An aspect of the disclosure is to provide a method and a hearing aid system comprising; a microphone unit configured to receive an acoustical input and provide an audio signal based on the acoustical input, and wherein the audio signal includes a sound pressure level; a storing unit including a normal hearing loudness model, a loudness scheme, a stimulation model and a coding parameter model; a sound output unit configured to stimulate auditory nerve fibers of a recipient of the hearing aid system based on audible stimulations; a processing unit configured to; extract a normal hearing loudness based on the sound pressure level and the normal hearing loudness model, and the normal hearing loudness model includes a plurality of normal hearing loudness as a function of a plurality of sound pressure levels; transform the normal hearing loudness to a secondary hearing loudness according to a loudness scheme; determine a stimulation level within a dynamic range of a recipient of the hearing aid system based on the secondary hearing loudness and the stimulation model, where the stimulation model includes a relation between a plurality of stimulation levels and a plurality of secondary hearing loudness; determine one or more stimulation coding parameters based on the coding parameter model, where the coding parameter model includes a relation between the determined stimulation level and the one or more stimulation coding parameters; and wherein the processing unit is configured to generate the audible stimulations based on the determined one or more stimulation coding parameters and provide the audible stimulations via the sound output unit to the auditory nerve fibers of the recipient of the hearing aid system such that the recipient perceives the secondary hearing loudness.

Systems and methods for improved control and performance of cochlear implants are disclosed. In an embodiment, the audio environment is sampled, and a neural network determines suggested filter setting for the cochlear implant. The process is repeated such that, as the user moves through various audio environments having differing noise levels, satisfactory performance of the cochlear implant is maintained for the user.

A cochlear implant includes a cochlear lead, a housing, an antenna, a stimulation processor operably connected to the antenna and to the cochlear lead, a first fixation element, a second fixation element with a different configuration than the first fixation element, and a connector configured to simultaneously connect the first and second fixation elements to the housing in such a manner that the first and second fixation elements are independently detachable from the housing.

Examples disclosed herein are relevant to testing capacitors to identify potentially faulty DC blocking capacitors in implantable stimulators. In an example, the test includes selecting an active electrode, a return electrode, and a reference electrode. Short duration monophasic stimulation is used to charge up the DC blocking capacitors of the active and return electrodes. The electrodes are subsequently disconnected from all other nodes except a discharge circuit (e.g., a star circuit) and the tissue. The reference electrode is used to measure the voltage of the DC blocking capacitor of the active electrode during the charging phase and the discharging phase (via the discharge circuit). The characteristics of one or more of the capacitors charging or discharging can be sensed and then analyzed to determine whether the one or more capacitors are functioning properly. Faulty capacitors can be identified by comparing actual and expected characteristics.

An apparatus includes a housing configured to be implanted in or on a recipient. The apparatus further includes circuitry within the housing, the circuitry including at least one storage device configured to store at least one secret. The circuitry is configured to generate, using the at least one secret, at least one code corresponding to the at least one secret and to transmit at least one stimulation signal to the recipient, the at least one stimulation signal indicative of the at least one code.

The present biological electrode includes a conductive fabric (2) formed of base fibers which are filled with a conductor and/or to which the conductor is adhered, a thin metallic wire (3) formed into a spiral shape and covered with the conductive fabric (2) from a side of a distal end in an axis direction, and a filling material (5) with which a gap between the conductive fabric (2) and the thin metallic wire (3) is filled and which supports the conductive fabric (2) and the thin metallic wire (3), and he conductor is electrically connected with the thin metallic wire (3).

A system includes a unit for capturing ECAP signals induced at electrodes of an electrode array in response to stimulation of a cochlea by applying auditory nerve stimulation signals to the electrodes; a memory unit for storing the captured ECAP signals and/or ECAP data derived from the captured ECAP signals; an electrode migration detection unit for detecting electrode migration relative to the cochlea by comparing presently captured ECAP signals and/or ECAP data derived from such presently captured ECAP signals to stored previously captured ECAP signals and/or ECAP data derived from such previously captured ECAP signals; and a unit for outputting an alarm signal in case that electrode migration is detected by the electrode migration detection unit.

Presented herein are techniques for monitoring the physical state of a stimulating assembly to, for example, detect the occurrence of an adverse event. More specifically, an elongate stimulating assembly comprising a plurality of longitudinally spaced contacts is at least partially implanted into a recipient. Electrical measurements are performed at one or more of the plurality of contacts and the electrical measurements are evaluated relative to one another to determine the physical state of the stimulating assembly.

Antibacterial coatings and methods of making the antibacterial coatings are described herein. A first branched polyethylenimine (BPEI) layer is formed and a first glyoxal layer is formed on a surface of the BPEI layer. The first BPEI layer and the first glyoxal layer are cured to form a crosslinked BPEI coating. The first BPEI layer can be modified with superhydrophobic moieties, superhydrophilic moieties, or negatively charged moieties to increase the antifouling characteristics of the coating. The first BPEI layer can be modified with contact-killing bactericidal moieties to increase the bactericidal characteristics of the coating.

A headpiece including a housing, a headpiece magnet carried by the housing, and a headpiece antenna carried by the housing.