A thrombus detection device comprising an elongate tube having at least one opening at a distal end of the elongate tube. A coupling is attached or formed at the proximal end of the elongate tube. The detection of the presence of a thrombus is performed by using a syringe to withdraw blood through the at least one thrombus detection opening at the distal end of the elongate tube. If little or no blood is withdrawn, or if the withdrawal of blood is more difficult than expected, the presence of a thrombus obstructing the openings is indicated.

Apparatus for delivery of bone includes a syringe body and a plunger. The syringe body includes a tip at a bottom thereof, a funnel-shaped top at the top thereof, and a tubular section having a generally cylindrical interior wall defining a passageway extending from the funnel-shaped top to the tip. The plunger includes an elongate piston, a press head, and a handle. The piston extends between the press head at a lower end of the plunger, and the handle at an upper end of the plunger. The plunger is removably received within the passageway, with an extent of the plunger extending out of the funnel-shaped top away from the syringe body. The syringe body may be loaded with one or more bone pellets or cartridges containing bone.

Inflation systems and methods for inflating a balloon member are provided. The inflation system includes an inflation tool. The inflation tool includes a first component having a first arm where the first arm extends longitudinally along an axis of movement of the first component. The first arm includes a first and a second positioning member, the first positioning member is longitudinally spaced apart from the second positioning member. The first component is adapted to advance distally for inflation of the balloon member. Each positioning member corresponds to an inflation increment for the balloon member.

A device for estimating breast implant volume is provided, which may include an input interface and a processing circuit. A numerical value may be inputted in to the input interface. The processing circuit may calculate the estimation value of breast implant volume according to a linear model and the numerical value. The processing circuit may multiply the numerical value by a coefficient to generate a product, and add a constant to the product to generate the estimation value of breast implant volume, wherein the numerical value may be a breast sample weight or a breast size.

Pulsatile balloon catheter systems are provided. Aspects of the systems include: a pulse generator; and a balloon catheter assembly operably connected to the pulse generator. In embodiments, the balloon catheter assembly includes: a proximal connector operably connecting the balloon catheter assembly to the pulse generator and configured to transduce a first pulse energy generated by the pulse generator to a second pulse energy; a distal balloon; and a catheter component, where the catheter component includes a fluidic passage operably positioned between the proximal connector and the distal balloon, which passage is configured to propagate the second pulse energy from the proximal connector along the fluid passage to the distal balloon. Also provided are balloon catheter assemblies and kits that include the same. Also provided are systems and methods for assessing vessel compliance in-vivo. Also provided are systems and methods for determining system state of balloon catheter systems. The systems, assemblies and kits find use in a variety of different applications, including balloon angioplasty applications.

A tourniquet for occluding blood flow to a limb is improved by the addition of proximal and distal strain gauges. The proximal strain gauge may be monitored under conditions of total blood flow occlusion for time-varying signals indicative of volumetric limb changes arising from the subject's blood flow in the proximal section of the limb. Upon a change in limb occlusion pressure, the signals from the proximal strain gauge can be observed to change also, and the working pressure in the tourniquet can be adjusted safely in response. Automated control systems may further use inputs from a distal strain gauge and/or from a sensor that detects induced pressure changes within the tourniquet to improve the control of the tourniquet working pressure during operation to avoid unwanted blood flow past the tourniquet.

A system includes an injection device that is configured to be fluidly coupled to the catheter and a sensing device that is configured to sense an injected volume of fluid in the inflatable balloon of the catheter. A controller is coupled by a wired or wireless communication link to the sensing device to receive an injected volume signal from the sensing device. The controller is configured to determine an actuation pressure based on the injected volume of the fluid in the inflatable balloon. A pressure relief valve is fluidly coupled to the catheter and coupled by a wired or wireless communication link to the controller. The controller is configured to adjust the actuation pressure of the pressure relief valve based on the injected volume of the fluid in the inflatable balloon.

A parturition drape (100) includes a drape (101) and a twin pouch assembly (102). The twin pouch assembly defines a first pouch (1101) and a second pouch (1301) attached to a major face of the drape. A flap (103) is attached to the major face of the drape. The flap (103) is selectively insertable into an open end of either the first pouch or the second pouch.

A catheter devices/systems and methods therefrom are described herein for treating acute kidney injury, especially the contrast-induced acute kidney injury wherein the devices prevent the contrast dyes from entering into kidney and/or facilitate blood flow of kidney by said catheter system.

A grasping instrument for clamping tissue includes an outer tube, first and second jaw members supported by the outer tube, a carriage mounted within the outer tube and configured for longitudinal movement between an initial proximal position and an advanced distal position to cause corresponding movement of the first and second jaw members between an approximated condition and an open condition, a piston operatively coupled to the carriage, an inflatable membrane disposed within the piston and being selectively inflatable to a predefined internal pressure to cause corresponding distal longitudinal movement of the piston a predetermined distance and to cause proximal longitudinal movement of the carriage to apply a clamping force to the tissue disposed within the first and second jaw members and an indicator bar having visual indicators corresponding to various degrees of thickness of the tissue disposed within the first and second jaw members.