An embodiment of the present disclosure provides a liquid collector that collects liquid, the liquid collector including: a flow passage member including a flow passage that connects one end and other end of the flow passage member; a contact member that is disposed at the one end of the flow passage member, that includes an elastic material, and that is configured to come into contact with a target from which liquid is to be collected; and a container that receives the liquid discharged from the flow passage at the other end of the flow passage member.

The present invention provides a device for collecting a fluid specimen. The device comprises a water-absorbing end part formed by bonding a first porous water-absorbing film and a second porous water-absorbing film. Preferably, the second porous water-absorbing film and the first porous water-absorbing film are sponge films.

A set of medical sampling parts for use with an endoscope, including: a sampling device; a sample container including a separator part located at a top of the sample container, a base located at a bottom of the sample container opposite of said top, and a container part at least partly enclosing a sample volume located at the bottom of the sample container, so that a container axis extends between said separator part and said base; and a connector for connecting the sampling device with the sample container, wherein the sample container can be detached from the sampling device by a translational movement along a detachment axis, whereby a smallest angle between said container axis and said detachment axis is equal to or greater than 45 degrees.

An insert for a holding device for reliably and accurately assessing a small volume of blood in a fluid, such as in a volume of surgical fluid collected during a surgical procedure, is provided. The insert may include a circular shelf having an outside perimeter configured to fit up against an inside perimeter of a holding device. The insert may include a center opening. The insert may include a conically-shaped collection cone disposed in the center opening. The collection cone may include a length, an interior surface comprising a red blood cell flocculant coating, a gradually decreasing perimeter terminating in a bottom apex, and a series of graduated volumetric markings along the length of the collection cone.

The present disclosure relates to methods of collecting and testing bacteria containing samples from within the gastrointestinal (GI) tract of a subject. The methods may include disposing an ingestible device in the GI tract, collecting a bacteria-containing sample from the GI tract, selectively lysing eukaryotic cells in the sample by combining the sample with a dried reagent, exposing bacteria in the sample to resazurin in the ingestible device to produce resorufin, emitting light from the ingestible device, the emitted light being filtered through an optical filter to control for scatter so that the light interacts with the resorufin to produce fluorescence, and measuring a total fluorescence from the resorufin; or a rate of change of fluorescence from the resorufin as a function of time within the GI tract of the subject; and correlating the measured parameter to a number of viable bacterial cells in the sample.

Provided herein are methods and a device for collecting biological samples. In particular, the present disclosure relates to a device designed to specifically capture samples within the target areas of a patient for specific cell collection for particular diagnosis.

Provided herein are methods and a device for collecting biological samples from a subject. In particular, the present disclosure relates to a device designed to specifically capture samples within the target areas of a patient for specific cell collection for particular diagnosis.

The present invention relates in general to the improved containment of biological fluids. In particular, a method and apparatus for collection and preservation of fluid samples in accordance with the present invention results in collection of semen having improved viability both at the time of collection and after storage. The disclosed apparatus support a wide variety of applications for containment of biological fluids related to human and veterinary medicine including, but not limited to, human reproductive medicine and animal husbandry.

The present invention relates to a body fluid observation device which enables observation of a user's body fluid. A body fluid observation device according to an example of the present invention comprises: a chamber which has a length in a first horizontal direction and in which a body fluid of a user is stably placed; and a body into which the chamber is inserted for observation of the body fluid. The body comprises: a case including a chamber insertion hole which is formed through the front surface of the body and into which the chamber is inserted, a guide partition wall extending from the chamber insertion hole in the first horizontal direction to guide the chamber, and an observation hole provided through the bottom surface of the body to allow observation of the body fluid; a light source part which is positioned above the chamber in the case and emits light; and an operation part electrically connected to the light source part to operate the light source part, wherein, as the chamber is inserted into the chamber insertion hole, the operation part can form an electrically closed loop for operating the light source part.

The invention relates to an assembly comprising a sampling device with a rod and a swab and a transfer tool for detaching the swab from the rod and transferring the detached swab to a container. The transfer tool comprises a housing enclosing a closed chamber having a swab-member passage and configured for receiving the swab-member. The housing comprises a first housing part and second housing part hinged to the first housing part. The first housing part and second housing part define an entry opening to a channel delimited by the first and second housing part. This channel extends from outside the housing to the passage. The first housing part and second housing part are rotatable around the hinge between a holding condition and a non-holding condition. The swab-member passage is configured to prevent, in holding and non-holding condition, the base from entering the passage whilst allowing, in non-holding condition, the swab member to pass through the passage. The channel and swab are configured to allow, in non-holding condition, inserting the swab-member and the base through the entry opening into the channel, advancing the swab-member to and through the passage into the chamber until the passage prevents the base from entering the passage, and to prevent, in holding condition whilst the passage blocks the base in the insertion direction and the swab-member projects through the passage into the chamber, the base from movement opposite to the insertion direction.