A medical device processor includes a basin, a lid, and a flexible seal that seals the lid when the lid is in a sealed position and directs fluid runoff unimpeded back into the basin when the lid is the open position. The flexible seal includes a base, a flap extending from the base, and a protuberance extending from the flap. The flexible seal may be configured such that when the lid is in the sealed position at least a portion of a lower surface of the flap sealingly contacts a rim of the basin. The flexible seal may further be configured such that when the lid is in the open position, at a hinge side of the lid at least a portion of a lower surface of the protuberance has a negative slope relative to horizontal in a direction toward an opening in the basin.
A61B 1/12 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with cooling or rinsing arrangements
A medical device processor includes a basin, a lid, front and rear actuation assemblies, and a controller. The lid includes a frame and a seal window assembly removably mounted to the frame. The actuation assemblies are configured to displace the lid from a closed position to a sealed position. In the sealed position the lid compresses an elastomeric seal between the lid and the basin. The controller is configured to control pressurization of the rear actuation assemblies and to monitor a lid lift pressure of the rear actuation assemblies. As the lid moves from an open position toward the closed position, if the lid lift pressure reaches or falls below a predetermined pressure P2 prior to the closing of the lid, the controller pressurizes the rear actuation assemblies with a sufficient pressure to stop further movement of the lid or to angularly displace the lid to the open position.
3.
CHEMICAL INJECTION AND METERING MODULE FOR STERILIZATION SYSTEM
The present disclosure discusses a sterilization system having a dosing module with a dosing cylinder to allow for metered flow of a predetermined amount of sterilant fluid into the sterilization system. The dosing module can include a dosing cylinder for measuring the predetermined amount of sterilant fluid, a pump for moving the sterilant fluid, and a controller configured to initiate driving of the sterilant fluid through the dosing module and into the sterilization system. A method of providing a predetermined amount of sterilant fluid to the sterilization system can include controlling the flow of sterilant fluid into the dosing cylinder, measuring the amount of sterilant fluid in the dosing cylinder to a desired dose amount, and controlling flow of the dose into the sterilization system.
The present invention relates to the detection vapor peracetic acid and hydrogen peroxide. It finds particular application in the sensing of vapor peracetic acid and hydrogen peroxide concentrations. The system includes (a) a source of peracetic acid vapor, hydrogen peroxide vapor, water vapor and acetic acid vapor, (b) a light source which is configured to supply light with at least a component in the mid-infrared range, and (c) a detector which is configured to individually detect mid-infrared range light in (i) a first mid-infrared spectrum absorbed by the peracetic acid vapor and not absorbed by the hydrogen peroxide vapor, the acetic acid vapor or the water vapor, and (ii) a second mid-infrared spectrum absorbed by the peracetic acid vapor and the hydrogen peroxide vapor.
G01N 21/3504 - Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light for analysing gases, e.g. multi-gas analysis
G01N 21/359 - Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light using near infrared light
A medical device processor includes a chemical dosing system including a supply tube extending along a length between a first and second end. A pump is coupled to the supply tube downstream from the first end and configured to pump fluid in the tube. A bubble detector is coupled to the supply tube downstream from the first end, wherein an inner volume of the supply tube between the bubble detector and the second end is equal to or greater than a volume of a dose of liquid to be pumped from the chemical dosing system in a given dose. A controller is configured to run the pump for a predetermined period of time; detect the presence of one or more bubbles in the supply line based on measurement by the bubble detector; upon detection, continue to run the pump for the remainder of the predetermined time; and issue a notification.
A61B 1/12 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with cooling or rinsing arrangements
A61L 2/24 - Apparatus using programmed or automatic operation
A medical device processor includes a chemical dosing system including a supply tube extending along a length between a first and second end. A pump is coupled to the supply tube downstream from the first end and configured to pump fluid in the tube. A bubble detector is coupled to the supply tube downstream from the first end, wherein an inner volume of the supply tube between the bubble detector and the second end is equal to or greater than a volume of a dose of liquid to be pumped from the chemical dosing system in a given dose. A controller is configured to run the pump for a predetermined period of time; detect the presence of one or more bubbles in the supply line based on measurement by the bubble detector; upon detection, continue to run the pump for the remainder of the predetermined time; and issue a notification.
A61L 2/16 - Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using chemical substances
A61B 90/70 - Cleaning devices specially adapted for surgical instruments
A61M 1/00 - Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
B65B 57/00 - Automatic control, checking, warning or safety devices
7.
HANDLE ASSEMBLY FOR ACCESSORY OF MEDICAL DEVICE SUPPORT SYSTEM
A handle assembly for an accessory of a medical device support system. The handle assembly includes a handle, an interface device, a conductive coating, and a connector. The interface device is in an outer surface of a generally tubular section of a handle housing of the handle and is configured to receive an input or transmit an output associated with the medical device support system. The conductive coating is on the inner surface of the generally tubular section and is configured to transmit one or more of power, ground, control signals, and communication signals corresponding to the input or the output of the interface device. The connector is connected to the conductive coating and is configured to transmit the one or more of the power, ground, control signals, and communication signals from the conductive coating to another part of the accessory and/or the medical device support system.
A handle assembly for an accessory of a medical device support system. The handle assembly includes a handle, an interface device, a conductive coating, and a connector. The interface device is in an outer surface of a generally tubular section of a handle housing of the handle and is configured to receive an input or transmit an output associated with the medical device support system. The conductive coating is on the inner surface of the generally tubular section and is configured to transmit one or more of power, ground, control signals, and communication signals corresponding to the input or the output of the interface device. The connector is connected to the conductive coating and is configured to transmit the one or more of the power, ground, control signals, and communication signals from the conductive coating to another part of the accessory and/or the medical device support system.
A61B 90/30 - Devices for illuminating a surgical field, the devices having an interrelation with other surgical devices or with a surgical procedure
A61B 90/00 - Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups , e.g. for luxation treatment or for protecting wound edges
A61B 17/00 - Surgical instruments, devices or methods, e.g. tourniquets
A multi-channel selector valve includes a housing, a rotor at least partially disposed within the housing and rotatable about an axis of rotation, the rotor having a first cam surface, and a stator at least partially disposed within the housing. The housing includes a plurality of flow controllers arranged about the axis of rotation of the rotor, each flow controller including an aperture, and a blocking member disposed adjacent to the cam surface, the blocking member selectively movable relative to the aperture to open and permit flow through the aperture.
F16K 11/074 - Multiple-way valves, e.g. mixing valves; Pipe fittings incorporating such valves; Arrangement of valves and flow lines specially adapted for mixing fluid with all movable sealing faces moving as one unit comprising only sliding valves with pivoted closure members with flat sealing faces
F16K 31/04 - Operating means; Releasing devices magnetic using a motor
A surgical table includes a base, a tabletop, first and second frameworks, a cable, and a cable take-up mechanism. The first and second frameworks are moveable relative to one another to move the tabletop relative to the base in a first direction and a second direction that is opposite the first direction. The cable has a first end, a second end that is opposite the first end, and an intermediate portion. The first and second ends are mounted to the respective first and second frameworks. The cable take-up mechanism includes a constant-force spring coupled to the intermediate portion of the cable to take up slack in the cable as the first and second frameworks move relative to one another to move the tabletop relative to the base.
A surgical table includes a base, a tabletop, first and second frameworks, a cable, and a cable take-up mechanism. The first and second frameworks are moveable relative to one another to move the tabletop relative to the base in a first direction and a second direction that is opposite the first direction. The cable has a first end, a second end that is opposite the first end, and an intermediate portion. The first and second ends are mounted to the respective first and second frameworks. The cable take-up mechanism includes a constant-force spring coupled to the intermediate portion of the cable to take up slack in the cable as the first and second frameworks move relative to one another to move the tabletop relative to the base.
A multi-channel selector valve (10) includes a housing (12), a rotor (20) at least partially disposed within the housing and rotatable about an axis of rotation, the rotor having a first cam surface (26), and a stator (16) at least partially disposed within the housing. The housing includes a plurality of flow controllers (28) arranged about the axis of rotation of the rotor, each flow controller including an aperture, and a blocking member (34) disposed adjacent to the cam surface, the blocking member selectively movable relative to the aperture to open and permit flow through the aperture.
