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Table of contents:

• Document 78645476 overview
• GOODS AND/OR SERVICES CLASS
• PROSECUTION HISTORY
• Document 77923116 overview
• GOODS AND/OR SERVICES CLASS
• FOREGIN REGISTRATION
• PROSECUTION HISTORY

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Trademark domain
name	is free?
mondobiotech.com

The "MONDOBIOTECH" trademark, serial number 78645476 , was filed on 7th of June 2005 with a mark drawing code of 4000 and its transaction date is 78645476. The attorney assigned is Gregory Turocy, attorney docket number ARTHT103US. Since 31st of December 2009, the document can be found in the L30 law office in the publication and issue section. The employee responsible is SPARACINO, MARK V and the date it was published for opposition on 10/10/2006. The date when we last checked the status of this trademark was 02/02/2009.

The corresponded responsible for this trademark is Gregory Turocy, located at AMIN, TUROCY & CALVIN, LLP, 1900 E. 9TH STREET, 24TH FLOOR, NATIONAL CITY CENTER.

The state or country where the trademark was organized is by Mondobiotech Holding Sa. The legal entity type behing it is a Corporation, located at Aeschengraben 9, Ch-4051 Basel, zip .

GOODS AND/OR SERVICES
International Class - 001 - Chemicals used in industry, science and photography, as well as in agriculture, horticulture and forestry; unprocessed artificial resins; unprocessed plastics; manures; fire extinguishing compositions; tempering and soldering preparations; chemical substances for preserving foodstuffs; tanning substances; adhesives used in industry.
U.S. Class	046 - Foods and Ingredients of Foods
Class Status	6 - Active
Status Date	06/13/2005
Primary Code	001
International Class - 005 - Pharmaceutical and veterinary preparations; sanitary preparations for medical purposes; dietetic substances adapted for medical use, food for babies; plasters, materials for dressings; material for stopping teeth, dental wax; disinfectants; preparations for destroying vermin; fungicides, herbicides.
U.S. Class	052 - Detergents and Soaps
Class Status	6 - Active
Status Date	06/13/2005
Primary Code	005
International Class - 035 - Advertising; business management; business administration; office functions.
U.S. Class	102 - Insurance and Financial
Class Status	6 - Active
Status Date	06/13/2005
Primary Code	035
International Class - 042 - Scientific and technological services and research and design relating thereto; industrial analysis and research services; design and development of computer hardware and software.
U.S. Class	101 - Advertising and Business
Class Status	6 - Active
Status Date	06/13/2005
Primary Code	042
International Class - 044 - Medical services; veterinary services; hygienic and beauty care for human beings or animals; agriculture, horticulture and forestry services.
U.S. Class	101 - Advertising and Business
Class Status	6 - Active
Status Date	08/08/2006
Primary Code	044
Goods codes
GS0011	Diagnostic preparations for scientific or research use; diagnostic preparations other than for medical or veterinary purposes; chemical preparations for use in science
