A test device by immunochromatography comprises a case including a dropping window for a specimen and a detection window, and a test piece in the case. The test piece includes first and second detection portions, and a dropping area common to the first and second detection portions. When the specimen is dropped on the dropping area through the dropping window, the specimen migrates downstream and the same specimen reaches the first and second detection portions. The first detection portion traps a complex of a first labeled body and a first antibody contained in the specimen. The second detection portion traps a complex of a second labeled body and a second antibody contained in the specimen. The first antibody is produced by vaccination or infection with a predetermined virus. The second antibody is produced by infection with the virus. Thus, a test result from each of the first and second detection portions, both visually observed through the detection window, can be determined in parallel and at the same time.
The purpose of the present invention is to provide a test instrument and a test method using immunochromatography, by which the efficacy of vaccination against a specific virus such as new coronavirus can be rapidly and easily determined. A test instrument 10, which uses immunochromatography, comprises a fist test strip 11, a second test strip 12 which is different from the first test strip 11, and a case 13 in which the first and second test strips 11 and 12 are integrally housed. The case 13 is provided with a specimen drop window 103, a first detection window 131 through which a portion of the first test strip 11 is visible from the outside, and a second detection window 132 through which a portion of the second test strip 12 is visible from the outside. The first test strip 11 enables the detection of the presence of a first antibody in a specimen. The second test strip 12 enables the detection of the presence of a second antibody, which is different from the first antibody, in the specimen. Due to this structure, the result of the first test strip 11 visually confirmed through the first detection window 131 and the result of the second test strip 12 visually confirmed through the second detection window 132 can be determined simultaneously in parallel.
C12Q 1/70 - Measuring or testing processes involving enzymes, nucleic acids or microorganismsCompositions thereforProcesses of preparing such compositions involving virus or bacteriophage
A test device and a test method are provided which can prevent a specimen liquid from splattering and leaking and perform an examination simply and safely. The test device includes a culturing unit configured to be capable of culturing a specimen in a sealed state, a test piece configured to be capable of absorbing a specimen liquid in the culturing unit, a separating unit configured to be capable of separating the test piece and the specimen liquid in a non-contact state, an opening unit configured to be capable of opening at least a portion of the separating unit to form a flow path through which the specimen liquid reaches the test piece, and a case configured to integrally seal at least a portion of the test piece on a side closer to the separating unit, at least a portion of the culturing unit, and the separating unit.
The purpose of the present invention is to provide a test device and a test method which are capable of preventing a specimen liquid from being scattered and leaked, and simply and safely performing an inspection. This test device 10 is provided with: a cultivation means 11 capable of cultivating a specimen in a sealed state; a test piece capable of absorbing a specimen liquid S2 cultivated by the cultivation means; a separation means 15 capable of separating the test piece 13 and the specimen liquid S2 in a noncontact state; an opening means 17 capable of forming a fluid passage, through which the specimen liquid S2 reaches the test piece 13, by opening at least a portion of the separation means 15; a case which integrally seals at least a separation means 15-side portion of the test piece 13, at least a portion of the cultivation means 11, and the separation means.
A cuff pressure adjusting device includes: a gas feeding unit which feeds a gas into a cuff by a pressing manipulation performed by a user; a cuff pressure detection unit which detects a pressure in the cuff; and a display unit which displays the pressure detected by the cuff pressure detection unit. The gas feeding unit includes: an elastic hollow body which is deformed so as to reduce an inner volume with reception of a pressing manipulation; and a support member which is disposed adjacently to the elastic hollow body in a direction along which the pressing manipulation is performed.
Medical apparatus and instruments [other than walking aids,
crutches]; diagnostic apparatus and instruments; oxygen
concentrators for medical purposes; oxygen inhalators for
therapeutic purposes; esthetic massage apparatus for
commercial use; electric massage apparatus for household
purposes; gloves for medical purposes.
[Problem] To provide a cuff pressure adjustment device having improved convenience of use and improved safety. [Solution] A cuff pressure adjustment device 1 is provided with: a gas delivery section 10 which delivers gas into a cuff 103 on the basis of pressing operation by the user; a cuff pressure detection section 30 which detects pressure within the cuff 103; and a display section 60 which displays the pressure detected by the cuff pressure detection section 30. The gas delivery section 10 is provided with: an elastic hollow body 14 which, when subjected to the pressing operation, deforms so that the inner volume of the elastic hollow body 14 decreases; and a support member 12 which is disposed adjacent to the elastic hollow body 14 in the direction of the pressing operation.