F16K 7/04 - Diaphragm cut-off apparatus, e.g. with a member deformed, but not moved bodily, to close the passage with tubular diaphragm constrictable by external radial force
F16K 31/524 - Mechanical actuating means with crank, eccentric, or cam with a cam
F16K 37/00 - Special means in or on valves or other cut-off apparatus for indicating or recording operation thereof, or for enabling an alarm to be given
13.
STERILIZABLE COVER FOR HANDLE OF ACCESSORY OF MEDICAL SUSPENDED CEILING ASSEMBLY
A sterilizable cover for a handle of an accessory of a medical suspended ceiling assembly includes a generally tubular stem portion and an annular flange portion. The generally tubular stem portion has a sufficient size to be gripped by the human hand, and has a proximal end that is open and a distal end that is closed, and defines a cavity along a longitudinal axis for receipt therein of a handle grip portion. The generally tubular stem portion includes a friction fit portion that is configured to flex radially outwardly to create a friction fit with a portion of the handle grip portion upon receipt of the handle grip portion in the cavity of the generally tubular stem portion. The annular flange portion extends radially outwardly from a proximal end of the generally tubular stem portion. The generally tubular stem portion and the annular flange portion are a single continuous piece of flexible silicone rubber.
A sterilizable cover for a handle of an accessory of a medical suspended ceiling assembly includes a generally tubular stem portion and an annular flange portion. The generally tubular stem portion has a sufficient size to be gripped by the human hand, and has a proximal end that is open and a distal end that is closed, and defines a cavity along a longitudinal axis for receipt therein of a handle grip portion. The generally tubular stem portion includes a friction fit portion that is configured to flex radially outwardly to create a friction fit with a portion of the handle grip portion upon receipt of the handle grip portion in the cavity of the generally tubular stem portion. The annular flange portion extends radially outwardly from a proximal end of the generally tubular stem portion. The generally tubular stem portion and the annular flange portion are a single continuous piece of flexible silicone rubber.
A sterilization process test device for verifying the efficacy of a sterilization process includes a tubular body defining a chamber for containing at least one sterilization indicator and a cap to sealingly close the tubular body. The tubular body includes at least one hole, which is covered by a gas and steam permeable cover. The only flow path into the chamber is provided through the steam and gas permeable cover and the at least one hole, which when combined are configured to control and restrict a flow of steam or a gaseous sterilization medium from an external environment.
A liquid sporulation method is described. A first liquid culture is prepared by adding bacterial cells to a sporulation broth, wherein an optical density (OD600) of the first liquid culture is in a range of 0.001 to 0.01. The first liquid culture is incubated and an optical density (OD600) thereof is increased to be in a range of 0.2 to 2.0. Second liquid culture is prepared by adding the incubated first liquid culture to a predetermined amount of additional sporulation broth, wherein an optical density (OD600) of the second liquid culture is in the range of 0.001 to 0.1, and a ratio of a volume of the second liquid culture to a volume of the first liquid culture is in a range of 10:1 to 150:1. The second liquid culture is incubated so an optical density (OD600) thereof is increased to be in a range of 1.0 to 4.0.
An endoscope reprocessor for reprocessing an endoscope. An actuation mechanism of the reprocessor includes an actuator housing and a plunger removably attachable to an elevator guidewire lever of the endoscope. A receiving chamber receives pressurized fluid from a pump to impart a pressurized fluid biasing force that displaces the plunger relative to the actuator housing in a first direction and a return actuator that imparts a return biasing force that displaces the plunger relative to the actuator housing in a second direction. A controller controls the pump to provide the pressurized fluid at a first pressure at which the pressurized fluid biasing force is greater than the return biasing force to displace the plunger lever in the first direction and a second pressure at which the return biasing force is greater than the pressurized fluid biasing force to displace the plunger and the lever in the second direction.
A61B 1/00 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
A61B 1/12 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with cooling or rinsing arrangements
18.
ENDOSCOPE REPROCESSOR INCLUDING ACTUATION MECHANISM FOR ACTUATING ENDOSCOPE ELEVATOR GUIDEWIRE
An endoscope reprocessor for reprocessing an endoscope. An actuation mechanism of the reprocessor includes an actuator housing and a plunger removably attachable to an elevator guidewire lever of the endoscope. A receiving chamber receives pressurized fluid from a pump to impart a pressurized fluid biasing force that displaces the plunger relative to the actuator housing in a first direction and a return actuator that imparts a return biasing force that displaces the plunger relative to the actuator housing in a second direction. A controller controls the pump to provide the pressurized fluid at a first pressure at which the pressurized fluid biasing force is greater than the return biasing force to displace the plunger lever in the first direction and a second pressure at which the return biasing force is greater than the pressurized fluid biasing force to displace the plunger and the lever in the second direction.
A61B 1/12 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with cooling or rinsing arrangements
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.
A61B 90/70 - Cleaning devices specially adapted for surgical instruments
A61B 1/012 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor characterised by internal passages or accessories therefor
G01N 21/78 - Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator producing a change of colour
A pinch valve includes a housing, first and second pinch bars, an actuator, a first front roller and a first rear roller. The actuator translates the first and second pinch bars relative to one another along a translation axis to pinch a flexible tube extending through an opening of the housing. The first front roller and the first rear roller are spaced from one another in the direction of a longitudinal axis. The first front roller extends transverse the opening and is positioned longitudinally upstream from the first and second pinch bars and the first rear roller extends transverse the opening and is positioned longitudinally downstream from the first and second pinch bars. The housing includes a first wall bordering the opening. A first plane lying tangent to the first front roller and the first rear roller is spaced inward from the first wall of the housing.
A system includes a surgical lighthead including a lighthead housing including a plurality of light emitting elements therein that are arranged to emit light toward to a region of interest, and a handle attached to the lighthead housing. A sensor is integrated with the lighthead and configured to measure an ambient environmental condition at the lighthead. In other embodiments, a medical device support system includes a support and an ambient environmental condition sensor assembly coupled to the support column and including a sensor configured to measure an ambient environmental condition at the ambient environmental condition sensor assembly. A controller is operatively coupled to the sensor and configured to detect an ambient environmental condition based at least in part on the measured ambient environmental condition by the sensor.
A surgical lighting system includes a surgical lighthead including a lighthead housing including one or more light emitting elements therein that are arranged to emit light toward a region of interest. In some embodiments a temperature sensor is mounted to the lighthead housing and arranged such that it measures the temperature of a location in the region of interest. In other embodiments, a temperature sensor is external to the lighthead and configured to measure the temperature of a location in the region of interest. A controller is operatively coupled to the temperature sensor and configured to control temperature at the region of interest based at least in part on the temperature measured by the temperature sensor.
A surgical lighting system includes a surgical lighthead including a lighthead housing including one or more light emitting elements therein that are arranged to emit light toward a region of interest. In some embodiments a temperature sensor is mounted to the lighthead housing and arranged such that it measures the temperature of a location in the region of interest. In other embodiments, a temperature sensor is external to the lighthead and configured to measure the temperature of a location in the region of interest. A controller is operatively coupled to the temperature sensor and configured to control temperature at the region of interest based at least in part on the temperature measured by the temperature sensor.
A system includes a surgical lighthead including a lighthead housing including a plurality of light emitting elements therein that are arranged to emit light toward to a region of interest, and a handle attached to the lighthead housing. A sensor is integrated with the lighthead and configured to measure an ambient environmental condition at the lighthead. In other embodiments, a medical device support system includes a support and an ambient environmental condition sensor assembly coupled to the support column and including a sensor configured to measure an ambient environmental condition at the ambient environmental condition sensor assembly. A controller is operatively coupled to the sensor and configured to detect an ambient environmental condition based at least in part on the measured ambient environmental condition by the sensor.
A positioning aid that is attachable to a handle of an endoscope control handle having air/water and suction valve cylinder ports and operable to guide a tool into at least one of the air/water or suction valve ports has a body for coupling to the endoscope control handle, the body including at least one guide port. The guide port includes an input port for receiving an instrument to be inserted into the air/water or suction valve cylinder ports, an output port configured to correspond with one of the air/water or suction valve cylinder ports, and a guide channel coupled between the input port and the output port.
A61B 1/00 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
A61B 1/12 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with cooling or rinsing arrangements
26.
