Abstract: An ophthalmic surgical microscope (100) has a microscope main objective (101) and a viewing beam path (105) which passes through the microscope main objective (101) for visualizing an object region. The ophthalmic surgical microscope (100) includes an OCT-system (140) for recording images of the object region (108). The OCT-system (140) includes an OCT-scanning beam (142) which is guided via a scan mirror arrangement (146) to the object region (108). An optic element (147) is provided between the scan mirror arrangement (146) and the microscope main objective (101). This optic element (147) bundles the OCT-scanning radiation exiting from the scan mirror arrangement (146) and transfers the same into a beam path which passes through the microscope main objective (101). Alternatively or in addition, the ophthalmic surgical microscope (100) includes an opthalmoscopic magnifier lens (132) which can be pivoted into and out of the viewing beam path (105) and the OCT-scanning beam (142).

Abstract: A surgical microscopy system having an illumination system is provided. The illumination system comprises a xenon gas discharge lamp and a spectral filter which is optionally positionable into an illumination beam path of the surgical microscopy system and removable from the same. The spectral filter substantially exhibits, in a wavelength range between 400 nm and 700 nm, a transmission increasing from about 0.12 to 1 having a gradient between 0.025/nm and 0.0035/nm, in particular 0.00293/nm. Thus, the illumination system is enabled to provide light having two different spectral characteristics which is advantageous in particular for imaging structures in the human eye scattering to a different degree.

Abstract: An optical observation unit (1) has an illumination apparatus (43) for illuminating an observation object (3). The illumination apparatus (43, 143) has a light source (45) emitting illumination light with a first color temperature, and a spectral filter (49) that can be inserted in the illumination beam path. The spectral filter (49) converts the illumination light with the first color temperature into illumination light with a second color temperature. The illumination apparatus further has an attenuator (51) that can be inserted in the illumination beam path in place of the spectral filter (49) and has a transmission characteristic that leads to an intensity reduction of the illumination light with the first color temperature that corresponds to the intensity reduction of the illumination light with the second color temperature by way of the spectral filter (49).

Abstract: A surgical microscope (100) has viewing beams (109a, 109b) passing through a microscope imaging optic which includes a microscope main objective system (101) having a magnification system of variable magnification. The microscope imaging optic transposes a convergent viewing beam (109a, 109b) from the object region (114) into a parallel beam. The surgical microscope includes an OCT-system (120) for examining the object region (114). The OCT-system (120) makes available an OCT-scanning beam (190) which is guided through the microscope imaging optic.

Abstract: A cataract surgery microscopy system is provided which comprises a microscopy optics for producing an image of an object plane of the microscopy optics and a pattern generator for generating a pattern superimposed on the image, said pattern generator being provided to generate a circular pattern having an adjustable diameter.

Abstract: An aperture stop device is provided for use in a microscope with at least one adjustable observation parameter. The aperture stop device includes at least one aperture stop (50a, 50b) with an adjustable aperture, that is to say with an adjustable stop opening. The aperture stop (50a, 50b) is adapted to receive an aperture signal representative of an aperture to be adjusted. In addition the aperture stop device includes a control unit (52) for output of the aperture signal to the aperture stop (50a, 50b) in dependence at least on the respectively set value of the observation parameter of the microscope.

Abstract: First of all, the present invention relates to a light trap (20) for eliminating or preventing stray light, e.g., in the form of scattered light. In addition, the invention relates to a device (10) for coupling a first beam path (34) to a second beam path (42)*. Finally, the invention also relates to an illumination device (30) for an optical observation device as well as an optical observation device. In order to be able to further improve the elimination of disruptive stray light in the form of scattered light, light trap (20) is configured in a special way. It has a filter element (21), particularly a neutral filter element, which is characterized in that incident light face (22) of filter element (21) has a concave radius, whereby incident light face (22) has a specific curvature. * sic; second beam path (41)?—Trans.

Abstract: A process for preparing biodiesel having improved filterability characteristics including inducing transesterification of a triglyceride feedstock with cavitation to form an intermediate reaction product. Glycerol by product is separated from the intermediate reaction product before finishing the transesterification reaction in a pressurized reaction tank to yield a biodiesel reaction product. The biodiesel reaction product can be further purified by removing glycerol.

Abstract: A lighting device (40) is described for an observation device (10), in particular for an ophthalmologic operating microscope, as well as such an observation device (10). The lighting device (40) has a light source (41) as well as a number of optical components, which are provided between light source (41) and an objective element (11). The optical components are designed according to the invention in such a way that the imaging of the lighting pupil (43) and the observation pupils is produced on the fundus of the eye (30). In this way, an exactly defined interaction of the lighting beam path (56) with an observation beam path is made possible, whereby practical requirements can be fulfilled relative to the homogeneity of the red reflex with simultaneous sufficiently good contrasting.

Abstract: A surgical microscopy system having an illumination system is provided. The illumination system comprises a xenon gas discharge lamp and a spectral filter which is optionally positionable into an illumination beam path of the surgical microscopy system and removable from the same. The spectral filter substantially exhibits, in a wavelength range between 400 nm and 700 nm, a transmission increasing from about 0.12 to 1 having a gradient between 0.025/nm and 0.0035/nm, in particular 0.00293/nm. Thus, the illumination system is enabled to provide light having two different spectral characteristics which is advantageous in particular for imaging structures in the human eye scattering to a different degree.

