An automated method of evaluating a collected fluid sample includes: filling a sample cavity with the collected fluid sample; adding a buffer solution; separating the collected fluid sample into a first portion and a second portion; mixing the second portion with tagged antibodies; removing leftover tagged antibodies; and measuring a difference between the first portion and the second portion. A sample collection and testing device includes: a reference cavity comprising a reference fluid sample; a test cavity comprising a test fluid sample; a reference measurement element associated with the reference cavity; and a test measurement element associated with the test cavity. A method of evaluating a collected fluid sample including: separating the sample; pumping a first portion to a first measurement cavity; adding a solution to a second portion and pumping the mixture to a second measurement cavity; and measuring a charge difference between the first and second measurement cavities.

A system is provided for monitoring analyte in a host, including a continuous analyte sensor that produces a data stream indicative of a host's analyte concentration and a device that receives and records data from the data stream from the continuous analyte sensor. In one embodiment, the device includes a single point analyte monitor, from which it obtains an analyte value, and is configured to display only single point analyte measurement values, and not any analyte measurement values associated with data received from the continuous analyte sensor. Instead, data received from the continuous analyte sensor is used to provide alarms to the user when the analyte concentration and/or the rate of change of analyte concentration, as measured by the continuous analyte sensor, is above or below a predetermined range. Data received from the continuous analyte sensor may also be used to prompt the diabetic or caregiver to take certain actions, such as to perform another single point blood glucose measurement. In another embodiment, the device provides for toggling between two modes, with one mode that allows for display of glucose concentration values associated with the continuous glucose sensor and a second mode that prevents the display of glucose concentration values associated with the continuous glucose sensor.

A biological fluid sampling transfer device adapted to receive a multi-component blood sample is disclosed. After collecting the blood sample, the biological fluid sampling transfer device is able to separate a plasma portion from a cellular portion. After separation, the biological fluid sampling transfer device is able to transfer the plasma portion of the blood sample to a point-of-care testing device. The biological fluid sampling transfer device also provides a closed sampling and transfer system that reduces the exposure of a blood sample and provides fast mixing of a blood sample with a sample stabilizer. The biological fluid sampling transfer device is engageable with a blood testing device for closed transfer of a portion of the plasma portion from the biological fluid sampling transfer device to the blood testing device. The blood testing device is adapted to receive the plasma portion to analyze the blood sample and obtain test results.

A medical device with a capacitive sensing function includes a medical body having a syringe and a sensing circuit having an electrode, a protective film adhered to the medical body and including a plastic film, an electrode provided on the plastic film and opposite from the electrode of the medical body, and a capacitive sensor formed by the electrode of the medical body and the electrode of the protective film and being a part of the sensing circuit, wherein a capacitance value of the capacitive sensor changed under the condition of removing the protective film from the medical body, the sensing circuit being configured to detect the capacitance value and trigger corresponding function of the medical body.

Various medical systems and methods are described, including a medical monitoring system. The medical monitoring system can have a fluid system configured to receive bodily fluid and optically analyze said fluid to determine analyte concentration. The fluid system can have a removable portion. The removable portion can have an opening with a port. The system can also have a container configured to contain anticoagulant. The container can have a portion configured to mate with the port of the removable portion. The container can be further configured to not fit into a conventional luer fitting. An anti-coagulant insertion apparatus is also described. The apparatus can have a syringe, a dock with a port, and an adapter configured to connect the syringe to the port. The dock can also have a tab configured to move with the port.

An apparatus, system, and method for sampling a fluid from a tissue site is described. The system includes a collection fitting, a reduced-pressure source, and a specimen container. The collection fitting includes a tee-fitting having a first arm having a first union, a second arm having a second union, and a third arm. At least one lumen extends through the tee-fitting from the first arm to the third arm, and at least one lumen extends through the tee-fitting from the second arm to the third arm. A container union is coupled to the third arm. The reduced-pressure source is configured to be fluidly coupled to the first union, and the specimen container is configured to be coupled to the container union.

Systems and method are disclosed for determining a concentration of an analyte in a fluid (e.g., blood). The system can draw blood from a patient and deliver the blood to a sample cell. A particular component of the fluid (e.g., plasma) may be separated and/or positioned such that the concentration of the analyte is measured in the particular component of the fluid (e.g., plasma). The sample cell can include a sample container that has two window pieces. The system can have a fluid passage having a tip configured to mate with a multi-lumen catheter without leaking. The multi-lumen catheter can have proximal and distal ports. A fluid pressure system can be configured to periodically draw fluid from vasculature through a proximal intravascular opening and the proximal port while maintaining a low pressure and/or flow rate to thereby reduce risk of reversing the fluid flow in a vessel and drawing infusates upstream into another intravascular opening.

An apparatus includes a catheter, an introducer, and an actuator. A distal end portion of the introducer has a lock configured to couple the introducer to a closed system intravenous line at least partially disposed in a body. The lock is configured to transition a seal of the closed system intravenous line from a closed state to an open state when coupled thereto. The actuator is at least partially disposed in the introducer and coupled to a proximal end portion of the catheter. The actuator is configured to move the catheter between a first position, in which the catheter is disposed within the introducer, and a second position, in which the catheter extends through the seal of the closed system intravenous line such that a distal end surface of the catheter is positioned distal to the closed system intravenous line.

A blood collection set to couple to a catheter system may include a needle assembly and/or a housing. The needle assembly may include a body, a sharp needle extending proximally from the body, and a sheath covering a proximal tip of the sharp needle. The housing may be coupled to a distal end of the needle assembly. The housing may be configured to create a fluid path through a connector of the catheter system.

A container assembly is disclosed including an outer container, a hollow inner member, and a closure. The outer container has a closed bottom, an open top, and a sidewall extending therebetween. The hollow inner member is disposed within the outer container and has an inner surface defining at least one capillary channel. The inner member includes a first end adjacent to the open top of the outer container and has an outer periphery seated against the sidewall of the outer container. The closure has a proximal end and a distal end. The closure proximal end is seated at least partially within the first end of the inner member to seal the outer container and inner member and define a fluid collection chamber. The closure distal end defines a recessed area shaped to direct fluid under capillary action to the at least one capillary channel in the inner member.