SURGICAL LIGHTING SYSTEM CO-ILLUMINATION DETECTION
A device and method for operating a lighting system varies a characteristic of visible light emitted by a first lighthead according to a predefined profile, and fixes a characteristic of visible light emitted by a second lighthead. A light sensor configured to view a focal area of the second lighthead detects a characteristic of visible light on a target surface over a period of time, and the characteristic of the light detected by the light sensor over the period of time is compared to the characteristic of light defined in the predetermined profile. A mode of operation of the first and second lighthead is determined based on the comparison.
A device and method for operating a lighting system varies a characteristic of visible light emitted by a first lighthead according to a predefined profile, and fixes a characteristic of visible light emitted by a second lighthead. A light sensor configured to view a focal area of the second lighthead detects a characteristic of visible light on a target surface over a period of time, and the characteristic of the light detected by the light sensor over the period of time is compared to the characteristic of light defined in the predetermined profile. A mode of operation of the first and second lighthead is determined based on the comparison.
A single-step absorbent wipe for cleaning and disinfecting medical instruments includes various active ingredients as well as compounds that increase the efficacy profile of the product against various organisms, improve the buffering capacity of the formulation, enhance the antimicrobial efficacy against mycobacteria, increases the wetting and cleaning profile of the formulation, as well as adjusts the pH thereof. The disinfectant wipe provides a procedure to suitably clean and intermediate level disinfect medical instruments that are heat liable as well as non-submersible.
A single-step absorbent wipe for cleaning and disinfecting medical instruments includes various active ingredients as well as compounds that increase the efficacy profile of the product against various organisms, improve the buffering capacity of the formulation, enhance the antimicrobial efficacy against mycobacteria, increases the wetting and cleaning profile of the formulation, as well as adjusts the pH thereof. The disinfectant wipe provides a procedure to suitably clean and intermediate level disinfect medical instruments that are heat liable as well as non-submersible.
A single-step absorbent wipe for cleaning and disinfecting medical instruments includes various active ingredients as well as compounds that increase the efficacy profile of the product against various organisms, improve the buffering capacity of the formulation, enhance the antimicrobial efficacy against mycobacteria, increases the wetting and cleaning profile of the formulation, as well as adjusts the pH thereof. The disinfectant wipe provides a procedure to suitably clean and intermediate level disinfect medical instruments that are heat liable as well as non-submersible.
A load balancing arm for a medical device support system includes a proximal hub, a support arm, first and second springs, and a link. The link has a proximal end pivotably mounted to a link bearing element for pivotable movement about a link pivot axis, and a distal end pivotably mounted to a distal end of the first spring and a proximal end of the second spring. The link and first and second springs are configured such that the biasing forces exerted by the first and second springs are transmitted through the link to the link bearing element thereby to generate a moment about a main pivot axis of a proximal hub that counters a moment generated by a medical device load at a distal end of the support arm.
A load balancing arm for a medical device support system includes a proximal hub, a support arm, first and second springs, and a link. The link has a proximal end pivotably mounted to a link bearing element for pivotable movement about a link pivot axis, and a distal end pivotably mounted to a distal end of the first spring and a proximal end of the second spring. The link and first and second springs are configured such that the biasing forces exerted by the first and second springs are transmitted through the link to the link bearing element thereby to generate a moment about a main pivot axis of a proximal hub that counters a moment generated by a medical device load at a distal end of the support arm.
A load balancing arm for a medical device support system includes a proximal hub, a support arm, first and second springs, and a link. The link has a proximal end pivotably mounted to a link bearing element for pivotable movement about a link pivot axis, and a distal end pivotably mounted to a distal end of the first spring and a proximal end of the second spring. The link and first and second springs are configured such that the biasing forces exerted by the first and second springs are transmitted through the link to the link bearing element thereby to generate a moment about a main pivot axis of a proximal hub that counters a moment generated by a medical device load at a distal end of the support arm.
F16M 13/02 - Other supports for positioning apparatus or articles; Means for steadying hand-held apparatus or articles for supporting on, or attaching to, an object, e.g. tree, gate, window-frame, cycle
34.
Knuckle joint assembly for medical device support system
Knuckle joint assembly for a medical device support system. The knuckle joint assembly includes a cartridge assembly that includes a cartridge housing and a rotary bearing. The cartridge housing includes a bore having a central axis and a bearing mount in the bore. The rotary bearing is press fitted in the bearing mount and configured to receive axially therethrough a spindle to rotatably support the spindle about the central axis. The knuckle joint assembly includes a retaining clip and a retaining pin. The retaining clip is selectively movable to disengage and engage a groove in a spindle to respectively support or release the spindle along a central axis. The retaining pin is movable between a first position to allow movement of the retaining clip between positions but prevent removal of the retaining clip, and a second position to block movement of the retaining clip from the engaged position.
A61B 90/50 - Supports for surgical instruments, e.g. articulated arms
F16M 13/02 - Other supports for positioning apparatus or articles; Means for steadying hand-held apparatus or articles for supporting on, or attaching to, an object, e.g. tree, gate, window-frame, cycle
A decontamination system, method, and sterilant kit for a device, such as a lumen device, is depicted. The decontamination system, in some embodiments, includes a device container, a wicking pad, and a sterilant fluid delivery device. The device container, such as a terminal package or a decontamination chamber, defines a device receiving area. The wicking pad is in fluid communication with the device receiving area. The sterilant fluid delivery device is in fluid communication with the wicking pad. The sterilant fluid delivery device is configured to wet the wicking pad with sterilant fluid. The wicking pad is configured to evaporate sterilant fluid into the device receiving area.
A sterilization challenge device for verifying the efficacy of a gas sterilization process includes an outer container, an inner container, a chemical indicator, and a cap. The outer container includes an open end, a closed end, a chamber configured to contain the inner container containing the chemical indicator, and at least one hole arranged proximate the open end. The cap is configured to engage with the outer container to close the open end, and the at least one hole is configured to provide a flow path for the gaseous sterilant into the chamber.
A sterilization challenge device for verifying the efficacy of a gas sterilization process includes an outer container, an inner container, a chemical indicator, and a cap. The outer container includes an open end, a closed end, a chamber configured to contain the inner container containing the chemical indicator, and at least one hole arranged proximate the open end. The cap is configured to engage with the outer container to close the open end, and the at least one hole is configured to provide a flow path for the gaseous sterilant into the chamber.
A sterilization challenge device for verifying the efficacy of a gas sterilization process includes an outer container, an inner container, a chemical indicator, and a cap. The outer container includes an open end, a closed end, a chamber configured to contain the inner container containing the chemical indicator, and at least one hole arranged proximate the open end. The cap is configured to engage with the outer container to close the open end, and the at least one hole is configured to provide a flow path for the gaseous sterilant into the chamber.
G01N 31/22 - Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroups; Apparatus specially adapted for such methods using chemical indicators
A61L 9/04 - Disinfection, sterilisation or deodorisation of air using gaseous or vaporous substances, e.g. ozone using substances evaporated in the air without heating
Dynamic systems and methods for fixed noise pattern calibrations and image corrections are provided. Imaging devices may be calibrated via the system by adjusting an imaging sensor exposure to acquire one or more black images. A global average pixel value is calculated to accumulate pixel values per column of the acquired image. The calculated global average pixel value is then saved as offset imaging data. An average pixel value per column of the imaging data based on the accumulated pixel values may also be calculated, and stored as offset imaging data. A correction matrix may be recomposed based on the offset imaging data and used for calibrating the imaging sensor, and for creating corrected images in or near real time.
Dynamic systems and methods for fixed noise pattern calibrations and image corrections are provided. Imaging devices may be calibrated via the system by adjusting an imaging sensor exposure to acquire one or more black images. A global average pixel value is calculated to accumulate pixel values per column of the acquired image. The calculated global average pixel value is then saved as offset imaging data. An average pixel value per column of the imaging data based on the accumulated pixel values may also be calculated, and stored as offset imaging data. A correction matrix may be recomposed based on the offset imaging data and used for calibrating the imaging sensor, and for creating corrected images in or near real time.
Dynamic systems and methods for fixed noise pattern calibrations and image corrections are provided. Imaging devices may be calibrated via the system by adjusting an imaging sensor exposure to acquire one or more black images. A global average pixel value is calculated to accumulate pixel values per column of the acquired image. The calculated global average pixel value is then saved as offset imaging data. An average pixel value per column of the imaging data based on the accumulated pixel values may also be calculated, and stored as offset imaging data. A correction matrix may be recomposed based on the offset imaging data and used for calibrating the imaging sensor, and for creating corrected images in or near real time.