GS0051	Pharmaceutical preparations for the treatment of infectious diseases; pharmaceutical preparations for the treatment of non-infectious diseases, namely immunological diseases, autoimmune diseases, cardiovascular diseases, inflammatory diseases, and neurodegenerative diseases; pharmaceutical preparations for treating respiratory diseases and asthma; pharmaceutical preparations for treatment of pulmonary diseases; pharmaceutical preparations for the treatment of hypertension; pharmaceutical preparations for use in the treatment of cancer; pharmaceutical preparations for use in chemotherapy; pharmaceutical preparations for rare diseases, namely ACTH Deficiency; AIDS (Acquired Immune Deficiency Syndrome); AIDS Dysmorphic Syndrome; APECED Syndrome; Aarskog Syndrome; Aase Syndrome; Abetalipoproteinemia; Ablepharon Macrostomia Syndrome; Acanthocheilonemiasis; Acanthocytosis; Acanthosis Nigricans; Achalasia; Achard Thiers Syndrome; Achondrogenesis; Achondroplasia ; Acidemia, Isovaleric; Acidemia, Methylmalonic; Acidemia, Propionic; Acne Rosacea; Acoustic Neuroma; Acquired Aplastic Anemia; Acrocallosal Syndrome, Schinzel Type; Acrodermatitis Enteropathica; Acrodysostosis; Acromegaly; Acromesomelic Dysplasia; Acromicric Dysplasia; Acute Respiratory Distress Syndrome; Adams Oliver Syndrome; Addison's Disease; Adenoid Cystic Carcinoma; Adenylosuccinate Lyase Deficiency; Adie Syndrome; Adrenal Hyperplasia, Congenital (General); Adrenoleukodystrophy; Afibrinogenemia, Congenital; Agammaglobulinemias, Primary; Agenesis of Corpus Callosum; Agnosia, Primary Visual; Agranulocytosis, Acquired; Ahumada-Del Castillo Syndrome; Aicardi Syndrome; Alagille Syndrome; Albinism; Alexander Disease; Alkaptonuria; Allan Herndon Syndrome; Alopecia Areata; Alpers Disease; Alpha-1-Antitrypsin Deficiency; Alpha-Mannosidosis; Alport Syndrome; Alstrom Syndrome; Alternating Hemiplegia of Childhood; Alveolar Capillary Dysplasia; Alveolar Soft Part Sarcoma; Alveolitis, Extrinsic Allergic; Alzheimer's Disease; Ameloblastoma; Amelogenesis Imperfecta; Amenorrhea, Primary; Amenorrhea-Galactorrhea Syndrome; Amniotic Bands; Amyloidosis; Amyotrophic Lateral Sclerosis; Anaphylaxis; Andersen Disease (GSD IV); Androgen Insensitivity Syndrome, Partial; Anemia, Blackfan Diamond; Anemia, Fanconi's; Anemia, Hemolytic, Acquired Autoimmune; Anemia, Hemolytic, Cold Antibody; Anemia, Hemolytic, Warm Antibody; Anemia, Hereditary Nonspherocytic Hemolytic; Anemia, Hereditary Spherocytic Hemolytic; Anemia, Megaloblastic; Anemia, Pernicious; Anemias, Sideroblastic ; Anencephaly; Angelman Syndrome; Angioedema, Hereditary; Aniridia; Aniridia Cerebellar Ataxia Mental Deficiency; Ankylosing Spondylitis; Anodontia; Anorexia Nervosa; Anthrax; Antiphospholipid Syndrome; Antisocial Personality Disorder; Antithrombin III Deficiency; Antley Bixler Syndrome; Apert Syndrome; Aplasia Cutis Congenita; Apnea, Infantile; Apnea, Sleep; Apraxia; Arachnoid Cysts; Arachnoiditis; Arginase Deficiency; Argininosuccinic Aciduria; Arnold-Chiari Malformation; Arteriovenous Malformation; Arteritis, Giant Cell; Arteritis, Takayasu; Arthritis, Infectious; Arthritis, Juvenile Rheumatoid; Arthritis, Psoriatic; Arthrogryposis Multiplex Congenita; Asherman's