A disposable, multiple layer surgical drape is provided. The surgical drape includes a bottom layer configured as a fluid impervious layer, a middle layer configured as a fluid absorbent layer, and a top layer configured as a fluid repellent layer. The middle layer is disposed between the top and bottom layers and has varying thickness. The top layer includes one or more continuity breaks exposing the middle layer.

A medical instrument comprises an instrument control surface configured to mate with an instrument sterile adapter to receive input drive forces through the sterile adapter to control actuation of the surgical instrument, the instrument control surface comprising a first opening defined in the instrument control surface. A latch structure of the instrument comprises a locking surface configured to engage a latch arm in response to the latch arm being received in the opening, wherein in an engaged state of the latch arm with the locking surface the medical instrument is attached to the instrument sterile adapter and the latch structure prevents movement of the latch arm in a first direction. A latch release is moveable in the engaged state of the latch arm with the locking surface to exert a force causing movement of the latch arm in a second direction to disengage the latch arm from the locking surface.

An antiseptic solution including, a cationic antiseptic agent, a film forming polymer, an anionic tinting agent, and a solvent, wherein the cationic antiseptic agent, the film forming polymer and the anionic tinting agent each remain solubilized within the solution for greater than about 1 hour at 25° C. and 60% relative humidity. The antiseptic agent is preferably octenidine dihydrochloride or chlorhexadine gluconate. The film forming polymer is preferably an acrylate polymer. The solvent is preferably ethanol, isopropanol, and n-propanol. When a drape is adhered to a dried surgical film via the antiseptic solution, the force required to peel the drape from the surgical film is at least about 105 g/25 mm.

A surgical drape is configured for covering a patient and an ultrasonography probe during surgical treatment of the patient. The surgical drape may include a first portion that includes a canopy portion. The canopy portion can be sized and shaped to at least partially cover a mechanical arm coupled to the ultrasonography probe and a proximal portion of the ultrasonography probe, and the canopy portion can be configured to move with the proximal portion of the ultrasonography probe when the ultrasonography probe is supported by the mechanical arm. A second portion can be coupled to the first portion, in which the second portion is sized and shaped to cover at least a portion of a torso of the patient.

A surgical system includes a light source, a sensor for detecting light, and a surgical device including an elongate shaft having a distal part positionable at a surgical working site within a body cavity. A first optical pathway transmits light from the light source to a distal part of the elongate shaft and onto tissue within the body cavity, and a second optical pathway receives light from tissue within the body cavity and transmits the received light to the sensor. A surgical drape, such as one covering a robotic manipulator arm housing components of the system, is positioned such that at least the first or second optical pathway includes an optically transmissive portion of the surgical drape.

Melt-blown webs having no shots and improved barrier properties, whereby the melt-blown webs are made out of a so-called “controlled rheology” propylene (CR-PP), which was visbroken without any peroxide.

A spunbond nonwoven fabric, comprising fibers of a propylene-based polymer composition containing 100 parts by mass of a propylene-based polymer (A) and 1 part by mass to 10 parts by mass of an ethylene-based polymer (B) having a density of from 0.93 g/cm.sup.3 to 0.98 g/cm.sup.3, wherein air permeability measured in accordance with JIS L 1096 (2010) by a Frazier type air permeability tester at a flow rate corresponding to a pressure differential of 125 Pa is 500 cm.sup.3/cm.sup.2/s or less.

A medical drape which is positioned over the head and upper torso of a patient is disclosed which includes a head flap, a head portion, a torso portion, and two oppositely disposed arm portions. The head flap is of a sufficient length to extend about the backside of the patient=s head. The head portion includes oppositely disposed side wings which aid in covering the head of a patient. Each arm portion includes an access slot extending through the arm portion.

Products and methods for producing products which comprise polyethylene and inorganic minerals for a single layer plastic composition.

Compositions and methods for inhibiting and interrupting biofilm formation, and for destabilizing established biofilms are provided, the novel compositions including polymeric resins and monomeric non-polymerizable and polymerizable resins. More particularly, the compositions and methods enable the protection and removal of biofilms from surfaces in the context of medical, consumer, domestic, food service, environmental and industrial applications, where the effects constitute beneficial and desirable biofilm attenuating activity.