This invention relates to a chemical indicator, comprising: a non-cellulosic backing layer; a non-cellulosic cover layer overlying the backing layer; the backing layer and/or the cover layer comprising a gas permeable polymeric film; a non-cellulosic wicking material positioned between the backing layer and the cover layer; a dye composition positioned between the backing layer and the cover layer and in contact with or nearly in contact with the wicking strip, the dye composition comprising an indicator dye which changes color in the presence of hydrogen peroxide, and a base medium, which melts at a temperature in the range from about 45° C. to about 65° C.; the cover layer including a transparent portion to permit observation of the wicking material; and an adhesive for adhering the cover layer to the backing layer. The chemical indicator may be referred to as a moving front chemical indicator. A process for conducting a vaporous hydrogen peroxide (VHP) sterilization process using the foregoing chemical indicator is disclosed.
G01N 21/78 - Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator producing a change of colour
G01N 31/22 - Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroups; Apparatus specially adapted for such methods using chemical indicators
A non-aspirating dispenser containing a gel therein for delivery to a desired surface such as a medical article. More specifically, a gel that is dispensed in the form of droplets that are free of air or a gas therein and with reduced drift potential. The dispenser has a container having a flexible bag therein enclosing a thixotropic gel, and has a pressurized gas that is capable of exerting pressure on the bag and forcing the gel out of said bag in a steady stream upon pressing an actuator that is operatively connected to an ejection valve. The bag is free of propellants, and does not produce an aerosol. The gel is thixotropic and is utilized for keeping medical instruments moist in order to prevent soils present thereon from drying out, which can make reprocessing of medical instruments more difficult and less effective. The dispenser implemented at a point of use for transport or prior to delayed reprocessing in the reprocessing area.
B65D 35/28 - Pliable tubular containers adapted to be permanently deformed to expel contents, e.g. collapsible tubes for toothpaste or other plastic or semi-liquid material; Holders therefor with auxiliary devices for expelling contents
B65D 83/14 - Containers or packages with special means for dispensing contents for delivery of liquid or semi-liquid contents by internal gaseous pressure, i.e. aerosol containers comprising propellant
B65D 83/62 - Contents and propellant separated by membrane, bag, or the like
44.
SURGICAL LIGHTING SYSTEM THAT REDUCES RISK OF EXCESSIVE RADIANT ENERGY
A light system monitors an area of interest for exposure to radiant energy provided by an operating room light head. At least one operating parameter of the light head is obtained, and based on the at least one operating parameter it is determined if the area of interest has been or will be exposed to radiant energy exceeding a prescribed threshold over a prescribed time period. Based on the determination, the system at least one of automatically adjusts an operating setting of the at least one light head or generates a warning of possible overexposure to radiant energy in the area of interest.
A steam sterilizer having a door movable relative to an opening between a first open position and a second closed position. A plurality of spaced-apart roller assemblies are aligned along edges of the door to align the door relative to the opening as the door moves between the open and closed position. Each of the roller assemblies are comprised of a cylindrical roller having an outer annual recess extending along the periphery thereof. The recess is dimensioned to receive a lateral edge of the door. The roller is mounted on a shaft and is movable against a biasing force axially along the axis of the shaft.
E06B 7/20 - Sealing arrangements on wings or parts co-operating with the wings by means of movable edgings, e.g. draught sealings additionally used for bolting automatically withdrawn when the wing is opened
E05D 15/16 - Suspension arrangements for wings for wings sliding vertically more or less in their own plane
A light system monitors an area of interest for exposure to radiant energy provided by an operating room light head. At least one operating parameter of the light head is obtained, and based on the at least one operating parameter it is determined if the area of interest has been or will be exposed to radiant energy exceeding a prescribed threshold over a prescribed time period. Based on the determination, the system at least one of automatically adjusts an operating setting of the at least one light head or generates a warning of possible overexposure to radiant energy in the area of interest.
A light system monitors an area of interest for exposure to radiant energy provided by an operating room light head. At least one operating parameter of the light head is obtained, and based on the at least one operating parameter it is determined if the area of interest has been or will be exposed to radiant energy exceeding a prescribed threshold over a prescribed time period. Based on the determination, the system at least one of automatically adjusts an operating setting of the at least one light head or generates a warning of possible overexposure to radiant energy in the area of interest.
A medical device support system including a shaft, an extension arm, and a hub mounted to the shaft for pivotable movement of the extension arm about a rotation axis of the shaft. The hub includes a cavity including first and second contact faces, and at least one floating stop movably disposed in the cavity. The hub is pivotably mounted for a range of at least 360-degrees rotation about the rotation axis. The at least 360-degrees rotation range is based on a compound of a first rotation range and a second rotation range. The first rotation range is defined by a first movable amount of the at least one floating stop between first and second stop surfaces fixed relative to the shaft. The second rotation range is defined by a second movable amount of the at least one floating stop between the first and second contact faces of the hub.
A61B 90/50 - Supports for surgical instruments, e.g. articulated arms
A61G 12/00 - Accommodation for nursing, e.g. in hospitals, not covered by groups , e.g. trolleys for transport of medicaments or food; Prescription lists
F16D 49/08 - Brakes with a braking member co-operating with the periphery of a drum, wheel-rim, or the like shaped as an encircling band extending over approximately 360°
49.
MEDICAL DEVICE SUPPORT SYSTEM INCLUDING ROTATIONAL CONTROL MECHANISM
A medical device support system including a shaft, extension arm, and floating stop. A guide channel member is fixed to the shaft and includes an elongated cavity that defines first and second contact faces at its opposite ends. A hub of the extension arm is pivotably mounted for a range of at least 360 degrees rotation about a rotation axis of the shaft. The at least 360 degrees rotation range is based on a compound of a first rotation range and a second rotation range. The first rotation range is defined by a fixed stop of the hub configured to move between first and second contact faces of a radially outer portion of the floating stop. The second rotation range is defined by a radially inner portion of the floating stop configured to move between the first and second contact faces of the elongated cavity of the guide channel member.
A61B 90/50 - Supports for surgical instruments, e.g. articulated arms
A61G 12/00 - Accommodation for nursing, e.g. in hospitals, not covered by groups , e.g. trolleys for transport of medicaments or food; Prescription lists
F16D 49/08 - Brakes with a braking member co-operating with the periphery of a drum, wheel-rim, or the like shaped as an encircling band extending over approximately 360°
50.
MEDICAL DEVICE SUPPORT SYSTEM INCLUDING ROTATIONAL CONTROL MECHANISM
A medical device support system including a shaft, extension arm, and floating stop. A guide channel member is fixed to the shaft and includes an elongated cavity that defines first and second contact faces at its opposite ends. A hub of the extension arm is pivotably mounted for a range of at least 360 degrees rotation about a rotation axis of the shaft. The at least 360 degrees rotation range is based on a compound of a first rotation range and a second rotation range. The first rotation range is defined by a fixed stop of the hub configured to move between first and second contact faces of a radially outer portion of the floating stop. The second rotation range is defined by a radially inner portion of the floating stop configured to move between the first and second contact faces of the elongated cavity of the guide channel member.
A61G 12/00 - Accommodation for nursing, e.g. in hospitals, not covered by groups , e.g. trolleys for transport of medicaments or food; Prescription lists
A61B 90/50 - Supports for surgical instruments, e.g. articulated arms
F16D 49/08 - Brakes with a braking member co-operating with the periphery of a drum, wheel-rim, or the like shaped as an encircling band extending over approximately 360°
51.
MEDICAL DEVICE SUPPORT SYSTEM INCLUDING ROTATIONAL CONTROL MECHANISM
A medical device support system including a shaft, an extension arm, and a free rotating ring. The shaft includes an elongated peripheral cavity that defines first and second contact faces at opposite peripheral ends. A hub of the extension arm is pivotably mounted for a range of at least 360 degrees rotation about a rotation axis of the shaft. The at least 360 degrees rotation range is based on a compound of a first rotation range and a second rotation range. The first rotation range is defined by a fixed stop of the hub configured to move between first and second contact faces of a radially outward protruding member of the free rotating ring. The second rotation range is defined by a radially inward protruding member of the free rotating ring configured to move between the first and second contact faces of the elongated peripheral cavity of the shaft.