Syndrome; Aspartylglycosaminuria; Asperger's Syndrome; Aspergillosis; Astrocytoma; Astrocytoma, Malignant; Ataxia Telangiectasia; Ataxia with Vitamin E Deficiency; Ataxia, Friedreich's; Ataxia, Hereditary, Autosomal Dominant; Atrial Septal Defects; Atrioventricular Septal Defect; Attention Deficit Hyperactivity Disorder; Atypical Hemolytic Uremic Syndrome; Atypical Mole Syndrome; Autism; Autoimmune Polyendocrine Syndrome Type II; Autoimmune Thyroiditis; Babesiosis; Balantidiasis; Baller Gerold Syndrome; Balo Disease; Bannayan Riley Ruvalcaba Syndrome; Banti's Syndrome; Bardet Biedl Syndrome; Barrett Esophagus; Barth Syndrome; Bartonellosis; Bartter's Syndrome; Batten Disease; Beals Syndrome; Beckwith Wiedemann Syndrome; Behcet's Syndrome; Bejel; Bell's Palsy; Benign Essential Tremor; Bernard Soulier Syndrome; Berylliosis; Best Vitelliform Macular Dystrophy; Biliary Atresia, Extrahepatic; Binswanger's Disease; Bjornstad Syndrome; Bladder Exstrophy-Epispadias-Cloacal Exstrophy Complex; Blastomycosis; Blepharophimosis, Ptosis, Epicanthus Inversus Syndrome; Blepharospasm, Benign Essential; Bloom Syndrome; Blue Diaper Syndrome; Blue Rubber Bleb Nevus; Borjeson Syndrome; Botulism; Bowen Hutterite Syndrome; Bowen's Disease; Bowenoid Papulosis; Brachial Plexus Palsy; Brain Tumors, General; Branchio Oculo Facial Syndrome; Branchio Oto Renal Syndrome; Bronchopulmonary Dysplasia (BPD); Brown Sequard Syndrome; Brown Syndrome; Brucellosis; Bubonic Plague; Budd Chiari Syndrome; Buerger's Disease; Bulimia; Bullous Pemphigoid; Burning Mouth Syndrome; C Syndrome; CHARGE Syndrome; Campomelic Syndrome; Camurati-Engelmann Disease; Canavan Disease; Cancer, Colon; Cancer, Prostate; Cancers, Skin, General; Candidiasis; Carbamyl Phosphate Synthetase Deficiency; Carbohydrate Deficient Glycoprotein Syndrome Type Ia ; Carboxylase Deficiency, Multiple; Carcinoid Syndrome; Carcinoma, Renal Cell; Carcinoma, Squamous Cell; Cardiofaciocutaneous Syndrome; Carnitine Deficiency Syndromes; Carnitine Palmitoyltransferase Deficiency; Carnosinemia; Caroli Disease; Carpal Tunnel Syndrome; Carpenter Syndrome; Castleman's Disease; Cat Eye Syndrome; Cat Scratch Disease; Cataract Dental Syndrome; Cataracts; Catel Manzke Syndrome; Caudal Regression Syndrome;Cavernous Malformation; Cayler Syndrome; Celiac Disease; Central Core Disease; Central Hypoventilation Syndrome, Congenital; Cerebellar Agenesis; Cerebellar Degeneration, Subacute; Cerebral Palsy; Cerebro Oculo Facio Skeletal Syndrome; Cerebrocostomandibular Syndrome; Chagas Disease; Chalazion; Chandler's Syndrome; Charcot Marie Tooth Disease; Chediak Higashi Syndrome; Chiari Frommel Syndrome; Chikungunya; Chlamydia; Cholangitis, Primary Sclerosing; Cholecystitis; Cholera; Cholestasis; Chondrocalcinosis, Familial Articular; Chordoma; Chorea, Sydenham's; Choroideremia; Choroiditis, Serpiginous; Chromosome 10, Distal Trisomy 10q ; Chromosome 10, Monosomy 10p; Chromosome 11, Partial Monosomy 11q; Chromosome 11, Partial Trisomy 11q; Chromosome 13, Partial Monosomy 13q; Chromosome 14 Ring; Chromosome 14, Trisomy Mosaic; Chromosome 15 Ring; Chromosome 15, Distal Trisomy 15q; Chromosome 18 Ring; Chromosome 18, Monosomy 18p; Chromosome 18, Tetrasomy 18p; Chromosome 