By providing a surface light source that planarly emits first illuminating light FL in the blue wavelength region of 400 to 500 nm and second illuminating light SL in the red wavelength region of 600 to 660 nm, and by emitting illuminating light in these specific wavelength region, it makes it possible to visually identify the position of veins easily.

An arrangement for producing a sample of body fluid from a wound opening created in a skin surface at a sampling site includes: a housing, the housing comprising a first opening; a skin interface member disposed in the first opening, the skin interface member comprising an inner member having a second opening, and an outer member at least partially surrounding the inner member and attached to the first opening; and at least one skin-penetration member configured and arranged to project within the second opening. Arrangements having alternatively constructed skin interface members are also described.

The invention relates to the field of integrated systems which comprise a test element and a lancet which can be firstly used to make a wound in a skin opening in order to collect a sample. The sample is subsequently directly taken up by the test element in the process of which it comes into contact with a reagent contained in the test element and results in an optically detectable change in a test field. The change in the test field is detected by means of an analytical unit which is optically contacted with the test field via at least one light-conducting element.

A specimen collection assembly including a flow control member for adjustably altering a flow path is disclosed. In one configuration, the flow control member defines a regulation channel in fluid communication with a lumen of a cannula, wherein the flow control member is configured to adjustably alter an effective flow distance between the lumen of the cannula and an interior of an evacuated collection container. In another configuration, the flow control member is positioned to vary an effective cross-sectional area of at least one of an inlet port and an outlet port adapted to be in fluid communication with the lumen and the evacuated collection container.

Sample processing methods and systems to collect a biological sample. A device may be configured collect a predetermined volume of a sample in sample chamber, and seal the chamber upon activation. The device may be further configured to mix the mix the sample with a predetermined volume of a reagent and/or mix the sample and the reagent in a pre-determined ration.

Bodily fluid sample collection systems, devices, and method are provided. The sample is collected at a first location and subjected to a first sample processing step. The sample may be shipped to a second location and subjected to a second sample processing step that does not introduce contaminants into a plasma portion of the sample formed from the first processing step. The sample may also be mixed with other material(s) in the collection device.

The present invention generally relates to systems and methods for monitoring and/or providing feedback for drugs or other pharmaceuticals taken by a subject. In one aspect, the present invention is directed to devices and methods for determining a species within the skin of a subject; and producing feedback to a subject based on the determination of the species. The feedback may be, for example, visual, audible, tactile, a change in temperature, etc. In some cases, information regarding the determination of the species may be transmitted to another entity, e.g., a health care provider, a computer, a relative, etc., which may then provide feedback to the subject in some fashion. In some cases, the feedback may be directly indicative of the species. However, the feedback may also be indirect in some embodiments.

A data processing system is configured to identify treatment responsive to a health risk determined from feature data provided by one or more networked data sources. A classification engine generates a feature vector based on a natural language processing (NLP) of input data representing words provided by a user. Features of the feature vector represent health risk factors. Machine learning logic classifies the features to generate a classification metric indicating whether the features are indicative of health risks or not indicative of health risks. A prediction value is generated indicating a likelihood of each health risk factor for the patient. The patient can be diagnosed with a health condition or disease based on the identified health risks.

A method and system for providing interactive wellness recommendations is disclosed. The system stores information regarding health profiles, each profile comprised of health data. An individual user health profile can be associated with at least one cohort group. The system obtains individual user health data to develop a user health profile and assigns the user to at least one cohort group based on the user health profile. The system also obtains a user wellness goal. Using the user health profile, a recommendation engine generates a user wellness recommendation for obtaining the user wellness goal based on the user's membership in at least one cohort group by correlating the particular health profile against effective wellness regimens for the user wellness goal as it relates to the cohort group. The user wellness recommendation may then be provided to the user. The user may be continually monitored through any number of methods. As new user health data is obtained, the system can monitor user progress towards their wellness goal and revise the user wellness recommendation based on that progress.

A finger receptacle having an elongated, flexible sleeve having a length defined between a proximal end and a distal end, the sleeve further comprising a support base, a ceiling and a top surface defining a longitudinal axis X, whereby the sleeve is adapted to bias toward a radially contracted state and when urged into a radially expanded state effects a radial compression action about the length to releasably secure a finger within the receptacle; and at least one angled projection extending from the ceiling and top surface at the distal end of the sleeve, the at least one angled projection angled inwardly from the longitudinal axis X of the ceiling and adapted to contact a nail of the finger releasably secured in the sleeve at the distal end of the receptacle to effect a second compression action. The invention further related to devices of blood capture and blood collection and those that incorporate said receptacle or a finger compression sleeve.