Abstract: Packaging systems and methods for wet storage and/or shipping of prosthetic heart valve or other medical devices are disclosed.

Abstract: A user equipment (UE) may monitor a channel for wireless communication associated with a first radio access technology (RAT) during one or more of a first active duration or a first inactive duration. The UE may operate in a first power mode during the first inactive duration. The UE may monitor the channel for wireless communication associated with a second RAT during one or more of a second active duration or a second inactive duration. The UE may operate during the second inactive duration in one or more of the first power mode or a second power. The UE may operate according to the first mode or the second mode based on the monitoring of the channel associated with the first RAT and the second RAT.

Abstract: A “dry” packaging in which a prosthetic heart valve is packaged within a container with hydrogel that can be provided in many forms. Certain embodiments include hydrogel that is preloaded with glycerol or the like. The hydrogel regulates the humidity within the container through a diffusion-driven mechanism if a gradient of humidity between the inside and the outside of the hydrogel exists. Humidity regulation is important to prevent the tissue of the valve structure from drying out. When the partially-hydrated hydrogel is present within container, which is saturated with air of a predefined humidity, the water molecules from the air will be absorbed by the hydrogel if the air humidity is high (i.e. when the thermodynamics favor hydrogel hydration) or vice versa. Various embodiments are configured to also house at least a portion of a delivery device for delivering the prosthetic heart valve.

Abstract: A magnetoelectric element of a surgical tool positioned in the body of a subject is controllably bent or elongated under the influence of an applied magnetic field. A piezoelectric layer in the magnetoelectric element provides output that can be used to determine the actual amount of bending or elongation of the magnetoelectric element, and this actual amount is compared to a theoretical amount of bending or elongation which would result from the applied magnetic field. Any differences between the actual and theoretical amounts provide feedback to the surgeon for performing the surgical procedure. Preferably, tactile feedback is provided to the surgeon.

Abstract: A magnetoelectric element of a surgical tool positioned in the body of a subject is controllably bent or elongated under the influence of an applied magnetic field. A piezoelectric layer in the magnetoelectric element provides output that can be used to determine the actual amount of bending or elongation of the magnetoelectric element, and this actual amount is compared to a theoretical amount of bending or elongation which would result from the applied magnetic field. Any differences between the actual and theoretical amounts provide feedback to the surgeon for performing the surgical procedure. Preferably, tactile feedback is provided to the surgeon.