18q- Syndrome; Chromosome 21 Ring; Chromosome 22 Ring; Chromosome 22, Trisomy Mosaic; Chromosome 3, Monosomy 3p2; Chromosome 3, Trisomy 3q2; Chromosome 4 Ring; Chromosome 4, Monosomy 4q; Chromosome 4, Monosomy Distal 4q; Chromosome 4, Partial Trisomy Distal 4q; Chromosome 4, Trisomy 4p; Chromosome 5, Trisomy 5p; Chromosome 6 Ring; Chromosome 6, Partial Trisomy 6q; Chromosome 7, Partial Monosomy 7p; Chromosome 8, Monosomy 8p2; Chromosome 9 Ring; Chromosome 9, Partial Monosomy 9p; Chromosome 9, Tetrasomy 9p; Chromosome 9, Trisomy 9p (Multiple Variants); Chromosome 9, Trisomy Mosaic; Chronic Fatigue Syndrome; Chronic Fatigue Syndrome/Myalgic Encephalomyelitis; Chronic Inflammatory Demyelinating Polyneuropathy; Churg Strauss Syndrome; Ciguatera Fish Poisoning; Cirrhosis, Primary Biliary; Citrullinemia; Cleft Palate and Cleft Lip; Cleidocranial Dysplasia; Clubfoot; Coats' Disease; Cochin Jewish Disorder; Cockayne Syndrome; Coffin Lowry Syndrome; Coffin Siris Syndrome; Cogan Reese Syndrome; Cohen Syndrome; Colitis, Collagenous; Colitis, Ulcerative; Colorado Tick Fever; Common Variable Immunodeficiency; Condyloma; Cone Dystrophy; Congenital Fibrosis of the Extraocular Muscles; Congenital Varicella Syndrome; Conjunctivitis, Ligneous; Conn Syndrome; Conradi Hunermann Syndrome; Conversion Disorder; Cor Triatriatum; Corneal Dystrophies; Cornelia de Lange Syndrome; Corticobasal Degeneration; Costello Syndrome; Cowpox; Craniofrontonasal Dysplasia; Craniometaphyseal Dysplasia; Craniosynostosis, Primary; Creutzfeldt Jakob Disease; Cri du Chat Syndrome; Crigler Najjar Syndrome Type I; Crohn's Disease; Cronkhite-Canada Syndrome; Crouzon Syndrome; Cryoglobulinemia, Essential Mixed; Cryptococcosis; Cushing's Syndrome; Cutaneous T-Cell Lymphomas; Cutis Laxa; Cutis Marmorata Telangiectatica Congenita; Cyclic Vomiting Syndrome; Cystic Fibrosis; Cystic Hygroma; Cysticercosis; Cystinosis; Cystinuria; Cytochrome C Oxidase Deficiency; Cytomegalovirus Infection; DOOR Syndrome; Dandy Walker Malformation; De Barsy Syndrome; De Santis Cacchione Syndrome; Degos Disease; Dejerine Sottas Disease; Dengue Fever; Dentin Dysplasia, Coronal; Dentin Dysplasia, Type I; Dentinogenesis Imperfecta Type III; Depersonalization Disorder; Dercum Disease; Dermatitis Herpetiformis; Dermatitis, Atopic; Dermatitis, Contact; Dermatomyositis; Devic Disease; Dextrocardia with Situs Inversus; DiGeorge Syndrome; Diabetes Insipidus; Diabetes, Insulin Dependent; Diastrophic Dysplasia; Diencephalic Syndrome; Diffuse Idiopathic Skeletal Hyperostosis; Dilatation of the Pulmonary Artery, Idiopathic; Disaccharide Intolerance I; Diverticulitis; Diverticulosis; Down Syndrome; Dracunculosis; Drash Syndrome; Duane Syndrome; Dubin Johnson Syndrome; Dubowitz Syndrome; Duodenal Atresia or Stenosis; Dupuytren's Contracture; Dyggve Melchior Clausen Syndrome; Dysautonomia, Familial; Dyschondrosteosis; Dyskeratosis Congenita; Dyslexia; Dysplasia, Epiphysealis Hemimelica; Dysplasia, Fibrous; Dysthymia; Dystonia; Dystrophy, Asphyxiating Thoracic; Dystrophy, Myotonic; Eales Disease; Ear, Patella, Short Stature Syndrome; Ectodermal Dysplasias; Ectrodactyly Ectodermal Dysplasia Cleft Lip/Palate; Edema, Idiopathic; Ehlers