A system and method for measuring the percent fill of a blood sampling capillary includes a chamber for receiving a sample capillary containing a blood sample, an illuminator arranged to illuminate the sample capillary, an imaging lens aligned with the chamber and the sample capillary, an image sensor aligned with the imaging lens wherein the image sensor receives an image of the blood in the sample capillary from the imaging lens and converts the image to image data, a micro-controller circuit electrically coupled to the image sensor, and at least one of a host computer or a user interface electrically coupled to the micro-controller unit where the micro-controller circuit processes the image data into a percent fill result where the percent fill result is passed to the at least one of the host computer or the user interface.

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.

A medical device includes a housing that has a front face and a side face. The housing defines a window cavity on the front face and a button cavity in the side face. A display is disposed in the housing. The display is aligned in the housing for viewing through the window cavity. A window covers the display in the window cavity, and the display is at least partially visible through the window. The window extends along the front face to the button cavity in the side face. A button element is received in the button cavity. The button element and the window are separate components. The button element has opposing end edges that align with the end edges of the window where the button element and window meet to provide an impression that the window and the button element are integral with one another.

A needle assembly, such as a catheter assembly, having a needle shaft with a needle tip formed from a first rigid material for puncturing a subject. The shaft section, proximal of the needle tip can be formed from a second material different from the first material. The needle tip is attached to the needle shaft to form the needle. The first material can have higher rigidity than the second material and the needle can project through a catheter tube and used in a catheter assembly.

An evacuated container assembly suitable for use in connection with blood collection including: (a) a container member formed of a first polymeric material and having a sidewall and one or more openings; (b) a nanocomposite barrier coating disposed on the container member having a thickness of up to about 30 microns and being derived from an aqueous dispersion including (i) a dispersed barrier matrix polymer; and (ii) a substantially exfoliated silicate filler having an aspect ratio of more than 50; and (c) one or more sealing members disposed in the opening(s) operative to hermetically seal the cavity; wherein the cavity is evacuated and maintains a pressure below atmospheric pressure and exhibits a draw volume loss lower than that of a like assembly without a nanocomposite barrier film by a factor of at least 1.5.

The present disclosure is directed to a needle assembly for drawing blood. The needle assembly can be a standalone or part of an over-the-needle medical device, such as an intravenous catheter. A blood collection device is attached directly or indirectly to the needle hub of the needle assembly and/or to a catheter hub, such as through a Y-site or adaptor connected to a tubing that is connected to the catheter hub. The needle is configured to access the vascular system to draw blood, which then passes to the blood collection device via the needle lumen, which has a tip having a discontinuity opening, an opening with a movable stem, or a shaft element with a lumen.

Embodiments of the present disclosure generally relate to apparatuses for sampling bodily fluids and methods of fabrication thereof. The apparatus includes at least one adhesive patch, at least one bodily fluid port attached to the adhesive patch, and at least one bodily fluid storing capillary connected to the bodily fluid port and attached to the adhesive patch. The adhesive patch may be adhered to a subject's skin, the input port may then be connected to a source of bodily fluids and the one or more bodily fluid storing capillaries function to draw in the bodily fluid over time and store it for later analyzation. The one or more bodily fluid storing capillaries may be formed by imprint lithography on a plastic or glass substrate.

The present invention provides an automatic blood-sampling tube preparation system which can reduce the reading mistake of the information of the RFID tags by selectively taking out a blood-sampling tube required to an examination of a patient according to a doctor's instruction information from the blood-sampling tube containing section, writing the patient examination information on a RFID tag of the taken out tube on the basis of the instruction information, reading simultaneously all patient examination information from all RFID tags contained in the prepared container for every patient, and comparing the information read from the RFID tags with the instruction information to ensure accuracy.

A system acquiring body fluid samples is provided. One embodiment comprises a housing with a sampling channel extending therethrough and defined by an inlet port and an outlet port, wherein the inlet port secures a needle that penetrates a patient; a diversion chamber body portion directly secured to the housing with at least one diversion chamber, wherein the diversion chamber is in fluid communication with the sampling channel, wherein an initial first portion of the body fluid received from the needle is transferred through the sampling channel inlet port and into the diversion chamber, and wherein a subsequent second portion of the body fluid received from the needle is communicated through the sampling channel to the outlet port for collection into a collection device while the initially received first portion of the body fluid is retained in the diversion chamber.

A fluid handling device includes a receiving container with a piston arranged therein in a displaceable manner, such that the volume of a fluid receiving reservoir may be changed by a displacement of the piston. In addition, the fluid handling device includes an actuation mechanism configured to displace a carrier bearing upon actuation of the former. Finally, the fluid handling device includes a spring mechanism configured to transfer a force from the carrier bearing to the piston so as to effect, in response to displacement of the carrier bearing in a first direction, a displacement of the piston within the receiving container such that a volume of the fluid reservoir is increased.