clogged or embedded in tissue, the uterus can be treated with the uterine device, e.g., uterine ablation. Systems for performing these methods are also disclosed.

Abstract: A radio frequency ablation device, comprising a radio frequency ablation tube (10), a control handle (20) and a temperature-controlling radio frequency instrument (35). The middle section of the radio frequency ablation tube (10) carries a strip-shaped connecting electrode; a radio frequency electrode (12) is formed at the distal end of the radio frequency ablation tube (10) and connected to the control handle (20) via the strip-shaped connecting electrode. The control handle (20) comprises a control guiding control a tube electrode control handle (23) and a tube electrode auxiliary control handle (24) An integrated interface (50) is disposed at the rear of the control handle (20), and the temperature-controlling radio frequency instrument (35) is connected to the integrated interface (50) via an integrated cable (34). And a radio frequency electrode (12) a radio frequency ablation tube (10) and a guide tube (16) are also provided.

Abstract: An apparatus includes a balloon adapted to be placed adjacent a calcified region of a body. The balloon is inflatable with a liquid. The apparatus further includes a shock wave generator within the balloon that produces shock waves that propagate through the liquid for impinging upon the calcified region adjacent the balloon. The shock wave generator includes a plurality of shock wave sources distributed within the balloon.

Abstract: Devices and methods are disclosed for treating tissue with microwave energy. Such devices and methods are able to treat cavities or surface tissue by creating one or more area or volumetric lesions. Also disclosed are flexible, low-profile devices that can be inserted non-invasively or minimally invasively near or into the target tissue as well as microwave antennas designed to generate ablation profiles that can ablate a large area or a large volume of target tissue in a single ablation. The devices include antennas wherein the field profile generated by an antenna is tailored and optimized for a particular clinical application. The antennas use unique properties of microwaves such as interaction of a microwave field with a metallic object and the use of additional shaping elements to shape the microwave field.

Abstract: A microwave applicator for insertion into living body tissue for use in microwave coagulation and ablation treatments includes a microwave transmission line extending between an attachment end of the applicator and an antenna toward an insertion end of the applicator with an outer conductive sleeve forming an enclosed fluid space around the transmission line. A fluid circulation system circulates fluid in the fluid space. A portion of or all of the circulating fluid can be injected into tissue that surrounds the applicator body from approximately the proximal end of a desired heating zone produced by microwave energy radiated from the antenna along the applicator body toward the proximal end of the applicator to hydrate and wet the tissue outside the proximal end of the desired heating zone to reduce the drying of this tissue and limit extension of the heating and ablation zone proximally along the applicator body.

Abstract: A method for treating tissue through a branched luminal network of a patient is provided. A pathway to a point of interest in branched luminal network of a patient is generated. An extended working channel is advanced transorally into the branched luminal network and along the pathway to the point of interest. The extended working channel may be positioned in a substantially fixed orientation at the point interest. A tool is advanced though the extended working channel to the point of interest. Tissue at the point of interest is treated.

Abstract: A microwave ablation catheter is provided. The microwave ablation catheter includes a coaxial cable connected at its proximal end to a microwave energy source and at its distal end to a distal radiating section. The coaxial cable includes inner and outer conductors and a dielectric positioned therebetween. The inner conductor extends distally past the outer conductor and is in sealed engagement with the distal radiating section. A balun is formed in part from a conductive material electrically connected to the outer conductor of the coaxial cable and extends along at least a portion of the coaxial cable. The conductive material has a braided configuration and is covered by at least one insulative material.

Abstract: The present disclosure provides, according to some embodiments, methods and systems for selectively reducing, blocking or inhibiting at least part of the neural activity in an organ of a subject. In preferred embodiments, the method and system are used for selectively blocking at least part of the neural activity in a duodenum of a subject in need thereof. According to some embodiments, the selective blocking occurs through use of laser radiation. According to some embodiments, the selective blocking comprises causing damage to at least part of sensory nerves located within a target area while maintaining functional activity of tissue surrounding the sensory nerves. According to some embodiments, the sensory nerves include neurons configured to transmit signals triggered by food passing through the duodenum, such as, but not limited to, neurohormonal signals.

Abstract: The present invention provides a method of fixating a mesh implant to a tissue of a subject comprising attaching said mesh implant to said tissue, covering said mesh implant by an antiadhesive barrier, wherein said antiadhesive barrier is attached to said mesh implant by a biocompatible adhesive.

Abstract: Apparatus and systems herein support sharps containers and medical instruments trays, brackets, fasteners or holders on a mayo cart. Embodiments include an apparatus for attaching to a mayo cart to support a detachably mounted container, bracket or holder. A first portion has an arm extended to approximately the distance from the mayo cart vertical support pole to an outer edge of a mayo cart tray. A second portion attaches to the vertical pole proximate one end of the apparatus. A third portion attaches with the detachable container, bracket or holder proximate the opposite end of the apparatus. Embodiments may also include a detachable container, bracket or holder comprising an attachment portion to receive the third portion of the support apparatus for supportively attaching to the mayo cart. The support apparatus arm may also be extended to an adjustable length for attaching the container, bracket or holder with the mayo cart.

Abstract: The invention provides an easy-to-manipulate manipulator comprising a manipulating part, a manual joint part that is driven directly by displacement of the manipulating part, a detection unit for detecting an amount of displacement of the manipulating part, a device that moves depending on the amount of displacement detected at the detection unit, an electric joint part that is driven by the device, and a selection portion for selectively determining whether the electric joint part is driven or not.

Abstract: 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.