All other goods in International Class 3, 9,16, and 21, including; test systems consisting of test kits, detection units, automation units and software for the examination and/or for the detection of biomolecules and/or of active agents from human, animal or vegetable examination materials, with only one parameter or a plurality of parameters being able to be determined at the same time and/or sequentially in a reaction vessel, with the test kit containing the following parts: reaction vessels, such as vials, microtiter plates or filter plates, with the reaction vessels already being able to contain test components in dried form, preferably in freeze-dried form, in predosed form or with the test components being supplied separately as tablet-shaped compacts in vessels; test components consisting of charged carrier particles (encoded particles which are coated with complementary biomolecules/active agents), conjugates (biomolecules and/or active agents marked with one and/or more characteristic marking values); cover films or covers for the closing of the reaction vessels; vessels with suspensions with charged carrier particles (encoded particles which are coated with complementary biomolecules/active agents); vessels with suspensions with test control particles (encoded particles which are coated with the biomolecule/active agent to be detected); vessels with suspensions with detector control particles (encoded particles which are coated with the conjugate or with the characteristic marking values); vessels with diluting buffers; vessels with conjugate (biomolecules and/or active agents which are marked with one and/or more characteristic marking values); vessel with washing buffers (optional); vessel with reconstitution buffers; vessel with recalibration solution(s) (standard); vessel with positive control / negative control / cut-off control; vessel with reference material; vessel with RF absorbent; vessel with stop solution (optional); quality control certificate with nominal values, tolerance ranges and possibilities to quantify the results; working instructions; kit box; with the detection unit comprising; flow cytometer and integrated or external specimen supply station; sheath fluid; flush liquid; cleaning liquid; with the automation unit comprising; barcode module for the positive identification of specimens, controls, reagents and specific kit parameters; specimen receiving module (e.g. specimen carousel, specimen rack); pipetting module (dilution of the specimens, transfer of controls and reagents); transfer module (repositioning of the samples and of the reaction vessels on the work surface); incubation module (shaker unit, optionally temperature settable); optional washing module; pipette tips; waste containers; and with the software comprising; software for the control of the detection unit; software to accept and analyze the data; software for the control of the automation unit; software for the communication between the detection unit and the automation unit; software for the quantitative evaluation and graphical representation of the data.

All other goods in International Class 3, 9,16, and 21, including; test systems consisting of test kits, detection units, automation units and software for the examination and/or for the detection of biomolecules and/or of active agents from human, animal or vegetable examination materials, with only one parameter or a plurality of parameters being able to be determined at the same time and/or sequentially in a reaction vessel, with the test kit containing the following parts: reaction vessels, such as vials, microtiter plates or filter plates, with the reaction vessels already being able to contain test components in dried form, preferably in freeze-dried form, in predosed form or with the test components being supplied separately as tablet-shaped compacts in vessels; test components consisting of charged carrier particles (encoded particles which are coated with complementary biomolecules/active agents), conjugates (biomolecules and/or active agents marked with one and/or more characteristic marking values); cover films or covers for the closing of the reaction vessels; vessels with suspensions with charged carrier particles (encoded particles which are coated with complementary biomolecules/active agents); vessels with suspensions with test control particles (encoded particles which are coated with the biomolecule/active agent to be detected); vessels with suspensions with detector control particles (encoded particles which are coated with the conjugate or with the characteristic marking values); vessels with diluting buffers; vessels with conjugate (biomolecules and/or active agents which are marked with one and/or more characteristic marking values); vessel with washing buffers (optional); vessel with reconstitution buffers; vessel with recalibration solution(s) (standard); vessel with positive control / negative control / cut-off control; vessel with reference material; vessel with RF absorbent; vessel with stop solution (optional); quality control certificate with nominal values, tolerance ranges and possibilities to quantify the results; working instructions; kit box; with the detection unit comprising; flow cytometer and integrated or external specimen supply station; sheath fluid; flush liquid; cleaning liquid; with the automation unit comprising; barcode module for the positive identification of specimens, controls, reagents and specific kit parameters; specimen receiving module (e.g. specimen carousel, specimen rack); pipetting module (dilution of the specimens, transfer of controls and reagents); transfer module (repositioning of the samples and of the reaction vessels on the work surface); incubation module (shaker unit, optionally temperature settable); optional washing module; pipette tips; waste containers; and with the software comprising; software for the control of the detection unit; software to accept and analyze the data; software for the control of the automation unit; software for the communication between the detection unit and the automation unit; software for the quantitative evaluation and graphical representation of the data.

Computer hardware, namely central processing units, computer peripherals and integrated circuits; computer software for word processing, for table-calculation, for data communication, for database management, for accounting, for business, for video games, for computer graphics and for translation; audio reproduction and audio recording equipment, namely blank magnetic computer tapes and computer discs; electrical communication machines and apparatus, namely radios and satellite dishes; audio frequency apparatus, namely audio tape recorders, audio disk recorders, phonograph record players, compact disc players; CD-ROM drives; CD-R drives; CD-RW drives; written programs for writing data in CD-R and CD-RW; parts and accessories for electrical communication machines and apparatus, namely, microphones; pre-recorded magnetic disks and tapes, phonograph magnetic records and compact disks, all featuring music and voice for educational and entertainment purposes in the fields of mathematics, physics, science, chemistry, languages, poetry, comedy and novels; and other applied electronic machines and apparatus, in INT. CLASS 9.

Pneumatic compression pumps, sleeves, and tubing sets used to help reduce incidence of deep vein thrombosis

Pneumatic compression pumps, sleeves, and tubing sets used to help reduce incidence of deep vein thrombosis

Dietary and nutritional supplements to promote cardio-vascular health.

Hemostatics; wound dressing material; wound sponges; tissue adhesives; biocompatible collagen material, in particular biocompatible collagen membranes, biocompatible collagen matrixes or biocompatible collagen sponges, for use as hemostatic means for surgery; surgical collagen-implants; surgical collagen sponges; the aforesaid products for use in laparoscopy, in particular in laparoscopic surgery.

Haemostatic agent; wound dressing; wound sponge; biocompatible collagen material, in particular biocompatible collagen membrane, biocompatible collagen matrix or biocompatible collagen sponge, for use as a haemostatic agent in surgery; surgical collagen implant; surgical collagen sponge.

Diagnostic reagents for scientific, research, clinical or medical laboratory use; diagnostic preparations for scientific, research, clinical or medical laboratory use for testing blood type genetic markers; diagnostic kits consisting primarily of diagnostic reagents for determining blood type genetic markers for scientific, research, clinical or medical laboratory use; assays for research purposes.

Scientific research in the field of determining blood type genetic markers; laboratory research in the field of determining blood type genetic markers; clinical research in the field of blood type genetic marker science and medicine; medical research in the field of determining blood type genetic markers; technological research in the field of determining blood type genetic markers; laboratory and clinical scientific analysis in the field of determining blood type genetic markers; genetic testing for scientific research purposes; genetic testing services in the field of determining blood type genetic markers for scientific research purposes.

Surgical devices namely, surgical clips and clip appliers

Dietary and nutritional supplements, namely, iron supplements