A method of applying pressure and support to a patient's abdomen during an endoscopy procedure including applying a primary wrap comprising a band of elastic material to an abdomen of a patient and maintaining tension in the band in order to apply constant pressure and the support to the patient's abdomen through a contraction of the primary wrap in connection with an advancement or a withdrawal of an endoscope during an enteroscopy procedure. The method includes adjusting at least one of the primary wrap or at least one secondary strap extending from the primary wrap to adjust compression and support the advancement or the withdrawal of the endoscope through the contraction of the primary wrap and the at least one secondary strap.

A sterile bag for covering medical equipment comprises: a barrier section, a flexible body section, and an attaching section. The flexible body section has a tubular shape extending from a proximal end to a distal end thereof, and an outer surface, an inner surface, and an open end. The barrier section is coupled to the proximal end, and the attaching section is formed at the distal end of the flexible body section. The barrier section is a rigid or semirigid component which attaches the sterile bag to a sterile component or to an unsterile component of the medical equipment in a pleaded or folded state. The flexible body section is configured to be deployed over the unsterile component so as to enclose within the inner surface thereof the unsterile component. The unsterile component is connectable to the sterile component through the central opening of the barrier section.

An apparatus for holding a medical device includes: a device sheet perpendicular to the ground; and at least one pocket layer, including a first pocket layer, where the first pocket layer is configured as a single first pocket room in its entirety and has a length enabling the medical device to be laid in the first pocket room without coiling in the presence or absence of one or more suspension elements, and the at least one pocket layer has a structure in which an edge of the at least one pocket layer facing the one or more suspension elements is open and other edges thereof are peripherally attached to the device sheet.

A sterile bag for covering medical equipment comprises: a barrier section, a flexible body section, and an attaching section. The flexible body section has a tubular shape extending from a proximal end to a distal end thereof, and an outer surface, an inner surface, and an open end. The barrier section is coupled to the proximal end, and the attaching section is formed at the distal end of the flexible body section. The barrier section is a rigid or semirigid component which attaches the sterile bag to a sterile component or to an unsterile component of the medical equipment in a pleaded or folded state. The flexible body section is configured to be deployed over the unsterile component so as to enclose within the inner surface thereof the unsterile component. The unsterile component is connectable to the sterile component through the central opening of the barrier section.

Connection systems are disclosed for establishing one or more electrical connections through a drape. An example connection system includes a first connector and a second connector configured to connect to each other. The first connector includes a first-connector housing, an electrical lead extending from the first-connector housing, and at least a first piercing element within the first-connector housing configured to pierce the drape. The first piercing element is orthogonally connected to the electrical lead. The second connector includes a second-connector housing and at least a first receptacle within the second-connector housing. The first receptacle is configured to form at least a first electrical connection of the one or more electrical connections with the first piercing element when the first connector is disposed over the second connector with the drape therebetween. Methods are also disclosed herein for establishing one or more electrical connections through a drape with the connection systems.

An apparatus includes a pad assembly, an injector assembly, an injector driver, and a fluid source. The pad assembly is sized and configured to be placed on a forehead of a patient. The injector assembly includes a body, a flexible cannula, and a needle. The body is configured to be removably secured to the pad assembly. The cannula is sized to be inserted through an incision in an eye of a patient. The needle is slidably disposed in the cannula. The injector driver is operable to drive the needle longitudinally relative to the flexible cannula. The fluid source assembly is in fluid communication with the needle.

Apparatus for optical imaging of Cerenkov luminescence from an object subsequent to the object receiving a dose of a radiopharmaceutical, the apparatus comprising: a light tight enclosure within which the object can be received at a sample location; an imaging means; a means to mitigate direct particle impingement between the sample location and the imaging means; and one or more optical elements for transmitting Cerenkov photons from within the light tight enclosure to the imaging means.

A surgical drape includes a center section having an operating window and extending longitudinally from a head end to a foot end, and a side section positioned on each longitudinal side of the center section. The side sections may be at least partially transparent. An elastic band extends through outermost ends of the side sections and across the foot end of the center section, and at least one surgical fluid collection pocket is disposed adjacent the operating window. Additional features of the drape may include a warming bladder and/or an extension section that is expandable to cover a machine adjacent the drape, such as an x-ray fluoroscope machine.

A system and/or method for isolating respiratory excretions from a patient during a medical procedure performed on the airways of a patient. A shield device includes a barrier, one or more support arms, and an access port. The barrier can be a flexible material, and is impervious to air. The support arm(s) maintain the barrier in a deployed state for placement over a patient's head, including the patient's mouth and nose being located within an isolation region established by the barrier. The access port is carried by the barrier and is configured to permit sealed passage of a medical device (e.g., an endoscope) into the isolation region for interfacing with the patient's airway.

Connection systems and methods for establishing optical and electrical connections through a drape are disclosed. A connection system can include a plug and a receptacle, the plug being configured to insert into the receptacle with the drape therebetween. The plug can include an optical terminal extending from a plug housing and an electrical terminal extending from the plug housing. The electrical terminal can be configured as a piercing element for piercing the drape. The receptacle can include an optical receiver within a receptacle housing and an electrical receiver within the receptacle housing. The optical receiver can be configured to form the optical connection with the optical terminal, and the electrical receiver can be configured to form the electrical connection with the electrical terminal when the plug is inserted into the receptacle with the drape therebetween.