Provided is a biological information detection device capable of restraining noise from being mixed with a signal relating to biological information. A biological information detection device includes an electrode pad that is able to detect a signal (bioelectric signal) relating to biological information of a subject (for example, a fetus in a mother's body), a connector that is connectable to the electrode pad, and a cable that is connected to the connector and is able to transmit the signal. The electrode pad and the connector are provided with fixing members and that are attachable to and detachable from each other, respectively.

An electrode device for aEEG is disclosed. The electrode device includes a housing mounted on an adhesive element to adhere the electrode device to a skin surface of a patient; an electrode plate placed in the housing; and a wire connection for the electrode plate. The housing has a first protruding part that includes a conical-shaped hole for injecting and removing an electroconductive gel and that is disposed in the housing inclined outwardly at an angle between 50 degree and 80 degree with respect to the longitudinal direction of the skin surface. The housing also has a second protruding part that includes a hole for the introduction of the wire connection in order to be attached to the electrode plate. The second protruding part is disposed on the axis of the housing

An electrode device for aEEG is disclosed. The electrode device includes a housing mounted on an adhesive element to adhere the electrode device to a skin surface of a patient; an electrode plate placed in the housing; and a wire connection for the electrode plate. The housing has a first protruding part that includes a conical-shaped hole for injecting and removing an electroconductive gel and that is disposed in the housing inclined outwardly at an angle between 50 degree and 80 degree with respect to the longitudinal direction of the skin surface. The housing also has a second protruding part that includes a hole for the introduction of the wire connection in order to be attached to the electrode plate. The second protruding part is disposed on the axis of the housing

A first layer (301) has an outer surface (302) facing away from the wearer and an inner surface (304) facing towards the wearer. The first layer (301) comprises a recess (303a, 303b). A sensing component (100a, 100b) is attached to he inner surface (304) and comprises fabric base component (101) and first and second conductive regions (109a, 109b, 111a, 111b). The base component (101) has an outer surface (105) facing the inner surface (304) and an inner surface (103) facing towards the wearer. The first conductive region (109a, 109b) is provided on the inner surface (103) and forms an electrode. The second conductive region (111a, 111b) is provided on the outer surface (105). The second conductive region (111a, 111b) is aligned with the recess (303a, 303b) in the first layer of material (301) and forms a connection terminal for connecting with an interface element of an electronics module (200).

The present disclosure provides a system that includes an arrangement of body surface electrodes on one or more patches adapted to be placed an outer surface of a patient's body. A computing apparatus includes non-transitory memory to store data and instructions executable by a processor thereof. The data includes anatomical geometry data, electrode geometry data and electrical data. The instructions can be programmed to register the anatomical geometry data and the electrode geometry data to provide co-registered geometry data representing the anatomy of the patient and the locations of the body surface electrodes in a common three-dimensional space. Electrophysiological signals can be reconstructed on a cardiac envelope of the heart based on the co-registered geometry data and the electrical data.

A biosensor having a satisfactory wearing comfort is provided, taking the compressive elastic modulus, the thickness and the planar area of the component into account. The biosensor includes a substrate having a rigidity K of 3.0 N.Math.mm.sup.2 or less expressed by following formula (1), and a component provided on a first main surface of the substrate, the component having a rigidity that satisfies following formula (2) and is equal to or greater than a predetermined value,
K=ET.sup.3/12  (1)
K≤6.34×10.sup.14×S.sup.−10.6  (2)
where E and T in formula (1) denote a compressive elastic modulus at 23° C. expressed in megapascals (MPa), and a thickness expressed in millimeters (mm), respectively. In formula (2), K denotes the rigidity expressed by formula (1) in newton millimeters squared (N.Math.mm.sup.2), and S denotes a planar area expressed in square centimeters (cm.sup.2).

A biosensor having a satisfactory wearing comfort is provided, taking the compressive elastic modulus, the thickness and the planar area of the component into account. The biosensor includes a substrate having a rigidity K of 3.0 N.Math.mm.sup.2 or less expressed by following formula (1), and a component provided on a first main surface of the substrate, the component having a rigidity that satisfies following formula (2) and is equal to or greater than a predetermined value,
K=ET.sup.3/12  (1)
K≤6.34×10.sup.14×S.sup.−10.6  (2)
where E and T in formula (1) denote a compressive elastic modulus at 23° C. expressed in megapascals (MPa), and a thickness expressed in millimeters (mm), respectively. In formula (2), K denotes the rigidity expressed by formula (1) in newton millimeters squared (N.Math.mm.sup.2), and S denotes a planar area expressed in square centimeters (cm.sup.2).

A living body sensor includes a flexible substrate including a body section; a first pad section, at one longitudinal directional end of the body section via a first constricted section, including a first electrode to be attached to a living body; a second pad section, at another longitudinal directional end of the body section via a second constricted section, including a second electrode to be attached to the living body; an obtaining section for obtaining biological information through the first second electrodes; a wireless communication section for transmitting the biological information; a component mounting section at the first constricted section side of the body section; and a battery setting section at the second constricted section side of the body section for setting a battery supplying power to the component mounting section. These sections are formed integrally with the flexible substrate.

The present invention relates to a stimulation electrode comprising an ionically conductive pressure sensitive adhesive composition comprising a) a (meth)acrylate resin comprising at least 10% of a (meth)acrylate monomer comprising OH-group by weight of the total weight of the (meth)acrylate resin; and b) an ionic liquid. The stimulation electrode according to the present invention is used in skin applications transferring an electrical signal to the body via skin.

The present invention relates to a stimulation electrode comprising an ionically conductive pressure sensitive adhesive composition comprising a) a (meth)acrylate resin comprising at least 10% of a (meth)acrylate monomer comprising OH-group by weight of the total weight of the (meth)acrylate resin; and b) an ionic liquid. The stimulation electrode according to the present invention is used in skin applications transferring an electrical signal to the body via skin.