Danlos Syndrome; Eisenmenger Syndrome; Elephantiasis; Ellis Van Creveld Syndrome; Emphysema, Congenital Lobar; Empty Sella Syndrome; Encephalitis, Herpes Simplex; Encephalitis, Japanese; Encephalitis, Rasmussen's; Encephalocele; Endocardial Fibroelastosis; Endocarditis, Infective; Endometriosis; Endomyocardial Fibrosis; Enterobiasis; Eosinophilia Myalgia; Eosinophilic Fasciitis; Epidermal Nevus Syndrome; Epidermolysis Bullosa; Epidermolytic Hyperkeratosis; Epididymitis; Epilepsy; Epitheliopathy, Acute Posterior Multifocal Placoid Pigment; Erdheim Chester Disease; Erysipelas; Erythema Multiforme; Erythroderma desquamativa of Leiner; Erythrokeratodermia with Ataxia; Erythromelalgia; Erythropoietic Protoporphyria; Esophageal Atresia and/or Tracheoesophageal Fistula; Essential Iris Atrophy; Ewing's Sarcoma; Exostoses, Multiple; FG Syndrome; Fabry Disease; Facioscapulohumeral Muscular Dystrophy; Factor IX Deficiency; Factor XIII Deficiency; Fahr's Disease; Familial Adenomatous Polyposis; Familial Eosinophilic Cellulitis; Familial Juvenile Hyperuricemic Nephropathy; Familial Lipoprotein Lipase Deficiency; Farber's Disease; Fascioliasis; Felty Syndrome; Femoral Facial Syndrome; Fetal Alcohol Syndrome; Fetal Hydantoin Syndrome; Fetal Retinoid Syndrome; Fetal Valproate Syndrome; Fiber Type Disproportion, Congenital; Fibrodysplasia Ossificans Progressiva (FOP); Fibromatosis, Congenital Generalized; Fibromyalgia; Filariasis; Filippi Syndrome; Fitz Hugh Curtis Syndrome; Floating Harbor Syndrome; Focal Dermal Hypoplasia; Forbes Disease; Formaldehyde Poisoning; Fountain Syndrome; Fournier Gangrene; Fox Fordyce Disease; Fragile X Syndrome; Fraser Syndrome; Freeman Sheldon Syndrome; Frey's Syndrome; Froelich's Syndrome; Frontofacionasal Dysplasia; Frontonasal Dysplasia; Fructose Intolerance, Hereditary; Fructosuria; Fryns Syndrome; Fukuyama Type Congenital Muscular Dystrophy; Galactosemia; Galloway Mowat Syndrome; Gardner Syndrome; Gastritis, Chronic, Erosive; Gastritis, Giant Hypertrophic; Gastroenteritis, Eosinophilic; Gastroesophageal Reflux; Gastrointestinal Stromal Tumors; Gastroschisis; Gaucher Disease; Gerstmann Syndrome; Gianotti Crosti Syndrome; Giant Cell Myocarditis; Giardiasis; Gilbert Syndrome; Glanzmann Thrombasthenia; Glioblastoma Multiforme; Glucose Galactose Malabsorption; Glucose-6-Phosphate Dehydrogenase Deficiency; Glutaricaciduria I; Glutaricaciduria II; Glycogen Storage Disease Type V; Glycogen Storage Disease VIII; Goldenhar Syndrome (Oculo Auriculo Vertebral Spectrum); Goodman Syndrome; Goodpasture Syndrome; Gordon Syndrome; Gorham's Disease; Gorlin Chaudhry Moss Syndrome; Gottron Syndrome; Graft versus Host Disease; Granuloma Annulare; Granulomatosis, Lymphomatoid; Granulomatous Disease, Chronic; Graves' Disease; Greig Cephalopolysyndactyly Syndrome; Grover's Disease; Growth Delay, Constitutional; Growth Hormone Deficiency; Guillain Barre Syndrome; Hageman Factor Deficiency; Hajdu Cheney Syndrome; Hallermann Streiff syndrome; Hand Foot Mouth Syndrome; Hanhart Syndrome; Hantavirus Pulmonary Syndrome; Hartnup Disease; Hay-Wells Syndrome; Headache, Cluster; Heart Block, Congenital; Heavy Metal Poisoning; Hemangioma Thrombocytopenia