A61B 90/40 - Apparatus fixed or close to patients specially adapted for providing an aseptic surgical environment
A61G 12/00 - Accommodation for nursing, e.g. in hospitals, not covered by groups , e.g. trolleys for transport of medicaments or food; Prescription lists
52.
MEDICAL DEVICE SUPPORT SYSTEM INCLUDING ROTATIONAL CONTROL MECHANISM
A medical device support system including a shaft, an extension arm, and a free rotating ring. The shaft includes an elongated peripheral cavity that defines first and second contact faces at opposite peripheral ends. A hub of the extension arm is pivotably mounted for a range of at least 360 degrees rotation about a rotation axis of the shaft. The at least 360 degrees rotation range is based on a compound of a first rotation range and a second rotation range. The first rotation range is defined by a fixed stop of the hub configured to move between first and second contact faces of a radially outward protruding member of the free rotating ring. The second rotation range is defined by a radially inward protruding member of the free rotating ring configured to move between the first and second contact faces of the elongated peripheral cavity of the shaft.
A61G 12/00 - Accommodation for nursing, e.g. in hospitals, not covered by groups , e.g. trolleys for transport of medicaments or food; Prescription lists
A61B 90/40 - Apparatus fixed or close to patients specially adapted for providing an aseptic surgical environment
53.
MEDICAL DEVICE SUPPORT SYSTEM INCLUDING ROTATIONAL CONTROL MECHANISM
A medical device support system including a shaft, an extension arm, and a hub mounted to the shaft for pivotable movement of the extension arm about a rotation axis of the shaft. The hub includes a cavity including first and second contact faces, and at least one floating stop movably disposed in the cavity. The hub is pivotably mounted for a range of at least 360-degrees rotation about the rotation axis. The at least 360-degrees rotation range is based on a compound of a first rotation range and a second rotation range. The first rotation range is defined by a first movable amount of the at least one floating stop between first and second stop surfaces fixed relative to the shaft. The second rotation range is defined by a second movable amount of the at least one floating stop between the first and second contact faces of the hub.
A61G 12/00 - Accommodation for nursing, e.g. in hospitals, not covered by groups , e.g. trolleys for transport of medicaments or food; Prescription lists
A61B 90/50 - Supports for surgical instruments, e.g. articulated arms
F16D 49/08 - Brakes with a braking member co-operating with the periphery of a drum, wheel-rim, or the like shaped as an encircling band extending over approximately 360°
54.
CHEMICAL INJECTION AND METERING MODULE FOR STERILIZATION SYSTEM
The present disclosure discusses a sterilization system having a dosing module with a dosing cylinder to allow for metered flow of a predetermined amount of sterilant fluid into the sterilization system. The dosing module can include a dosing cylinder for measuring the predetermined amount of sterilant fluid, a pump for moving the sterilant fluid, and a controller configured to initiate driving of the sterilant fluid through the dosing module and into the sterilization system. A method of providing a predetermined amount of sterilant fluid to the sterilization system can include controlling the flow of sterilant fluid into the dosing cylinder, measuring the amount of sterilant fluid in the dosing cylinder to a desired dose amount, and controlling flow of the dose into the sterilization system.
A61L 2/24 - Apparatus using programmed or automatic operation
A61L 2/00 - Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
A61L 2/02 - Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using physical phenomena
A61L 2/16 - Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using chemical substances
55.
MEDICAL DEVICE SUPPORT SYSTEM INCLUDING ROTATIONAL CONTROL MECHANISM
A medical device support system including a shaft, an extension arm, and a free rotating ring. The shaft includes an elongated peripheral cavity that defines first and second contact faces at opposite peripheral ends. A hub of the extension arm is pivotably mounted for a range of at least 360 degrees rotation about a rotation axis of the shaft. The at least 360 degrees rotation range is based on a compound of a first rotation range and a second rotation range. The first rotation range is defined by a fixed stop of the hub configured to move between first and second contact faces of a radially outward protruding member of the free rotating ring. The second rotation range is defined by a radially inward protruding member of the free rotating ring configured to move between the first and second contact faces of the elongated peripheral cavity of the shaft.
A61B 90/50 - Supports for surgical instruments, e.g. articulated arms
A61B 90/00 - Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups , e.g. for luxation treatment or for protecting wound edges
56.
MEDICAL DEVICE SUPPORT SYSTEM INCLUDING ROTATIONAL CONTROL MECHANISM
A medical device support system including a shaft, extension arm, and floating stop. A guide channel member is fixed to the shaft and includes an elongated cavity that defines first and second contact faces at its opposite ends. A hub of the extension arm is pivotably mounted for a range of at least 360 degrees rotation about a rotation axis of the shaft. The at least 360 degrees rotation range is based on a compound of a first rotation range and a second rotation range. The first rotation range is defined by a fixed stop of the hub configured to move between first and second contact faces of a radially outer portion of the floating stop. The second rotation range is defined by a radially inner portion of the floating stop configured to move between the first and second contact faces of the elongated cavity of the guide channel member.
A medical device support system including a shaft, an extension arm, and a hub mounted to the shaft for pivotable movement of the extension arm about a rotation axis of the shaft. The hub includes a cavity including first and second contact faces, and at least one floating stop movably disposed in the cavity. The hub is pivotably mounted for a range of at least 360-degrees rotation about the rotation axis. The at least 360-degrees rotation range is based on a compound of a first rotation range and a second rotation range. The first rotation range is defined by a first movable amount of the at least one floating stop between first and second stop surfaces fixed relative to the shaft. The second rotation range is defined by a second movable amount of the at least one floating stop between the first and second contact faces of the hub.
F21V 21/28 - Pivoted arms adjustable in more than one plane
A61B 90/00 - Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups , e.g. for luxation treatment or for protecting wound edges
58.
Lighting assemblies for medical device suspension system
Embodiments include a lighting assembly includes an elongate gasket body formed of a resilient, optically transmissive material. The gasket body includes a light source cavity at least partially defined by a light transmission portion and an attachment channel configured to attach the gasket body to a mount. A light source is disposed in the light source cavity. Other embodiments include securement ring including a clamp portion and a lighting assembly portion. The clamp portion includes first and second segments, each being semiannular in shape and curving between first and second ends, the first end of the first segment coupled to the second end of the second segment and the second end of the first segment coupled to the first end of the second segment to collectively form an aperture. The lighting assembly portion includes a first and second segments, each being semiannular in shape and including a light source.
A load balancing arm (20) for a medical device support system includes a proximal hub (22, 120, 114), a support arm (50), a link (90), and a distal end vertical block (112). The components together form a four bar linkage. The proximal hub is configured for pivotable movement about an axis P-P. A distal hub (122) is configured to support a medical device load for pivotable movement about an axis D-D. The distal hub (122) is mounted to the distal end vertical block(112) for pivotable movement between a first position in which the axis D-D is at a first angle relative to the axis P-P and a second position in which the axis D-D is at a second angle relative to the axis P-P, wherein the first angle is different than the second angle. A parallelism adjustment mechanism enables the axis D-D to be adjusted so as to be substantially parallel to the axis P-P.
A61G 12/00 - Accommodation for nursing, e.g. in hospitals, not covered by groups , e.g. trolleys for transport of medicaments or food; Prescription lists
60.
PARALLELISM ADJUSTMENT MECHANISM FOR LOAD BALANCING ARM
A load balancing arm (20) for a medical device support system includes a proximal hub (22, 120, 114), a support arm (50), a link (90), and a distal end vertical block (112). The components together form a four bar linkage. The proximal hub is configured for pivotable movement about an axis P-P. A distal hub (122) is configured to support a medical device load for pivotable movement about an axis D-D. The distal hub (122) is mounted to the distal end vertical block(112) for pivotable movement between a first position in which the axis D-D is at a first angle relative to the axis P-P and a second position in which the axis D-D is at a second angle relative to the axis P-P, wherein the first angle is different than the second angle. A parallelism adjustment mechanism enables the axis D-D to be adjusted so as to be substantially parallel to the axis P-P.
A61G 12/00 - Accommodation for nursing, e.g. in hospitals, not covered by groups , e.g. trolleys for transport of medicaments or food; Prescription lists
61.
