摘要:
A lancet structure (606) for a lancet housing assembly (600) of a portable handheld medical diagnostic device (10) for sampling bodily fluids from a skin site of a patient, wherein the lancet structure is adapted to be located in a lancet compartment (605), the lancet structure comprising a skin penetrating end (608) and a blood transport portion (610) adjacent the skin penetrating end, wherein the skin penetrating end, when extended through an opening (636) of the lancet compartment, is shaped and sized to penetrate the patient's skin at the skin site to provide an amount of blood, the blood transport portion arranged and configured to receive the amount of blood from the skin penetrating end and to carry the amount of blood away from the skin site and to a reagent material (650) located on a floor (70, 84) of the lancet compartment and within the lancet compartment, wherein the lancet structure includes an outwardly extending spring finger (616) that extends upwardly at an upwardly extending portion (618) and longitudinally at a longitudinally extending portion (620), wherein a bend (622) connects the upwardly extending portion and longitudinally extending portion.
摘要:
Die vorliegende Erfindung betrifft ein Implantat (110) zum Nachweis mindestens eines Analyten (126) in einer Körperflüssigkeit, insbesondere einer Augenflüssigkeit, wobei das Implantat (110) eingerichtet ist, um in ein Körpergewebe eines Patienten, insbesondere eine Gewebeschicht und/oder eine Kammer eines Auges des Patienten, implantiert zu werden, wobei das Implantat (110) eine Hydrogelmatrix (110) mit mindestens einem Hydrogel (114) aufweist, wobei das Implantat (110) weiterhin in der Hydrogelmatrix (110) homogen dispergierte Sensorpartikel (116) aufweist, wobei die Sensorpartikel (116) mindestens eine Sensormatrix (120) mit einem Sensormatrixmaterial (122) und mindestens ein Sensormaterial (124) aufweisen, wobei das Implantat (110) weiterhin mindestens eine zumindest weitgehend Analyt-invariante Referenzkomponente (132) aufweist, wobei die Referenzkomponente (132) homogen in der Hydrogelmatrix (110) dispergiert ist.
摘要:
The invention relates to a method for training of personnel in quality control for the filling of amorphous products (128) into primary packaging means (118). The method comprises the following steps: a) at least one providing step, wherein, in the providing step, at least one test set (112) of filled primary packaging means (118) is provided, the test set (112) comprising a plurality of primary packaging means (118) filled with the amorphous product (128), wherein at least one primary packing means (118) of the filled primary packing means (118) is affected with at least one impurity (138), the impurity (138) comprising at least one fluorescent marker (142); b) at least one training step, wherein, in the training step, the test set (112) is presented to at least one person to be trained, the person to be trained carrying out a visual quality control for detecting impurities (138), wherein the result of the training step is documented; c) at least one verification step, wherein, in the verification step, the test set (112) is irradiated with excitation light (116), in which fluorescent impurities (138) are detected and wherein the result of the verification step is documented; and d) at least one comparison step, wherein, in the comparison step, the result of the training step and the result of the verification step are compared.
摘要:
A closure (170) for a vial (100) comprising a vial container (110) and a sealing (280). The closure (170) comprises a body (180), at least one holding element (190) adapted to hold the closure (170) permanently secure on the vial container (110) and such that the sealing (280) is adapted to provide a tight connection between the vial container (110) and the body (180), a penetrable portion (290) adapted to allow a liquid transfer is disclosed and a cap (200) adapted to provide a germ free protection of the penetrable portion (290), wherein the body (180) and the penetrable portion (290) are integrally formed. Further, a vial (100) with such a closure (170), a method for closing a vial container (110) with such a closure (170) and a method for manufacturing such a closure (170) are disclosed.
摘要:
The present invention discloses a method for a reversible alteration of a magnetic state of a material. According to a step a), an electrochemical cell with at least one first electrode of a first polarity and at least one second electrode of a second polarity opposing the first polarity is provided, wherein the at least one first electrode at least comprises a ferromagnetic host material with intercalation sites for a reception of non-magnetic atoms, and wherein the at least one second electrode at least comprises an amount of the non-magnetic atoms. According to a step b), the electrochemical cell is consecutively charged and/or discharged to allowing at least a part of the amount of the non-magnetic atoms to move between the intercalation sites the host material and the second electrode, by which movement the magnetic state of the material is reversibly altered. Hereby, the host material comprises a structure which is retained during the alteration of the magnetic state of the material. Further, a device for a reversible alteration of a magnetic state of a material, particularly for performing the method described above, is disclosed. The device is particularly used as part of a magnetic valve and/or of a magnetic shutter and/or of a magnetic sensor and/or a part thereof and/or in an array comprising magnetic beads and/or for magnetic manipulation and/or magnetic guidance and/or magnetic sorting of inorganic, organic or biological substances or a mixture thereof which may react to magnetic phenomena, especially in microfluidics.
摘要:
A test element (110) for detecting at least one analyte in a body fluid is disclosed. The test element (110) comprises a housing (112) having at least one base element (114) and at least one cover element (116). The test element (110) further comprises at least one fluid channel (124) formed within the housing (112). The fluid channel (124) comprises a capillary region (126) and a measurement region (130), wherein the capillary region (126) and the measurement region (130) have differing aspect ratios. The cover element (116) comprises at least one test field (138) having at least one test chemical (140). The test chemical (140) is adapted to change at least one optically measurable property in the presence of the analyte. The cover element (116) is mounted to the base element (114) by using at least one adhesive (134) which contacts the test field (138).