Abstract: A device for obtaining at least one physiological parameter of an individual, the device being a portable device comprising: body temperature measuring means (200) of the individual, display means configured to display the physiological parameter, the physiological parameter comprising the body temperature, communication means, for example with a communications network to which equipment is connected, in particular wireless, and processing means configured to transmit the physiological parameter to the equipment via the network.

Abstract: An assembly structured to aspirate nasal cavity of individuals including, but not limited to, children. A hand held and hand operative casing includes a negative pressure source preferably battery operated, and a cover assembly removably connected to the casing and structured to at least partially define a receiving chamber. An inlet assembly is formed in the casing and communicates with the negative pressure source at least partially by means of a path of fluid flow. A container is removably disposed within the receiving chamber in a predetermined, operative orientation sufficient to receive and collect a predetermined portion or phase of the aspirated fluid, such as mucus is removed from the nasal cavity. The path of fluid flow is disposed, dimensioned and structured to restrict passage of the heavier, predetermined portion or phase of the aspirated fluid thereby facilitating its collection within the container, which is disposable along with the collected aspirated fluid after use.

Abstract: An assembly structured to collect medical data from at least one but more practically a plurality of patients, wherein the medical data collected includes, but is not limited to, temperature readings. A hand-held device or housing is disposable in an operative position in spaced relation to a predetermined target of the patient. A sensor assembly is operative to collect the intended medical data and a memory assembly serves to concurrently store the collected data. A display assembly is operatively associated with a control assembly wherein the collected medical data from any one of the plurality of patients may be selectively accessed, reviewed on the display assembly and be correlated with additional identification information corresponding to each of the plurality of patients from which the collected data originated.

Abstract: An assembly structured aspirate nasal cavity of individuals including, but not limited to, children. A hand held and operative casing includes a negative pressure source preferably battery operated, and a cover assembly removably connected to the casing and structured to at least partially define a receiving chamber. An inlet assembly is formed in the casing and communicates with the negative pressure source at least partially by means of a path of fluid flow. A container is removably disposed within the receiving chamber in a predetermined, operative orientation sufficient to receive and collect a predetermined portion of the aspirated fluid, such as mucus removed from the nasal cavity. The path of fluid flow is disposed, dimensioned and structured to restrict passage of the heavier, predetermined portion of the aspirated fluid thereby facilitating its collection within the container, which is disposable along with the collected aspirated fluid after use.

Abstract: An assembly structured aspirate nasal cavity of individuals including, but not limited to, children. A hand held and operative casing includes a negative pressure source preferably battery operated, and a cover assembly removably connected to the casing and structured to at least partially define a receiving chamber. An inlet assembly is formed in the casing and communicates with the negative pressure source at least partially by means of a path of fluid flow. A container is removably disposed within the receiving chamber in a predetermined, operative orientation sufficient to receive and collect a predetermined portion of the aspirated fluid, such as mucus removed from the nasal cavity. The path of fluid flow is disposed, dimensioned and structured to restrict passage of the heavier, predetermined portion of the aspirated fluid thereby facilitating its collection within the container, which is disposable along with the collected aspirated fluid after use.