PARALLELISM ADJUSTMENT MECHANISM FOR LOAD BALANCING ARM
A load balancing arm for a medical device support system includes a proximal hub, a support arm, a link, and a distal end vertical block. The components together may form a four bar linkage. The proximal hub is configured for pivotable movement about an axis P-P. The distal hub is configured to support a medical device load for pivotable movement about an axis D-D. The distal hub is mounted to the distal end vertical block for pivotable movement between a first position in which the axis D-D is at a first angle relative to the axis P-P and a second position in which the axis D-D is at a second angle relative to the axis P-P, wherein the first angle is different than the second angle. A parallelism adjustment mechanism enables the axis D-D to be adjusted so as to be substantially parallel to the axis P-P.
A sterilization challenge device for verifying the efficacy of a sterilization process includes a container, an insert member, a sterilization indicator, and a cap. The container includes an open end, a closed end, a chamber configured to contain the biological indicator and the insert member, and at least one hole arranged proximate the open end. The cap is configured to engage with the container to close the open end, and the at least one hole is configured to provide a flow path for the gaseous sterilant into the chamber.
A61L 2/28 - Devices for testing the effectiveness or completeness of sterilisation, e.g. indicators which change colour
A61B 50/30 - Containers specially adapted for packaging, protecting, dispensing, collecting or disposing of surgical or diagnostic appliances or instruments
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.
A61B 1/00 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
A61B 1/12 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with cooling or rinsing arrangements
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.
A61B 90/70 - Cleaning devices specially adapted for surgical instruments
A61B 1/012 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor characterised by internal passages or accessories therefor
G01N 21/78 - Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator producing a change of colour
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.
A61B 1/00 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor
A61B 1/12 - Instruments for performing medical examinations of the interior of cavities or tubes of the body by visual or photographical inspection, e.g. endoscopes; Illuminating arrangements therefor with cooling or rinsing arrangements
A sterilization challenge device (10) for verifying the efficacy of a sterilization process includes a container (12), an insert member (16), a sterilization indicator (18), and a cap (14). The container (12) includes an open end (22), a closed end (24), a chamber (20) configured to contain the biological indicator (18) and the insert member (16), and at least one hole (36) arranged proximate the open end (22). The cap (14) is configured to engage with the container (12) to close the open end (22), and the at least one hole (36) is configured to provide a flow path for the gaseous sterilant into the chamber (20).
A sterilization challenge device (10) for verifying the efficacy of a sterilization process includes a container (12), an insert member (16), a sterilization indicator (18), and a cap (14). The container (12) includes an open end (22), a closed end (24), a chamber (20) configured to contain the biological indicator (18) and the insert member (16), and at least one hole (36) arranged proximate the open end (22). The cap (14) is configured to engage with the container (12) to close the open end (22), and the at least one hole (36) is configured to provide a flow path for the gaseous sterilant into the chamber (20).
A decontamination system for a lumen device is depicted. The decontamination system, in some embodiments, includes a lumen device container, a pump, and a sealed container with decontamination fluid. The lumen device container defines a lumen device receiving area. The pump is configured to reduce pressure within the lumen device receiving area. The sealed container is configured to release the decontamination fluid into the lumen device receiving area responsive to a pressure drop applied to the sealed container.
A sterilization process test device for verifying the efficacy of a sterilization process includes a tubular body defining a chamber for containing at least one sterilization indicator and a cap to sealingly close the tubular body. The tubular body includes at least one hole, which is covered by a gas and steam permeable cover. The only flow path into the chamber is provided through the steam and gas permeable cover and the at least one hole, which when combined are configured to control and restrict a flow of steam or a gaseous sterilization medium from an external environment.
A sterilization process test device for verifying the efficacy of a sterilization process includes a tubular body defining a chamber for containing at least one sterilization indicator and a cap to sealingly close the tubular body. The tubular body includes at least one hole, which is covered by a gas and steam permeable cover. The only flow path into the chamber is provided through the steam and gas permeable cover and the at least one hole, which when combined are configured to control and restrict a flow of steam or a gaseous sterilization medium from an external environment.
A method and apparatus for reprocessing decontaminating articles in a steam sterilizer at low temperatures and sub-atmospheric pressure. The method includes steps for operating the steam sterilizer such that it can safely and effectively decontaminate articles at temperatures below conventional steam sterilization processing temperatures. The steam sterilizer includes a low temperature operating mode that processes articles in a chamber at low temperatures and at sub-atmospheric pressure.
A sterilization process test device for verifying the efficacy of a sterilization process includes a tubular body defining a chamber for containing at least one sterilization indicator and a cap to sealingly close the tubular body. The tubular body includes at least one hole, which is covered by a gas and steam permeable cover. The only flow path into the chamber is provided through the steam and gas permeable cover and the at least one hole, which when combined are configured to control and restrict a flow of steam or a gaseous sterilization medium from an external environment.
A method and apparatus for reprocessing decontaminating articles in a steam sterilizer at low temperatures and sub-atmospheric pressure. The method includes steps for operating the steam sterilizer such that it can safely and effectively decontaminate articles at temperatures below conventional steam sterilization processing temperatures. The steam sterilizer includes a low temperature operating mode that processes articles in a chamber at low temperatures and at sub-atmospheric pressure.
Various examples disclosed relate to a device for use in a disinfection process. The device can include, for example, a sampling assembly capable of a first position and a second position, wherein the sampling assembly is configured to be used inside a sterilization system. The sampling assembly can include a top portion, a bottom portion, at least one seal therebetween such that the top portion and the bottom portion form an airtight compartment when in the first position, a central pin running through the top portion and bottom portion, and an actuator configured to move the sampling assembly between the first position and the second position along the central pin during a portion of the disinfection process, such that the sampling assembly can collect a sample of atmosphere within the disinfection system.
A method and apparatus for reprocessing decontaminating articles in a steam sterilizer at low temperatures and sub-atmospheric pressure. The method includes steps for operating the steam sterilizer such that it can safely and effectively decontaminate articles at temperatures below conventional steam sterilization processing temperatures. The steam sterilizer includes a low temperature operating mode that processes articles in a chamber at low temperatures and at sub-atmospheric pressure.
A surgical lighting system and a method of rotating a camera of a surgical lighting system includes a light head housing including a plurality of light emitting elements arranged to emit light downward to a region of interest, a handle mounted to and protruding downward from the light head housing, the handle including a handle housing having a sufficient size to be gripped by the human hand, and a camera assembly mounted within the handle housing and including a camera having a field of view that encompasses at least a portion of the region of interest. The camera assembly is mounted within the handle housing for rotation greater than 360 degrees about a rotation axis from a first stop to a second stop and vice versa. The first stop limits clockwise rotation of the camera and the second stop limits counterclockwise rotation of the camera.
A surgical lighting system includes a central shaft, a surgical light head, an extension arm, a load balancing arm, and a yoke assembly. The extension arm is pivotably mounted to the central shaft. The load balancing arm is pivotably mounted to the extension arm. The yoke assembly supports the light head for multi-axis movement relative to the load balancing arm. The surgical light head includes a plurality of light emitting elements that are arranged to emit light downward to a region of interest and an optical signal generating component configured to capture data associated with the region of interest and generate an optical signal based on the captured data. Optical fiber cables and rotatable joints transmit the optical signal associated with the captured data from the surgical light head to one or more of the yoke assembly, the load balancing arm, the extension arm, and the central shaft.
A surgical lighting system and a method of rotating a camera of a surgical lighting system includes a light head housing including a plurality of light emitting elements arranged to emit light downward to a region of interest, a handle mounted to and protruding downward from the light head housing, the handle including a handle housing having a sufficient size to be gripped by the human hand, and a camera assembly mounted within the handle housing and including a camera having a field of view that encompasses at least a portion of the region of interest. The camera assembly is mounted within the handle housing for rotation greater than 360 degrees about a rotation axis from a first stop to a second stop and vice versa. The first stop limits clockwise rotation of the camera and the second stop limits counterclockwise rotation of the camera.
A surgical lighting system includes a central shaft, a surgical light head, an extension arm, a load balancing arm, and a yoke assembly. The extension arm is pivotably mounted to the central shaft. The load balancing arm is pivotably mounted to the extension arm. The yoke assembly supports the light head for multi-axis movement relative to the load balancing arm. The surgical light head includes a plurality of light emitting elements that are arranged to emit light downward to a region of interest and an optical signal generating component configured to capture data associated with the region of interest and generate an optical signal based on the captured data. Optical fiber cables and rotatable joints transmit the optical signal associated with the captured data from the surgical light head to one or more of the yoke assembly, the load balancing arm, the extension arm, and the central shaft.