Abstract: Among other things, an illumination device (10) is described for one, two or more observation beam paths, each with an observation device having an observation beam bundle, in particular for an operating microscope, having at least one light source (12) for producing at least one illumination beam bundle for illuminating an object to be observed (13), in particular, an eye to be observed, wherein the at least one illumination beam bundle runs coaxially to an observation beam bundle. It is provided according to the invention, in order to be able to suppress disruptive reflections, that illumination device (10) has an illumination optics (11) that is constructed according to the Köhler principle of illumination, and in which at least one reflection diaphragm (18) is provided in order to avoid light reflected from the surface of an objective element (19). In addition, a correspondingly improved observation device is described.

Abstract: A surgical microscopy system is provided wherein an optical coherence tomography facility is integrated into a microscopy system. A beam of measuring light formed by collimating optics of an OCT system is deflected by a beam scanner, traverses imaging optics, and is reflected by a reflector such that the beam of measuring light traverses an objective lens of microscopy optics and is directed to an object region of the microscopy optics. A position of the beam of measuring light being incident on the reflector is substantially independent on a direction into which the beam of measuring light is deflected by the beam scanner. When traveling through the beam scanner, the beam of measuring light is comprised of a bundle of substantially parallel light rays.

Abstract: The present invention, among other things, relates to a front-lens attachment (20) for an optical observation device (10), in particular for a microscope. The front-lens attachment (20) has a retaining element (38) that has a retaining element (32), on which at least one lens element (33, 34) is disposed. Further, it provides a positioning device (21) for positioning the retaining element (32) and the at least one lens element (33, 34) disposed thereon, relative to the optical observation device (10), whereby retaining device (32) is disposed on positioning device (21). Finally, a fastening means (35) for fastening the retaining device (38) to the front-lens attachment (20) is provided. In order to be able to provide such a front-lens attachment (20) in a structurally simple and cost-effective manner, it is provided, for example, that positioning device (21) has at least two positioning components (22, 28), which are joined together via a joint (31).

Abstract: A microscope arrangement (200) is for viewing an object or an intermediate image, which is generated by an object, especially in microsurgery. The microscope arrangement (200) includes an objective arrangement (201) having an object plane (209) for arranging the object or intermediate image (210) to be viewed. The microscope arrangement has a focus offset adjusting unit (260) which outputs a focusing offset signal in order to defocus in a defined manner the objective arrangement relative to a focusing state.

Abstract: A secondary light source is provided comprising a narrowband light source (11) that emits narrowband light as a primary light source, an optical waveguide (5) having a proximal and a distal end (9), a coupling-in device (13) that is arranged at the proximal end (7) of the optical waveguide (5) and serves for coupling the narrowband light into the optical waveguide (5), and a phosphor region (19) that is present at or before the distal end (9) of the optical waveguide (5), said phosphor region being provided with a converter phosphor. The converter phosphor of the phosphor region (19) is chosen with respect to the narrowband light emitted by the narrowband light source (11) in such a way that it increases the wavelength of at least part of the narrowband light.

Abstract: An optical measuring system, including at least one radiation source; a first beam splitter; a second beam splitter; an OCT detector; a wavefront detector which is different from the OCT detector; at least one active optical element; and a collimator.

Abstract: A surgical microscope (100) has viewing beams (109a, 109b) passing through a microscope imaging optic which includes a microscope main objective system (101) having a magnification system of variable magnification. The microscope imaging optic transposes a convergent viewing beam (109a, 109b) from the object region (114) into a parallel beam. The surgical microscope includes an OCT-system (120) for examining the object region (114). The OCT-system (120) makes available an OCT-scanning beam (190) which is guided through the microscope imaging optic.

Abstract: A surgical microscope (100) has an illuminating arrangement (110) which can guide illuminating light to the object region (105) with a first illuminating beam path (111) and with a second illuminating beam path (112). A light exit unit is provided in the first illuminating beam path (111). An illuminating field diaphragm is mounted in the second illuminating beam path. The first illuminating beam path (111) has an illuminating optic which images the light exit plane of the light exit unit or a plane conjugated to the light exit plane into a first image plane (350). An illuminating optic is provided in the second illuminating beam path (112) and this illuminating optic images the illuminating field diaphragm into a second image plane (250) different from the first image plane.

Abstract: A surgical microscope (1) for ophthalmology includes a tube unit (5) which permits viewing an area (7) of surgery, especially a forward section of the eye, through a microscope main objective (2). The surgical microscope (1) includes an illuminating system (10) which makes available the illuminating light to illuminate the surgical area (7), especially the forward section of the eye. To provide daylight-like illuminating light, the illuminating system includes a xenon illuminating light source (11) or a metal halide illuminating light source. At least one interference filter (22, 23) is provided in the illuminating beam path (16). The cutoff frequency of the interference filter lies such that illuminating light in the ultraviolet range is filtered out and illuminating light in the visible wavelength range is attenuated, if at all, to an insignificant extent in order to reduce the phototoxicity of the illuminating light for the human eye.

Abstract: A surgical microscope (100) has a viewing beam path for main viewing and a secondary beam path (106) for viewing by another person. The surgical microscope (100) has a microscope main objective (101) through which the viewing beam path for main viewing and the viewing beam path (106) for secondary viewing pass. The surgical microscope (100) includes an OCT-system (120) for examining an object region. The OCT-system (120) includes an OCT-scanning beam (123) which is guided through the microscope main objective (101). In the viewing beam path (106) for secondary viewing, an in-coupling element (150) is provided to couple the OCT-scanning beam (123) into the viewing beam path (106) for secondary viewing and to guide the same through the microscope main objective (101) to the object region (108).