A digital pathology apparatus includes a housing with a rail system that allows the housing to slide off of the apparatus to expose the internal elements of the apparatus for easy maintenance. The housing includes a latch and sensor system that securely latches the housing in the closed position and senses when the housing is opened so that the moving parts of the apparatus can be safely stopped to avoid potential injury. The housing also includes electromagnetic shielding on a minimal portion of its interior surface to reduce electromagnetic radiation emanating from the apparatus. The digital pathology apparatus also includes a speakerless audio system that engages with a portion of the interior surface of the housing that is not covered with electromagnetic shielding. The speakerless audio system provides an audio user interface while maintaining a contiguous surface on the housing to cover the digital pathology apparatus.

An apparatus for providing an object to be medically examined by blowing is provided where air is blown into a container in which an object to be medically examined is stored, so as to make the uniform distribution state of the object to be medically examined from the inside of the container, thereby ensuring the sameness of the object to be medically examined, which is to be extracted from the container.

An interactive apparatus, system and method for image capturing and projecting is integrated into an optical microscope. An image capturing and projecting unit is operatively connected to a processing unit, the processing unit configured to: (a) receive user generated data; and (b) overlay the user generated data onto an optically viewed image visible through the eyepiece.

A microscopic optical imaging system for a living cell, relating to the technical field of living cell culture, observation and detection equipment. The microscopic optical imaging system for a living cell includes a sample stage device, a microscopic optical imaging device, a first linear motion device, a second linear motion device, a third linear motion device, and a worktable device. The microscopic optical imaging device is driven by the first linear motion device to move, the sample stage device is driven by the third linear motion device to move, and the microscopic optical imaging device is driven by the second linear motion device to adjust the resolution for imaging, so that the imaging of living cell samples in regions is realized in a non-contact manner and the resolution for imaging is adjusted; meanwhile, the volume of the microscopic optical imaging system for a living cell is reduced.

An optical imaging system for imaging a target during a medical procedure, the imaging system involving an optical assembly having moveable zoom optics and moveable focus optics, a zoom actuator and a focus actuator for positioning the zoom and focus optics, respectively, a controller for controlling the zoom and focus actuators independently in response to received control input, a camera for capturing an image of the target from the optical assembly, the system capable of performing autofocus during a medical procedure.

Systems, methods and devices are implemented for microscope imaging solutions. One embodiment of the present disclosure is directed toward an epifluorescence microscope. The microscope includes an image capture circuit including an array of optical sensor. An optical arrangement is configured to direct excitation light of less than about 1 mW to a target object in a field of view of that is at least 0.5 mm.sup.2 and to direct epi-fluorescence emission caused by the excitation light to the array of optical sensors. The optical arrangement and array of optical sensors are each sufficiently close to the target object to provide at least 2.5 μm resolution for an image of the field of view.

An image capturing device for observing a sample housed in a container to which identification information is attached, from below the container, includes: an image capturing unit including an image pickup element; a light guide unit that guides light from an identification surface to the image capturing unit, the identification surface being a surface of the container which differs from a bottom surface of the container and to which identification information is attached; and a mobile unit that changes a relative position of the image capturing unit with respect to the container. After the mobile unit changes the relative position to a first relative position in which the optical axis of the image capturing unit deviates from the container, the image capturing unit images the identification surface via the light guide unit, and, after the mobile unit changes the relative position to a second relative position in which the optical axis of the image capturing unit intersects the container, the image capturing unit images the sample via the bottom surface.

Embodiments disclosed herein relate to systems and methods for imaging a microscopic sample, for example in a liquid or a solid. The systems can be coupled to a portable electronic device and adjusted in three dimensions to allow for alignment of a lens assembly with an optical axis of a camera on a portable electronic device. This can allow for use across various-sized electronic devices, such as smartphones, tablets, and digital cameras. The systems can have a compact size, which allows for portable and/or at-home analysis of samples. The systems can be used to analyze sperm samples to detect fertility issues. The systems can be used to analyze soil or liquid samples to detect contaminants, such as microplastics.

A method for attaching camera filters and other light transmissive elements using flexural rigidity. A flexion arm enables coupling with cameras and other devices in areas non-proximate to a lens. A frame conjoined with the flexion arm enables attachment of the camera filter to a camera lens or lens housing.

Provided are a tiling light sheet selective plane illumination microscope (TLS-SPIM), a use method thereof and a microscope system. The use method includes loading a corresponding phase map to each group of pupil subsections of a pupil by a spatial light modulator, and performing phase modulation on an excitation beam to create at least two coaxial excitation beam arrays scanning the created at least two coaxial excitation beam arrays to generate discontinuous light sheets accordingly; and tiling at least one of the generated discontinuous light sheets in the propagation direction of the excitation light to obtain tiling light sheets for selective plane illumination of a sample. The method of using the TLS-SPIM, the TLS-SPIM and the system including same enables significant increasing of imaging speed, improvement of resolution, and reduction of source data amount.