A61B 90/30 - Devices for illuminating a surgical field, the devices having an interrelation with other surgical devices or with a surgical procedure
A61B 90/00 - Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups , e.g. for luxation treatment or for protecting wound edges
A61B 17/00 - Surgical instruments, devices or methods, e.g. tourniquets
81.
LIGHT HEAD HAVING CAMERA ASSEMBLY INTEGRATED IN HANDLE AND SURGICAL LIGHTING SYSTEM INCLUDING SAME
A surgical lighting system includes a light head housing, a handle, a camera, and an optical fiber cable. The light head housing includes a plurality of light emitting elements therein that are arranged to emit light downward to a region of interest. The handle is mounted to the light head housing and protrudes downward from the light head housing, the handle including a handle housing having a sufficient size to be gripped by the human hand. A camera is mounted within the handle housing, the camera having a field of view that encompasses at least a portion of the region of interest. An optical fiber cable extends from a location within the handle housing and to the light head housing, the optical fiber cable being configured to transmit optical video signals associated with video data captured by the camera to the light head housing.
A surgical lighting system and a method of rotating a camera of a surgical lighting system includes a light head housing including a plurality of light emitting elements arranged to emit light downward to a region of interest, a handle mounted to and protruding downward from the light head housing, the handle including a handle housing having a sufficient size to be gripped by the human hand, and a camera assembly mounted within the handle housing and including a camera having a field of view that encompasses at least a portion of the region of interest. The camera assembly is mounted within the handle housing for rotation greater than 360 degrees about a rotation axis from a first stop to a second stop and vice versa. The first stop limits clockwise rotation of the camera and the second stop limits counterclockwise rotation of the camera.
F21V 33/00 - Structural combinations of lighting devices with other articles, not otherwise provided for
G03B 15/14 - Special procedures for taking photographs; Apparatus therefor for taking photographs during medical operations
A61B 90/30 - Devices for illuminating a surgical field, the devices having an interrelation with other surgical devices or with a surgical procedure
A61B 90/00 - Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups , e.g. for luxation treatment or for protecting wound edges
G02B 6/38 - Mechanical coupling means having fibre to fibre mating means
G03B 30/00 - Camera modules comprising integrated lens units and imaging units, specially adapted for being embedded in other devices, e.g. mobile phones or vehicles
A surgical lighting system includes a light head housing, a handle, a camera, and an optical fiber cable. The light head housing includes a plurality of light emitting elements therein that are arranged to emit light downward to a region of interest. The handle is mounted to the light head housing and protrudes downward from the light head housing, the handle including a handle housing having a sufficient size to be gripped by the human hand. A camera is mounted within the handle housing, the camera having a field of view that encompasses at least a portion of the region of interest. An optical fiber cable extends from a location within the handle housing and to the light head housing, the optical fiber cable being configured to transmit optical video signals associated with video data captured by the camera to the light head housing.
A surgical lighting system includes a central shaft, a surgical light head, an extension arm, a load balancing arm, and a yoke assembly. The extension arm is pivotably mounted to the central shaft. The load balancing arm is pivotably mounted to the extension arm. The yoke assembly supports the light head for multi-axis movement relative to the load balancing arm. The surgical light head includes a plurality of light emitting elements that are arranged to emit light downward to a region of interest and an optical signal generating component configured to capture data associated with the region of interest and generate an optical signal based on the captured data. Optical fiber cables and rotatable joints transmit the optical signal associated with the captured data from the surgical light head to one or more of the yoke assembly, the load balancing arm, the extension arm, and the central shaft.
A61B 90/00 - Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups , e.g. for luxation treatment or for protecting wound edges
85.
INTERFACE/POUCH DESIGN FOR ASEPTIC OPENING OF STERILIZATION POUCH
A sterilizable pouch includes at least one sheet, wherein outer peripheral edges of the at least one sheet are sealed together to define a pouch having an interior space for receiving an article therein. A first releasable seam spans between a first peripheral edge of the at least one sheet to a second, opposite, peripheral edge of the at least one sheet, the first releasable seam dividing the at least one sheet into a first sheet part and a second sheet part. A second releasable seam and a third releasable seam each substantially span from a third peripheral edge of the at least one sheet to a fourth, opposite, peripheral edge of the at least one sheet and along the first peripheral edge and the second peripheral edge, respectively. The second and third releasable seams are arranged generally perpendicular to the first releasable seam, where the first, second and third releasable seams enable the pouch to be completely opened such that a device can be removed from the pouch without the device contacting non-sterile portions of the pouch.
A61B 50/30 - Containers specially adapted for packaging, protecting, dispensing, collecting or disposing of surgical or diagnostic appliances or instruments
A61B 50/36 - Containers specially adapted for packaging, protecting, dispensing, collecting or disposing of surgical or diagnostic appliances or instruments for collecting or disposing of used articles
86.
LIGHT HEAD HAVING CAMERA ASSEMBLY INTEGRATED IN HANDLE AND SURGICAL LIGHTING SYSTEM INCLUDING SAME
A surgical lighting system includes a light head housing, a handle, a camera, and an optical fiber cable. The light head housing includes a plurality of light emitting elements therein that are arranged to emit light downward to a region of interest. The handle is mounted to the light head housing and protrudes downward from the light head housing, the handle including a handle housing having a sufficient size to be gripped by the human hand. A camera is mounted within the handle housing, the camera having a field of view that encompasses at least a portion of the region of interest. An optical fiber cable extends from a location within the handle housing and to the light head housing, the optical fiber cable being configured to transmit optical video signals associated with video data captured by the camera to the light head housing.
A61B 90/30 - Devices for illuminating a surgical field, the devices having an interrelation with other surgical devices or with a surgical procedure
A61B 90/00 - Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups , e.g. for luxation treatment or for protecting wound edges
A61B 17/00 - Surgical instruments, devices or methods, e.g. tourniquets
87.
Interface/pouch design for aseptic opening of sterilization pouch
A sterilizable pouch includes at least one sheet, wherein outer peripheral edges of the at least one sheet are sealed together to define a pouch having an interior space for receiving an article therein. A first releasable seam spans between a first peripheral edge of the at least one sheet to a second, opposite, peripheral edge of the at least one sheet, the first releasable seam dividing the at least one sheet into a first sheet part and a second sheet part. A second releasable seam and a third releasable seam each substantially span from a third peripheral edge of the at least one sheet to a fourth, opposite, peripheral edge of the at least one sheet and along the first peripheral edge and the second peripheral edge, respectively. The second and third releasable seams are arranged generally perpendicular to the first releasable seam, where the first, second and third releasable seams enable the pouch to be completely opened such that a device can be removed from the pouch without the device contacting non-sterile portions of the pouch.
B65D 81/18 - Containers, packaging elements, or packages, for contents presenting particular transport or storage problems, or adapted to be used for non-packaging purposes after removal of contents providing specific environment for contents, e.g. temperature above or below ambient
A61B 50/30 - Containers specially adapted for packaging, protecting, dispensing, collecting or disposing of surgical or diagnostic appliances or instruments
B65D 33/18 - End- or aperture-closing arrangements or devices using adhesive applied to integral parts, e.g. to flaps
A light head for a medical device support system. The light head includes a housing base, an annular shape first lens, a housing cover, and a motion transfer member. The housing cover includes a cavity within which the annular shape first lens is rotatable about a rotation axis. The housing cover includes a second lens. The annular shape first lens and the second lens are in a light emitting path of the plurality of light emitting elements. The motion transfer member is configured to movably interact with a boss of the annular shape first lens to rotate the annular shape first lens about the rotation axis and within the cavity. A periphery of the annular shape first lens includes guide members configured to position the boss of the annular shape first lens to movably interact with the motion transfer member.
A light head for a medical device support system. The light head includes first and second zones of light sources, an optical system, and a control system. The first and second zones of light sources emit respective first and second beams of light that form an illumination pattern having a pattern size at a region of interest. The optical system adjusts a beam spread of the second beam of light to change the pattern size of the illumination pattern from a first pattern size to a second pattern size. The control system varies power to the first and second zones of light sources in response to adjustment of the beam spread of the second beam of light to maintain a substantially constant magnitude of illuminance at the region of interest as the pattern size is changed from the first pattern size to the second pattern size.