Syndrome; Hematuria, Benign, Familial; Hemochromatosis, Hereditary; Hemoglobinuria, Paroxysmal Cold; Hemoglobinuria, Paroxysmal Nocturnal; Hemolytic Uremic Syndrome; Hemophilia; Hemorrhagic Telangiectasia, Hereditary; Hepatic Fibrosis, Congenital; Hepatitis B; Hepatitis C; Hepatitis, Neonatal; Hepatorenal Syndrome; Hermansky Pudlak Syndrome; Hermaphroditism, True; Herpes, Neonatal; Hers Disease; Hiccups, Chronic; Hidradenitis Suppurativa; Hirschsprung's Disease; Histidinemia; Hodgkin's Disease; Holoprosencephaly; Holt Oram Syndrome; Homocystinuria; Horner's Syndrome; Human Granulocytic Ehrlichiosis (HGE); Human Monocytic Ehrlichiosis (HME); Hunter Syndrome; Huntington's Disease; Hydranencephaly; Hydrocephalus; Hyper IgM Syndrome; Hypercholesterolemia; Hyperemesis Gravidarum; Hyperexplexia; Hyperhidrosis, Primary; Hyperkalemia; Hyperlipoproteinemia Type III; Hyperlipoproteinemia Type IV; Hyperostosis Frontalis Interna; Hyperoxaluria, Primary (Type I); Hyperprolinemia Type I; Hyperprolinemia Type II; Hyperthermia; Hypochondroplasia; Hypoglycemia; Hypohidrotic Ectodermal Dysplasia; Hypokalemia; Hypomelanosis of Ito; Hypoparathyroidism; Hypophosphatasia; Hypophosphatemia, Familial; Hypoplastic Left Heart Syndrome; Hypotension, Orthostatic; Hypothyroidism; Hypotonia, Benign Congenital; I Cell Disease; IRF6-Related Disorders; Ichthyosis; Ichthyosis Hystrix, Curth Macklin Type; Ichthyosis Vulgaris; Ichthyosis, CHILD Syndrome; Ichthyosis, Chanarin Dorfman Syndrome; Ichthyosis, Erythrokeratodermia Progressiva Symmetrica; Ichthyosis, Erythrokeratodermia Variabilis; Ichthyosis, Erythrokeratolysis Hiemalis; Ichthyosis, Harlequin Type; Ichthyosis, Keratosis Follicularis Spinulosa Decalvans; Ichthyosis, Lamellar; Ichthyosis, Netherton Syndrome; Ichthyosis, Sjogren Larsson Syndrome; Ichthyosis, Trichothiodystrophy; Ichthyosis, X Linked; Idiopathic Pulmonary Fibrosis; IgA Nephropathy; Imperforate Anus; Incontinentia Pigmenti; Interstitial Cystitis; Intestinal Pseudoobstruction; Irritable Bowel Syndrome; Ivemark Syndrome; Jackson Weiss Syndrome; Jansen Type Metaphyseal Chondrodysplasia; Jarcho Levin Syndrome; Jejunal Atresia; Jervell and Lange-Nielsen Syndrome; Job Syndrome; Johanson Blizzard Syndrome; Joubert Syndrome; Jumping Frenchmen of Maine; KBG Syndrome; Kabuki Make-up Syndrome; Kallmann Syndrome; Kartagener Syndrome; Kawasaki Disease; Kearns Sayre Syndrome; Kennedy Disease; Kenny Caffey Syndrome; Keratitis Ichthyosis Deafness Syndrome; Keratoconjunctivitis, Vernal; Keratoconus; Keratomalacia; Keratosis Follicularis; Keratosis, Seborrheic; Kernicterus; Kienbock Disease; Kikuchi's Disease; Kleine Levin Syndrome; Klinefelter Syndrome; Klippel Trenaunay Syndrome; Klippel-Feil Syndrome; Kluver Bucy Syndrome; Kniest Dysplasia; Kohler Disease; Kufs Disease; Kugelberg Welander Syndrome; L1 Syndrome; LADD Syndrome; LEOPARD Syndrome; Laband Syndrome; Lactose Intolerance; Lambert-Eaton Myasthenic Syndrome; Landau Kleffner Syndrome; Langerhans Cell Histiocytosis; Laron Syndrome; Larsen Syndrome; Laurence Moon Syndrome; Leber Hereditary Optic Neuropathy; Leber's Congenital Amaurosis; Legg Calve Perthes Disease; Legionnaires' Disease; Leigh's Disease; Lennox