Methods and devices for performing minimally invasive procedures useful for Fallopian tube diagnostics are disclosed. In at least one embodiment, the proximal os of the Fallopian tube is accessed via an intrauterine approach; an introducer catheter is advanced to cannulate and form a fluid tight seal with the proximal os of the Fallopian tube; a second catheter inside the introducer catheter is provided to track the length of the Fallopian tube and out into the abdominal cavity; a balloon at the end of the second catheter is inflated and the second catheter is retracted until the balloon seals the distal os of the Fallopian tube; irrigation is performed substantially over the length of the Fallopian tube; and the irrigation fluid is recovered for cytology or cell analysis.

A biopsy device includes an elongated handle body having a proximal end portion and a distal end portion, a needle disposed within the handle body, first and second transducers, and a display. The needle is configured to move between a retracted position and a deployed position. The first and second ultrasound transducers are disposed within the distal end portion of the handle body. The first and second ultrasound transducers are angled relative to one another and define a space therebetween configured for passage of the needle.

The application relates to a sample holder (110) and a system (100). The application also relates to a method for processing a biological sample (S) and use of the sample holder or of the system in an analytical method or a diagnostic method. The sample holder (110) comprises a tubular member (111) with a wall that is at least locally transparent and at least locally permeable for reagents, wherein the tubular member consists at least partially of a transparent material.

Even when an insertion object is inserted to a deep position of a subject or even when the insertion object is inserted into the subject at an angle close to a right angle, it is possible to confirm the position of the insertion object in a photoacoustic image. The insertion object is, for example, a hollow puncture needle 15 that includes an opening at a tip thereof. The puncture needle 15 includes a light guide member 152 that guides light emitted from a first light source to the vicinity of the opening, and a light emitting portion 153 that is provided in the vicinity of the opening and emits the light. First photoacoustic waves, which are caused by the light emitted from the light emitting portion 153, are generated in the puncture needle 15. A first photoacoustic image is generated on the basis of the first photoacoustic waves.

Even when an insertion object is inserted to a deep position of a subject or even when the insertion object is inserted into the subject at an angle close to a right angle, it is possible to confirm the position of the insertion object in a photoacoustic image. The insertion object is, for example, a hollow puncture needle 15 that includes an opening at a tip thereof. The puncture needle 15 includes a light guide member 152 that guides light emitted from a first light source to the vicinity of the opening, and a light emitting portion 153 that is provided in the vicinity of the opening and emits the light. First photoacoustic waves, which are caused by the light emitted from the light emitting portion 153, are generated in the puncture needle 15. A first photoacoustic image is generated on the basis of the first photoacoustic waves.

A method of spectrometric analysis comprises obtaining one or more sample spectra for an aerosol, smoke or vapour sample. The one or more sample spectra are subjected to pre-processing and then multivariate and/or library based analysis so as to classify the aerosol, smoke or vapour sample. The results of the analysis are used for various surgical or non-surgical applications.

A full core biopsy device includes a needle assembly having stylet, spoon, and at least one coring cannula. A window is located in at least one of the spoon and coring cannula. A excising finger is configured to prolapse through the window into a lumen of the inner spoon or cannula to sever a tissue sample upon translation or axial advancement of the excising finger.

A sample container for use in imaging includes a bottom portion and a wall portion extending upwardly from the bottom portion. The lid overlies the cavity when in the closed position, and a plurality of latches are coupled to the lid and extend substantially orthogonally from the lid. A plurality of recesses are coupled to the wall portion, each recess of the plurality of recesses being adapted and configured to receive one of the plurality of latches. A first alignment structure is within the cavity and is adapted and configured to align a sample lengthwise and widthwise within the cavity such that the sample is aligned relative to an imaging system when the sample container is engaged with the imaging system. A second alignment structure is at least partially within the cavity, and is adapted and configured to align the sample height wise within the cavity.

A sample container for use in imaging includes a bottom portion and a wall portion extending upwardly from the bottom portion. The lid overlies the cavity when in the closed position, and a plurality of latches are coupled to the lid and extend substantially orthogonally from the lid. A plurality of recesses are coupled to the wall portion, each recess of the plurality of recesses being adapted and configured to receive one of the plurality of latches. A first alignment structure is within the cavity and is adapted and configured to align a sample lengthwise and widthwise within the cavity such that the sample is aligned relative to an imaging system when the sample container is engaged with the imaging system. A second alignment structure is at least partially within the cavity, and is adapted and configured to align the sample height wise within the cavity.

Methods and systems are provided for reconstruction error assessment for an interventional tool utilized in an image guided interventional procedure. In one example, an error model based on a target lesion position within a tissue, one or more interventional tool parameters, and imaging system parameters may be utilized to estimate an expected reconstruction error for the interventional tool. In another example, when the interventional tool is within the tissue, the expected reconstruction error may be utilized along with observed tool shape and size to infer an actual tool position and shape within the tissue.