A heating element includes an electrically insulating layer; resistive layer formed of a positive temperature coefficient material; and an electrically conductive layer disposed between the electrically insulating layer and the resistive layer and including a first bus and a second bus that is spaced apart from the first bus, the resistive layer electrically connecting the first bus and the second bus. The electrically insulating layer, the electrically conductive layer, and the resistive layer are stacked to form a lamination and the lamination having a thickness and a width and length extending orthogonal to the thickness. The lamination may have slits extending through the thickness thereof and along a portion of the length thereof. Terminals may be connected to the buses and arranged to provide a counter current flow pattern across the lamination. The lamination may be used in a warming device and in connection with a patient warming system.
A light head for a medical device support system. The light head includes a housing base, an annular shape first lens, a housing cover, and a motion transfer member. The housing cover includes a cavity within which the annular shape first lens is rotatable about a rotation axis. The housing cover includes a second lens. The annular shape first lens and the second lens are in a light emitting path of the plurality of light emitting elements. The motion transfer member is configured to movably interact with a boss of the annular shape first lens to rotate the annular shape first lens about the rotation axis and within the cavity. A periphery of the annular shape first lens includes guide members configured to position the boss of the annular shape first lens to movably interact with the motion transfer member.
F21V 5/04 - Refractors for light sources of lens shape
F21V 17/00 - Fastening of component parts of lighting devices, e.g. shades, globes, refractors, reflectors, filters, screens, grids or protective cages
F21V 5/02 - Refractors for light sources of prismatic shape
A61B 90/30 - Devices for illuminating a surgical field, the devices having an interrelation with other surgical devices or with a surgical procedure
F21W 131/205 - Lighting for medical use for operating theatres
A surgical light head and proximity detection method includes a housing, a plurality of light emitting elements arranged in the housing and configured to direct light at a target region of interest, and a plurality of distance sensors arranged in the housing. At least two of the distance sensors have field of views that overlap to define a common detection region of interest and the common detection region of interest at least partially overlaps with the target region of interest. The light head may have a plurality of integrally formed tilted seats that position the distance sensors relative to a center line of focus of the surgical light head. The distance sensors may be integrated in the housing via an optical component that is sealed relative to the housing and covers the distance sensor while enabling transmission and receipt of distance sensing signals therethrough.
A light head for a medical device support system. The light head includes first and second zones of light sources, an optical system, and a control system. The first and second zones of light sources emit respective first and second beams of light that form an illumination pattern having a pattern size at a region of interest. The optical system adjusts a beam spread of the second beam of light to change the pattern size of the illumination pattern from a first pattern size to a second pattern size. The control system varies power to the first and second zones of light sources in response to adjustment of the beam spread of the second beam of light to maintain a substantially constant magnitude of illuminance at the region of interest as the pattern size is changed from the first pattern size to the second pattern size.
F21V 5/04 - Refractors for light sources of lens shape
F21V 14/06 - Controlling the distribution of the light emitted by adjustment of elements by movement of refractors
F21V 23/00 - Arrangement of electric circuit elements in or on lighting devices
A61B 90/00 - Instruments, implements or accessories specially adapted for surgery or diagnosis and not covered by any of the groups , e.g. for luxation treatment or for protecting wound edges
H05B 45/00 - Circuit arrangements for operating light-emitting diodes [LED]
A lighting assembly includes a light transmissive substrate extending along a length and including a light emission portion including opposed first and second major surfaces spaced apart from one another in a thickness direction, an inner edge surface extending between the first and second major surfaces in the thickness direction, and an outer edge surface opposed the inner edge surface and extending in the thickness direction. An extension portion extends from the light emission portion proximate the second major surface in the thickness direction. A light source is attached to the extension portion. A light head includes a housing, a primary light source attached to the housing, and the lighting assembly as an auxiliary lighting assembly. The housing includes a channel in which the auxiliary lighting assembly is retained.
F21V 5/04 - Refractors for light sources of lens shape
F21S 8/06 - Lighting devices intended for fixed installation intended only for mounting on a ceiling or like overhead structure by suspension
F21V 21/28 - Pivoted arms adjustable in more than one plane
F21Y 105/18 - Planar light sources comprising a two-dimensional array of point-like light-generating elements characterised by the overall shape of the two-dimensional array polygonal other than square or rectangular, e.g. for spotlights or for generating an axially symmetrical light beam
A heating element includes an electrically insulating layer; resistive layer formed of a positive temperature coefficient material; and an electrically conductive layer disposed between the electrically insulating layer and the resistive layer and including a first bus and a second bus that is spaced apart from the first bus, the resistive layer electrically connecting the first bus and the second bus. The electrically insulating layer, the electrically conductive layer, and the resistive layer are stacked to form a lamination and the lamination having a thickness and a width and length extending orthogonal to the thickness. The lamination may have slits extending through the thickness thereof and along a portion of the length thereof. Terminals may be connected to the buses and arranged to provide a counter current flow pattern across the lamination. The lamination may be used in a warming device and in connection with a patient warming system.
H05B 3/14 - Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor characterised by the composition or nature of the conductive material the material being non-metallic
H05B 3/16 - Heating elements characterised by the composition or nature of the materials or by the arrangement of the conductor the conductor being mounted on an insulating base
H05B 3/34 - Heating elements having extended surface area substantially in a two-dimensional plane, e.g. plate-heater flexible, e.g. heating nets or webs
A patient warming system includes a control unit coupled to one or more warming devices. The control unit may control application of power to the heating elements of the warming devices. The control unit may provide hardware and/or software approaches to monitor and detect an overtemperature situation and/or fault of a given warming device.
A61F 7/00 - Heating or cooling appliances for medical or therapeutic treatment of the human body
G16H 40/63 - ICT specially adapted for the management or administration of healthcare resources or facilities; ICT specially adapted for the management or operation of medical equipment or devices for the operation of medical equipment or devices for local operation
G16H 20/30 - ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to physical therapies or activities, e.g. physiotherapy, acupressure or exercising
98.
SURGICAL LIGHT HEAD WITH BEAM SPREADING AND ADJUSTABLE POWER BALANCING
A light head for a medical device support system. The light head includes first and second zones of light sources, an optical system, and a control system. The first and second zones of light sources emit respective first and second beams of light that form an illumination pattern having a pattern size at a region of interest. The optical system adjusts a beam spread of the second beam of light to change the pattern size of the illumination pattern from a first pattern size to a second pattern size. The control system varies power to the first and second zones of light sources in response to adjustment of the beam spread of the second beam of light to maintain a substantially constant magnitude of illuminance at the region of interest as the pattern size is changed from the first pattern size to the second pattern size.
A lighting assembly (140) includes a light transmissive substrate (142) extending along a length and including a light emission portion including opposed first and second major surfaces spaced apart from one another in a thickness direction, an inner edge surface extending between the first and second major surfaces in the thickness direction, and an outer edge surface opposed the inner edge surface and extending in the thickness direction. An extension portion extends from the light emission portion proximate the second major surface in the thickness direction. A light source (156) is attached to the extension portion. A light head (100) includes a housing (116), a primary light source (123) attached to the housing (116), and the lighting assembly (140) as an auxiliary lighting assembly (140). The housing (116) includes a channel in which the auxiliary lighting assembly (140) is retained.
F21Y 105/18 - Planar light sources comprising a two-dimensional array of point-like light-generating elements characterised by the overall shape of the two-dimensional array polygonal other than square or rectangular, e.g. for spotlights or for generating an axially symmetrical light beam
F21Y 109/00 - Light sources with light-generating elements disposed on transparent or translucent supports or substrates
F21Y 113/20 - Combination of light sources of different form
A surgical light head and proximity detection method includes a housing, a plurality of light emitting elements arranged in the housing and configured to direct light at a target region of interest, and a plurality of distance sensors arranged in the housing. At least two of the distance sensors have field of views that overlap to define a common detection region of interest and the common detection region of interest at least partially overlaps with the target region of interest. The light head may have a plurality of integrally formed tilted seats that position the distance sensors relative to a center line of focus of the surgical light head. The distance sensors may be integrated in the housing via an optical component that is sealed relative to the housing and covers the distance sensor while enabling transmission and receipt of distance sensing signals therethrough.
