A medical, dental, or veterinary device with a use indicator includes a proximal end and a distal end configured to interact with a human or animal subject, the distal end including a use indication portion, wherein the use indication portion includes a reactive agent to react with a foreign substance to exhibit a visible change in appearance of the reactive agent to indicate to a veterinary, dental, or medical professional that the device had been previously used and must be sterilized or disposed.

An integrated testing device and fluid module are disclosed, as well as a method of manufacture. Fluid module contains a reservoir containing a test fluid, and a control vessel. The reservoir discharges test fluid into the control vessel, which discharges the test fluid in a controlled way to a test component.

An all-in-one self test kit includes: a test tool having a reagent container adapted to store a diagnosis reagent therein and a diagnosis kit with a casing constituted of a first body and a second body and a diagnosis strip disposed inside the casing and having a sucking part for sucking the diagnosis reagent and a diagnosis part reacting to the diagnosis reagent sucked to the sucking part; a sub-body having a container insertion portion for inserting the reagent container thereinto and a kit insertion portion for inserting the diagnosis kit thereinto; a main body for inserting the sub-body thereinto; and a cap fastened and unfastened with an entrance of the main body to open and close the main body.

The invention is generally a nasal pharyngeal and oral swab that may be mass-produced via three-dimensional (3D) printing. To achieve the right materials for 3D printing the swabs, exemplary embodiments employ a set of materials that result in a rigid structure that has bendable properties (at least in the neck or stem region of the swab), but more rigid and bridle properties at a breakpoint of the swab. In exemplary embodiments, this may be achieved by constructing the device of a first photosensitive material that is generally soft and bendable when cured, and a second photosensitive material that is generally rigid and brittle when cured, wherein the soft bendable material comprises of about 70% to 90% of the photosensitive composition used to 3D print the swab, and the rigid and brittle material comprises of about 30% to 10% of the photosensitive composition used to 3D print the swab.

The invention relates to a biological fluid test device (1), in particular a saliva test device, the device comprising:—a sample collector (2) in the form of a membrane, —a means for checking whether the quantity is sufficient, the collector being configured to cause a biological fluid to migrate to the checking means, - a means for displaying, on the device, a test result for at least one desired substance, characterised in that the device (1) comprises, or is associated with, at least one means for removing the collector and storing it for second expert opinion purposes. The invention also relates to a corresponding kit and method.

An optical analysis of saliva or a fluid-saliva mixture is performed in order to check whether the saliva or fluid-saliva mixture contains blood, which allows for determining whether or not a person may suffer from gingivitis or another condition affecting gum health. Light received from a representative volume of fluid (23) containing saliva is detected and analyzed. The analysis involves determination of at least one measurement value of light received by a light-receiving unit (25) for only a single wavelength of the light, particularly a wavelength that is associated with high absorption by a constituent of blood. It this respect, it is practical if the light-receiving unit (25) is configured to receive reflected light back from the volume of fluid (23). The optical analysis may be performed real-time during an action in a person's mouth involving a gum agitation effect, or after such action has taken place, for example.

Disclosed is a sample collection and detection card. A lower cover of the card is provided with a sample loading chamber capable of accommodating a sampling part of a sampling end, an outlet is arranged at a bottom of the sample loading chamber, and a sample loading area of a test strip is located at the outlet; a fixing structure for fixing a sampling rod to a box is further arranged between the box and the sampling rod, and the sampling part is deformable when the sampling rod is fixed to the box. In embodiments of the present disclosure, the sample loading chamber is arranged on the lower cover, and the sample loading area of the test strip is arranged at the outlet of the sample loading chamber.

A method is provided that includes intranasally dispensing nasal wash fluid into a nasal cavity of a subject. Thereafter, a specimen sample is collected by performing an anterior nares nasal swab. The specimen sample is tested for the presence of a virus using a lateral flow immunoassay test strip. Other embodiments are also described.

A sample collection and detection device includes a collection cavity. The device further includes a sample collector. The sample collector comprises a collection rod and an absorption element, and the absorption element has a hollow cavity. A part of the collection rod is received in the hollow cavity of the absorption element. A first lug for blocking and locating the absorption element is arranged on the collection rod. Also provided is a method for collecting and detecting sample using the sample collection and detection device.

Described herein is a portable virometer for detecting viral targets. An exemplary virometer has a molecular electronics sensor with a first electrode, a second electrode spaced-apart from the first electrode by a nanogap, a bridge molecule having a first end and a second end, the first end coupled to the first electrode and the second end coupled to the second electrode, a hybridization probe having an oligonucleotide sequence from or related to a viral target is conjugated to the bridge molecule, a sample applicator for acquiring a sample and transferring it to the chip, and data processing software and hardware for providing a report of detection of viral targets. Methods of using the virometer for testing in the home, in schools, in workplaces, in hotels, in restaurants, or in public places are also described.