Abstract: A disinfection cap is described for connection to a medical connector, the disinfection cap includes a housing having a top wall and sidewall forming a cavity, an open cell foam structure disposed within the cavity and a closed cell foam structure disposed against the open cell foam structure, the closed cell foam structure having an interference fit between the closed cell foam structure and the inner surface of the housing. The closed cell foam structure may have a polygonal or star shape, wherein fluid can flow through a gap formed between the closed cell foam structure and the inner surface of the cavity. The open cell foam structure may be impregnated with disinfectant, whereby compression of the open cell foam structure causes excretion of the disinfectant upon insertion of a luer connector.

Abstract: A syringe that includes an adapter section and a barrel having a chamber that holds a fluid. The adapter section includes outer and inner walls that form a first groove. The inner wall includes barrel threads and the outer wall includes a first projection. A cap having cap threads engages the barrel threads to removably attach the cap to the adapter section. A locking element having a sidewall that includes a second projection is received in the first groove and removably attached to the cap by an interference fit. Rotation of the cap causes upward movement of the cap that overcomes the interference fit thereby removing the cap. The locking element is prevented from being removed from the first groove due to contact between the first and second projections. Presence of the locking element in the first groove after the cap is removed provides evidence of tampering.

Abstract: Provided are conductive films including a heparin modified polymer. The heparin modified polymer comprises heparin covalently bound to a beta-substituted monomer having a conjugated backbone that is co-polymerized to its non-functionalized pair. The heparin modified polymer on a conductive film can be manufactured by co-polymerizing a beta-substituted monomer with a non-functionalized monomer to form a polymer on a conductive film. The polymer is reacted with N,N?-Dicyclohexylcarbodiimide (DCC) and acetic acid to form an anhydride of the polymer on the conductive film. The anhydride is then reacted with heparin to form the heparin modified polymer on the conductive film. Medical devices having a coating comprising the conductive film are also described.

Abstract: A method for producing a blister tube having multiple blister pouches with information over a large area and optimized for an inspection system, is provided. A packaging material web having cover sections with a transmission of less than 60% in the visible frequency range extending in the longitudinal direction of the packaging material web, a transparent material area with a transmission of greater than 80% in the visible frequency range extending in the longitudinal direction parallel to the cover sections and to multiple data sections is provided to a packaging device. Pouch-specific data are printed onto a data section and a sub-section of the packaging material web is shaped into a receiving area. A cover section and the printed data section are assigned to each receiving area. Small piece goods are fed to the receiving area and a blister pouch is formed. Devices and blister tubes are also provided.

Abstract: A shield for a needle of a peripheral intravenous catheter or other IV catheter system is provided. The shield may be formed of a single piece of material that may be bent to form a top portion, a bottom portion, a proximal portion, a top distal portion and a bottom distal portion. The proximal portion may form a proximal needle opening and the top or bottom distal portion may form a distal needle opening to allow a needle to extend through the shield when the shield is positioned within the lumen of a catheter adapter. When the distal tip of the needle is withdrawn proximally, the shield may transition from an unlocked position to a locked position in which the distal tip will be retained within the shield.

Abstract: A catheter system may include a catheter adapter, which may include a distal end, a proximal end, a lumen extending through the distal end and the proximal end, and a side port in fluid communication with the lumen. A catheter may extend distally from the catheter adapter. A septum may be disposed within the lumen. The septum may include a first slit generally aligned with a longitudinal axis of the catheter and a second slit offset from the longitudinal axis of the catheter. An introducer needle may be secured within a needle hub and may extend through the catheter and the first slit of the septum. A winged needle set may include: a body; a needle extending distally from the body and through the second slit of the septum; an extension tube extending from the body; and a blood collection device coupled to the extension tube.

Abstract: Disclosed are systems and methods of detecting an impulse of energy given off by an injection device and determining a dosage of medicine based on the impulse. In one example, a module detects the vibrations given off by dialing a click-wheel on an autoinjector and determining the selected dosage of medicine based on the dialed dosage.

Abstract: Particle analyzers having scintillation counters are provided. Particle analyzers of interest include a flow cell for transporting particles in a flow stream, a light source for irradiating a particle in the flow stream at an interrogation point, a particle-modulated light detector for detecting light from the interrogation point, and a scintillation counter for assessing particle radioactivity. In embodiments, the scintillation counter is positioned within the flow cell and configured generate particle radioactivity data that may be associated with a given particle in a plurality of particles. Methods and non-transitory computer readable storage media for practicing the invention are also provided.

Abstract: Aspects of the present disclosure include methods for spectrally resolving light from fluorophores having overlapping fluorescence spectra in a sample. Methods according to certain embodiments include detecting light with a light detection system from a sample having a plurality of fluorophores having overlapping fluorescence spectra and spectrally resolving light from each fluorophore in the sample. In some embodiments, methods include estimating the abundance of one or more of the fluorophores in the sample, such as on a particle. In certain instances, methods include identifying the particle in the sample based on the abundance of each fluorophore and sorting the particle. Methods according to some embodiments includes spectrally resolving the light from each fluorophore by calculating a spectral unmixing matrix for the fluorescence spectra of each fluorophore. Systems and integrated circuit devices (e.g., a field programmable gate array) for practicing the subject methods are also provided.

