The subject matter described herein provides non-invasive patch stripping methods for the collection of a skin sample. The patch stripping method includes applying and removing at least one adhesive patch, provided that a skin sample is adhered to the adhesive patch after removal. The at least one adhesive patch is supplied in an adhesive skin sample collection kit. Optionally, the adhesive skin sample collection kit further comprises a sample collector and/or instructions for use.

A biosignal measurement system comprises an adapter for a biosignal measurement device, and an external support structure separate from the adapter. The adapter comprises tool-less connectors, which are repeatedly connectable to and disconnectable from their counter connectors of the external support structure, and a device connector, which has an electrical connection with the tool-less connectors and which has a connection with the biosignal measurement device that the adapter carries. The external support structure comprises an electrode support structure with electrodes and tool-less counter connectors, the electrodes and the tool-less counter connectors having an electrical connection therebetween. The electrodes form an electrical contact with skin for receiving the biosignal. The counter connectors are in electrical contact with the connectors of the adapter for transferring the biosignal to the biosignal measurement device through the adapter.

A patch and sensor assembly has a biosensor housed in a reusable portion that connects to a mapping and localization system (MLS) via biosensor wires. A disposable portion has an electrode layer through which signals are transmitted to the MLS via ACL wires. The biosensor and ACL wires extend through a single cable exiting the reusable portion. The disposable portion includes an adhesive layer for adhering the electrode layer to a patient, on the electrode layer, and an engagement element for detachably receiving at least a portion of the housing of the reusable portion. The reusable portion includes a housing in which the biosensor has biosensor wires that exit the reusable portion. The housing is also adapted to carry and/or provide support to an ACL contact member responsive to the electrode layer of the disposable portion, and ACL wires that exit the reusable portion.

Examples described herein include sensor devices for measuring a parameter of a user. The sensor devices may include a reusable portion (e.g., a sensor). The sensor devices may include one or more weakened portions that may fracture on removal of a portion of the sensor device from the user. Fracturing the weakened portions may expose the reusable portion (e.g., the sensor). Accordingly, the reusable portion may be more readily observed and collected for reuse.

Provided is a waterproof device that is impervious to water and can also use an air cell as a power source. The waterproof device of the present disclosure is worn on the body and includes a circuit unit, a power source, and an exterior package that protects the circuit unit and the power source. At least a part of the exterior package is composed of a water-repellent air-permeable sheet. The water-repellent air-permeable sheet has a water pressure resistance of 12 kPa or more.

A biological signal detection device is capable of accurately and simply measuring biological signals and promotes daily health care. A body abutting-side cushioning member 10 formed of a three-dimensional knitted fabric is substantially circular in plan view. A base cushioning member 20 is also substantially circular in plan view. A square one tends to undergo deformation such as turning-up or folding of its edges around the corners when, for example, a person sits thereon. Such deformation tends to distort detection data. Moreover, the folding and the like give a feeling of something foreign. In contrast, a substantially circular one less undergoes such folding and the like.

An injection sensing device (ISD) (e.g., wearable patch) is paired with an external device (e.g., a medication delivery pen and/or smart phone, iPad, computer) via wireless link or wireline connection. The ISD senses fluctuations in local skin temperature during an injection and provides to the external device captured data from the sensor relating to medicine delivery to a patient to ensure complete delivery and minimize MDD misuse or malfunction or inaccuracies in dosing. The ISD or external device can use captured data and corresponding time stamps to determine flow informatics such as flow rate, total dose delivered, and dose completion status. An LED on the ISD indicates delivery in progress and/or delivery completion.

A monitoring and/or therapy apparatus can include a contact layer having a stretchable or substantially stretchable substrate, at least one strain sensor coupled with the contact layer, and electronic circuitry electronically coupled with the at least one strain sensor configured to determine an amount of an elongation of the at least one strain sensor based on a change in a resistance or capacitance of the at least one strain sensor. The at least one strain sensor can include a plurality of stretchable tracks positioned on the substrate, and can be configured such that the resistance of the at least one strain sensor increases as the contact layer is elongated and/ or curved. In some arrangements, the apparatus and/or the substrate can be attached to or adjacent to a user’s joint, and/or a wound, and can be configured to have reduced pressure applied to the space under the contact layer..

An apparatus for monitoring a sleep parameter of a user includes an adhesive pad configured to conform to a surface of the user and a flexible element coupled to the adhesive pad. The flexible element includes a conductive fabric, and exhibits a modified electrical property in response to an applied force. The apparatus also includes a power source electrically coupled to the flexible element, and an electrical circuit electrically coupled to the power source and the flexible conductive element. The electrical circuit is configured to detect, during use, a change in an electrical property of the flexible element.

The present embodiments relate generally to apparatuses, systems, and methods for deploying a medical device to skin of a host. The apparatuses, systems, and methods may be directed to removing a liner for a medical device so that the medical device may couple to the skin of the host. The medical device may comprise an on-skin wearable medical device.