Trailers designed for use in transporting timber.

Manufacturing trailers designed for use in transporting timber.

Passenger ground transportation services, Software for scheduling passenger ground transportation services; software for dispatching vehicles for passenger ground transportation

Non-medicated pet cleansing preparations, namely shampoo, coat conditioner, cream rinse, bath oil, and body wash and grooming preparations for veterinary use.

Medicated shampoo, bath oil, coat conditioner and crème rinse for veterinary use

Non-medicated grooming preparations for companion animals.

Driving lights for use on vehicles, namely: headlights, bicycle lights, brake lights for vehicles, cycle lights, illumination lights for registration plates, light bulbs, light fittings, light reflectors, map lights, motorcycle lights; spot lights for use on vehicles, warning lights for vehicles.

Medicated shampoo, bath oil/coat conditioner and creme rinse for veterinary use.

Pharmaceutical preparations for the treatment of diseases and disorders of the alimentary tract and metabolism; pharmaceutical preparations for the treatment of cardiovascular diseases and disorders; pharmaceutical preparations for the treatment of the central nervous system namely central nervous system infections, encephalitis, epilepsy, Alzheimer's, cerebral palsy and Parkinson's disease, brain diseases, central nervous system movement disorders, spinal cord diseases, ocular motility disorders; pharmaceutical preparations for the treatment of psychiatric diseases namely mood, anxiety and cognitive disorders; pharmaceutical preparations for the treatment of urological, urogenital and urinary disorders; pharmaceutical preparations for the treatment of gastrointestinal disorders; pharmaceutical preparations for the treatment of the musculo-skeletal disorders namely connective tissue diseases, bone diseases, spinal diseases, back pain, fractures, sprains, cartilage injuries; pharmaceutical preparations for the treatment of rheumatism; pharmaceutical preparations for the treatment of diabetes, hypertension, erectile dysfunction, sexual dysfunction, stroke, cancer, migraines, pain, obesity, dermatitis, skin pigmentation diseases, sexually transmitted diseases, immunologic diseases, namely autoimmune diseases and immunologic deficiency syndromes, respiratory diseases, and for anti-inflammatories, anti-infectives, hematological preparations, antibacterials, antivirals, antifungals, anti-cholesterol preparations, smoking cessation preparations, tissue and skin repair preparations, ophthalmological preparations and hormonal preparations.

Test systems consisting of (a) test kits, (b) detection units, (c) automation units and (d) 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:(a) 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; (b) with the detection unit comprising: flow cytometer and integrated or external specimen supply station; sheath fluid; flush liquid; cleaning liquid; (c) 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; (d) 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.

1) Test systems consisting of (a) test kits, (b) detection units, (c) automation units and (d) 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:(a) 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;(b) with the detection unit comprising: flow cytometer and integrated or external specimen supply station; sheath fluid; flush liquid; cleaning liquid;(c) 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;(d) 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