An object of the present invention is to provide a system for performing objective examination of central sensitization, in particular, a system for objectively determining the presence or absence of central sensitization in a chronic pain patient. The present invention provides a device for diagnosing the presence or absence of central sensitization, the device including: stimulation output means for outputting thermal stimulation which can be perceived by a subject; first input means capable of inputting a measurement start signal; second input means capable of inputting a measurement end signal; and measurement control means for measuring time between an input signal from the first input means and an input signal from the second input means. The measurement control means determines that the central sensitization is present when the time between the input signal from the first input means and the input signal from the second input means is longer than t seconds (where t represents 30 seconds or more and less than 90 seconds).
In the present invention, a nail-resin-curing light radiation apparatus (1) comprises a belly side cover member (20), a nail side cover member (30), and a light source (40). The belly side cover member (20) faces the belly of a fingertip. The nail side cover member (30) is disposed so as to cover at least a nail on the fingertip. The light source (40) radiates light on the nail. In the belly side cover member, an accommodation unit (22) is formed at least in the vicinity of the fingertip, the accommodation unit (22) accommodating a part (12) of a nail resin holding member provided in the fingertip. As a result, it is possible to provide a nail-resin light radiation apparatus which is highly convenient to a user.
09 - Scientific and electric apparatus and instruments
10 - Medical apparatus and instruments
Goods & Services
Measures; weighbridges; weighing apparatus and instruments;
weighing machines; laboratory apparatus and instruments;
photographic machines and apparatus; cinematographic
machines and apparatus; optical machines and apparatus;
measuring or testing machines and instruments; electric or
magnetic meters and testers; telecommunication machines and
apparatus; electronic machines, apparatus and their parts;
buzzers, electric. Massage apparatus for medical purposes; inhalers;
sphygmomanometers; sphygmotensiometers; arterial blood
pressure measuring apparatus; thermometers for medical
purposes; medical apparatus and instruments; electric
massage apparatus for household purposes.
A syringe-operation detection device (1) for detecting an extraction or injection operation performed on the plunger (120) of a syringe (100). A female connector (52) is attached to the tip (116) of the barrel of the syringe (100), a male connector (60) is attached to the base (132) of a hypodermic needle (130), and a connecting vessel (70) is connected between said female connector (52) and male connector (60) so as to be closed to the outside. A detector that detects the pressure, flow velocity, or flow rate of a fluid moving through said detector is provided in the connecting vessel (70), the female connector (52), or the male connector (60). This allows the provision of a syringe-operation detection device that can be applied to a syringe that will actually be used and makes it possible to objectively determine how well extraction or injection is performed.
[Problem] To provide a touch perception sensitising glove with which an examination by means of palpation can be smoothly and precisely carried out, and which enables a fingertip to be moved smoothly across a wide area without influencing minute touch perception. [Solution] This touch perception sensitising glove (1) detects the minute irregularities of an object being examined, via a sensitising layer (2), by means of a hand inserted between the sensitising layer (2) and an external cover (3); therein, the sensitising layer (2) is provided with a first film (10) which comes into contact with the object being examined, a second film (12) which is laminated on the first film (10), and an air induction opening (14) which introduces air between the first film (10) and the second film (12) and which enables the second film (12) to slide relative to the first film (10); the external cover (3) or the sensitising layer (2) is provided with a stopper (20) which positions a fingertip of a hand, being inserted between the sensitising layer (2) and the external cover (3), on the inner side of the peripheral edge of the sensitising layer (2).
A61B 10/00 - Instruments for taking body samples for diagnostic purposesOther methods or instruments for diagnosis, e.g. for vaccination diagnosis, sex determination or ovulation-period determinationThroat striking implements
A touch sensitization glove (1), comprising a sensitizing layer (2) and an external cover (3). The sensitizing layer (2) further comprises a first film (10) coming into contact with an object, a second film (12) superposed on the first film (10), and an air inlet (14) leading air between the first film (10) and the second film (12). The second film (12) is allowed to slidably move on the first film (10). Thus, lubricant can be eliminated, and an advanced touch sensitization glove can be provided.