Gastaut Syndrome; Lenz Microphthalmia Syndrome; Leprechaunism; Leprosy; Leptospirosis; Leri Pleonosteosis; Lesch Nyhan Syndrome; Leukemia, Chronic Lymphocytic; Leukemia, Chronic Myelogenous; Leukemia, Hairy Cell; Leukodystrophy; Leukodystrophy, Krabbe's; Leukodystrophy, Metachromatic; Lichen Planus; Lichen Sclerosus; Lipodystrophy; Lissencephaly; Listeriosis; Locked In Syndrome; Loken Senior Syndrome; Lowe Syndrome; Lupus; Lyme Disease; Lymphadenopathy, Angioimmunoblastic with Dysproteinemia; Lymphangioleiomyomatosis; Lymphatic Malformations; Lymphedema, Hereditary; Lymphocytic Infiltrate of Jessner; Lymphoma, Gastric, Non Hodgkins Type; Lynch Syndromes; Lysosomal Storage Disorders; MELAS Syndrome; MERRF Syndrome; MURCS Association; Machado-Joseph Disease; Macroglossia; Macular Degeneration; Madelung's Disease; Maffucci Syndrome; Mal de Debarquement; Malaria; Malignant Hyperthermia; Mallory Weiss Syndrome; Manic Depression, Bipolar; Mantle Cell Lymphoma; Maple Syrup Urine Disease; Marcus Gunn Phenomenon; Marden Walker Syndrome; Marfan Syndrome; Marinesco Sjogren Syndrome; Maroteaux Lamy Syndrome; Marshall Smith Syndrome; Marshall Syndrome; Mastocytosis; Maxillofacial Dysostosis; Maxillonasal Dysplasia, Binder Type; May Hegglin Anomaly; McCune Albright Syndrome; McKusick Type Metaphyseal Chondrodysplasia; Measles; Meckel Syndrome; Mediterranean Fever, Familial; Medium Chain Acyl CoA Dehydrogenase Deficiency; Medullary Cystic Kidney Disease/Nephronophthisis; Medullary Sponge Kidney; Medulloblastoma; Megalocornea Mental Retardation Syndrome; Meige Syndrome; Melanoma, Malignant; Meleda Disease; Melkersson Rosenthal Syndrome; Melnick Needles Syndrome; Membranoproliferative Glomerulonephritis Type II; Meniere Disease; Meningioma; Meningitis; Meningitis, Bacterial; Meningitis, Meningococcal; Meningitis, Tuberculous; Meningococcemia; Menkes Disease; Mesenteritis, Retractile; Mesothelioma; Metaphyseal Chondrodysplasia, Schmid Type; Metatropic Dysplasia I; Microvillus Inclusion Disease; Mikulicz Syndrome; Miller Syndrome; Mitral Valve Prolapse Syndrome; Mixed Connective Tissue Disease (MCTD); Moebius Syndrome; Monilethrix; Morquio Syndrome; Motor Neuron Disease; Mountain Sickness, Acute; Mowat-Wilson Syndrome; Moyamoya Syndrome; Mucha Habermann Disease; Mucolipidosis IV; Mucopolysaccharidoses; Mucopolysaccharidosis Type I; Mucopolysaccharidosis Type III; Mucous Membrane Pemphigoid; Mulibrey Nanism Syndrome (Perheentupa Syndrome); Mullerian Aplasia; Multiple Epiphyseal Dysplasia; Multiple Sclerosis; Multiple Sulfatase Deficiency; Multiple System Atrophy; Mulvihill Smith Syndrome; Mumps; Muscular Dystrophy, Becker; Muscular Dystrophy, Duchenne; Muscular Dystrophy, Emery Dreifuss; Muscular Dystrophy, Limb Girdle; Muscular Dystrophy, Oculo Gastrointestinal; Mutism, Selective; Myasthenia Gravis; Mycosis Fungoides; Myelodysplastic Syndromes; Myelofibrosis, Idiopathic; Myeloma, Multiple; Myhre Syndrome; Myoclonus, General; Myopathy, Congenital, Batten Turner Type; Myopathy, Desmin Storage; Myopathy, Scapuloperoneal; Myositis, Inclusion Body; Myotonia Congenita; Myotubular Myopathy; N-Acetyl Glutamate Synthetase Deficiency; Nager Syndrome; Nail Patella