Abstract: A hydrogel pad is configured for use with an electrode or a wearable device to measure vital signs of a patient. The hydrogel pad includes a flexible support having one or more openings in which hydrogel is disposed. A membrane covers one side of the hydrogel to protect it from gaining or losing too much moisture. A removable backing covers the other side of the hydrogel until it is applied to a patient, at which point the other side contacts the patient's skin. The protective membrane can be pierced by an angular conductive contact of a device to contact the hydrogel creating an electric conduit between the patient and the device. When the device is removed, the membrane at least partially closes to cover and protect the hydrogel.

Abstract: A hydrogel pad is configured for use with an electrode or a wearable device to measure vital signs of a patient. The hydrogel pad includes a flexible support having one or more openings in which hydrogel is disposed. A membrane covers one side of the hydrogel to protect it from gaining or losing too much moisture. A removable backing covers the other side of the hydrogel until it is applied to a patient, at which point the other side contacts the patient's skin. The protective membrane can be pierced by an angular conductive contact of a device to contact the hydrogel creating an electric conduit between the patient and the device. When the device is removed, the membrane at least partially closes to cover and protect the hydrogel.

Abstract: A hydrogel pad is configured for use with an electrode or a wearable device to measure vital signs of a patient. The hydrogel pad includes a flexible support having one or more openings in which hydrogel is disposed. A membrane covers one side of the hydrogel to protect it from gaining or losing too much moisture. A removable backing covers the other side of the hydrogel until it is applied to a patient, at which point the other side contacts the patient's skin. The protective membrane can be pierced by an angular conductive contact of a device to contact the hydrogel creating an electric conduit between the patient and the device. When the device is removed, the membrane at least partially closes to cover and protect the hydrogel.

Abstract: A cuff system includes a flexible substantially tubular sheath having a distal end, a proximal end, a central longitudinal axis, and a central channel extending along the longitudinal axis. The system also includes a first guide disposed at the proximal end of the sheath. The first guide is configured to control insertion of a cuff connector into the central channel in a first direction substantially parallel to the longitudinal axis. The system further includes an orifice proximate the distal end of the sheath. The orifice is configured to enable fluid connection between a portion of the cuff connector and an inflatable cuff while a remainder of the cuff connector is disposed within the central channel.

Abstract: A portable medical diagnostic instrument includes an instrument head and a handle portion having an open-ended receiving cavity. A compact illuminator defined by a housing retaining a miniature light source and a power supply is releasably fitted within the open-ended receiving cavity of the handle portion wherein the light source of the illuminator is optically coupled with the instrument on assembly therewith. The handle portion can be integral with the instrument or releasably attached. The handle portion according to at least one version is made from a plastic or other suitable material, permitting disposability and/or single patient use. In one version, the handle portion is flexibly deformable, at least partially, to facilitate release of the portable illuminator.

Abstract: A portable medical diagnostic instrument includes an instrument head and a handle portion having an open-ended receiving cavity. A compact illuminator defined by a housing retaining a miniature light source and a power supply is releasably fitted within the open-ended receiving cavity of the handle portion wherein the light source of the illuminator is optically coupled with the instrument on assembly therewith. The handle portion can be integral with the instrument or releasably attached. The handle portion according to at least one version is made from a plastic or other suitable material, permitting disposability and/or single patient use. In one version, the handle portion is flexibly deformable, at least partially, to facilitate release of the portable illuminator.

Abstract: Adaptive attachments used in combination with a blood pressure cuff enable various blood pressure measurements to be taken in a hospital or other setting having various single and/or dual lumen manual or electronic blood pressure measuring equipment with a single, patient-worn cuff.

Abstract: Adaptive attachments used in combination with a blood pressure cuff enable various blood pressure measurements to be taken in a hospital or other setting having various single and/or dual lumen manual or electronic blood pressure measuring equipment with a single patient-worn cuff.

Abstract: A medical workstation is defined by a supporting structure having at least one medical diagnostic instrument disposed thereupon. A first display is further disposed on a first side of the supporting structure and a second display is disposed on a second side of the supporting structure in a manner substantially opposite from the first display. Each of the first and second displays are interconnected to the at least one medical diagnostic instrument to permit at least one of the displays in order to display diagnostic results and are tandemly or independently controllable.

Abstract: A thermometry apparatus includes a housing that receives a probe having at least one temperature responsive element within an isolation chamber that is preferably removable from the housing. A switch assembly determines the presence of the isolation chamber in the housing wherein the apparatus is enabled only if the isolation chamber is attached to the housing and a probe is removed from the attached isolation chamber.

Abstract: The invention is in one embodiment an apparatus and a method for measuring the blood pressure of a vertebrate subject. The apparatus uses an inflatable chamber with a sensor to detect signals indicative of a blood pressure of the subject during an inflation interval of the inflatable chamber. If secondary motion or artifact signals are detected, the apparatus and method determine whether the secondary signals are below a predetermined value, and if so, complete the measurement. If the signals indicate that the measurement is not accurate, the system and method immediately institute a measurement of the blood pressure during a deflation interval, which can include a step deflation interval. In the event that the subject is identified as a neonate, the system and method immediately measure using the deflation interval procedure.