Abstract: Systems for detecting light (e.g., in a flow stream) are described. Light detection systems according to certain embodiments include a wavelength separator configured to generate first, second and third predetermined spectral ranges of light from a light source and first, second and third light detection modules configured to receive each of the first, second and third predetermined spectral ranges of light, the light detection modules having a plurality of photodetectors and an optical component that conveys light having a predetermined sub-spectral range to the photodetectors. Systems and methods for measuring light emitted by a sample (e.g., in a flow stream) and kits having three or more wavelength separators, a plurality of photodetectors and an optical component are also provided.

Abstract: A medication injection pen comprises a dose set knob rotatable with respect to a housing to set a desired injection dose. The dose set knob comprises at least one internal thread. A leadscrew includes a thread element for advancing in a first direction via a corresponding thread engagement. A driver is rotationally fixed to the leadscrew and is rotatable in a first direction to rotate and advance the leadscrew in the first direction. The setback member is rotationally fixed to the driver. The dose stop member is rotationally coupled to the setback member and is axially movable relative to the dose set knob when the dose set knob is rotated relative to the setback member. Axial movement of the dose stop member limits the user from setting a dose that is greater than an injectable volume of medication remaining in a cartridge.

Abstract: Methods and compositions for detection of vulvovaginal candidiasis (VVC), trichomoniasis and bacterial vaginosis (BV) are disclosed herein. In some embodiments, the presence or absence of VVC-associated Candida, Trichomonas vaginalis, and a plurality of BV-related bacteria in a sample is determined using multiplex nucleic acid-based testing methods.

Abstract: A medicament delivery device comprising a housing connected to a base and enclosing an interior, the interior having a fluid channel wherein the fluid channel passes from a first position in the interior, to a second position outside the interior, and to a third position in the interior.

Abstract: Aspects of the disclosure include a system for performing cytometry that can be operated in three operational modes. In one operational mode, a fluorescence image of a sample is obtained by exciting one or more fluorophore(s) with a top-hat-shaped excitation beam with a plurality of beams that are radiofrequency shifted relative to one another. In another operational mode, a sample can be illuminated successively over a time interval by a laser beam at a plurality of excitation frequencies in a scanning fashion to generate an image of the sample from the detected fluorescence. In another operational mode, the system can be operated to illuminate a plurality of locations of a sample concurrently by a single excitation frequency (e.g., a horizontal extent), which is generated, e.g., by shifting the central frequency of a laser beam by a radiofrequency and detected fluorescence is used to analyze the sample.

Abstract: A delivery device (10) for delivering medicament, such as insulin, to a patient includes a barrel (20), a delivery mechanism (12), and a pump assembly (14). The pump assembly includes a plunger (54), a drive member (56) and a drive screw (58). The plunger is able to slide within a barrel of the device independently of the drive plate. In one embodiment, the plunger is able to slide axially on the drive screw. The medication, such as insulin, can be introduced to the barrel (20) to fill the device and force the plunger to move axially in the barrel into engagement of the drive plate. The drive plate has a threaded aperture that mates with the drive screw. The drive plate engages the plunger by rotation of the drive screw to dispense the medication.

Abstract: A syringe with an integrated vein finder is disclosed, which illuminates a potential venipuncture site of a patient and identifies a vein that is suitable for venipuncture with the syringe, for blood collection or intravenous drug administration. The syringe portion of the system includes a syringe barrel and a pointed-tip needle projecting from the distal end of the barrel for venipuncture. An illumination module is coupled to the syringe barrel; it has an illumination source that projects an electromagnetic beam into an illumination zone distal the syringe's pointed tip, for illuminating and identifying a subcutaneous vein. The integrated vein finder and syringe system is operable by a sole clinician, such as a phlebotomist, who can easily manipulate the syringe and illuminate the venipuncture site with one hand, without assistance of another clinician.

Abstract: An integrated disinfection device is described syringe assembly having two integrated disinfection units assembled to a syringe for disinfecting and sterilizing corresponding medical connectors, specifically access ports of corresponding medical connectors. The integrated disinfection unit includes a first cup and a second cup. The first cup having a chamber containing a first absorbent material, a first disinfectant or an antimicrobial agent in the first cup, and a first peelable seal. The second cup having a chamber containing a second absorbent material, a second disinfectant or an antimicrobial agent in the second cup, and a second peelable seal. A threaded connection is disposed on the bottom exterior surface of the first cup having threads that are sized and pitched to engage threads of a luer lock collar on the distal end of the syringe barrel to allow the first cup to be connected to the syringe assembly.

Abstract: A needle hub including a core mounting structure, a first panel and a second panel each connected to the core mounting structure with an opening formed between the first panel and the second panel, and an introducer needle fixedly attached to the core mounting structure; a first actuation lever disposed within the opening, cantilevered at a central portion thereof from the core mounting structure that has a first actuation button disposed at a proximal free end and a first needle hub latch disposed at a distal free end. A needle tip shield is rotatably connected to one of the first panel and the second panel and rotatable from a first position in which a distal end of the introducer needle is exposed to a second position shielding the distal end of the introducer needle.