Syndrome; Narcolepsy; Nelson Syndrome; Nemaline Myopathy; Neonatal Lupus; Neu Laxova Syndrome; Neurasthenia; Neuroacanthocytosis; Neurodegeneration with Brain Iron Accumulation Type 1; Neurofibromatosis Type 1 (NF-1); Neurofibromatosis Type 2 (NF-2); Neuroleptic Malignant Syndrome; Neuromyotonia; Neuropathy, Ataxia and Retinitis Pigmentosa; Neuropathy, Congenital Hypomyelination; Neuropathy, Giant Axonal; Neuropathy, Hereditary Sensory, Type I; Neuropathy, Hereditary Sensory, Type II; Neuropathy, Hereditary Sensory, Type IV; Neuropathy, Peripheral; Neutropenia, Cyclic; Neutropenia, Severe Chronic; Nevoid Basal Cell Carcinoma Syndrome; Nezelof's Syndrome; Niemann Pick Disease; Nocardiosis; Nonketotic Hyperglycinemia; Noonan Syndrome; Norrie Disease; Nystagmus, Benign Paroxysmal Positional;Obsessive Compulsive Disorder; Ochoa Syndrome; Ocular Motor Apraxia, Cogan Type; Oculo-Dento-Digital Dysplasia; Oculocerebral Syndrome with Hypopigmentation; Oculocerebrocutaneous Syndrome; Olivopontocerebellar Atrophy, Hereditary; Ollier Disease; Opitz G/BBB Syndrome; Opportunistic Infections; Opsoclonus-Myoclonus Syndrome; Oral Facial Digital Syndrome; Organic Personality Syndrome; Ornithine Transcarbamylase Deficiency; Orocraniodigital Syndrome; Osgood Schlatter Condition; Osteogenesis Imperfecta; Osteomyelitis; Osteonecrosis; Osteopetrosis; Otopalatodigital Syndrome Type I and II; PEPCK Deficiency, Mitochondrial; POEMS Syndrome; Pachydermoperiostosis; Pachyonychia Congenita; Paget's Disease; Paget's Disease of the Breast; Pallister Hall Syndrome; Pallister Killian Mosaic Syndrome; Pallister W Syndrome; Pancreatic Islet Cell Tumor; Panic Anxiety Syndrome; Panniculitis, Idiopathic Nodular; Papillitis; Papillon Lefevre Syndrome; Paracoccidioidomycosis; Paramyotonia Congenita; Paraplegia, Hereditary Spastic; Parkinson's Disease; Parry Romberg Syndrome; Pars Planitis; Parsonage Turner Syndrome; Patulous Eustachian Tube; Pediatric Cardiomyopathy; Peeling Skin Syndrome; Pelizaeus Merzbacher Brain Sclerosis; Pemphigus; Penta X Syndrome; Pentalogy of Cantrell; Perisylvian Syndrome, Congenital Bilateral; Perniosis; Pertussis; Peutz Jeghers Syndrome; Peyronie Disease; Pfeiffer Syndrome Type I; Phelan-McDermid Syndrome; Phenylketonuria; Pheochromocytoma; Phocomelia Syndrome; Phosphoglycerate Kinase Deficiency; Pica; Pick's Disease; Pierre Robin Sequence; Pineal Cysts, Symptomatic; Pinta; Pityriasis Rubra Pilaris; Pleuropulmonary Blastoma; Pneumonia, Eosinophilic; Pneumonia, Interstitial; Poland Syndrome; Polyarteritis Nodosa; Polychondritis; Polycystic Kidney Diseases; Polycystic Liver Disease; Polycystic Ovary Syndrome; Polycythemia Vera; Polyglucosan Body Disease, Adult; Polymorphous Low-Grade Adenocarcinoma; Polymyalgia Rheumatica; Polymyositis; Pompe Disease; Porphyria; Porphyria Cutanea Tarda; Porphyria, ALA-D; Porphyria, Acute Intermittent; Porphyria, Congenital Erythropoietic; Porphyria, Hereditary Coproporphyria; Porphyria, Variegate; Post Polio Syndrome; Posterior Uveitis; Prader Willi Syndrome; Precocious Puberty; Primary Lateral Sclerosis; Primary Orthostatic Tremor; Proctitis; Progeria, Hutchinson Gilford; Progressive Myoclonus Epilepsy; Progressive Osseous Heteroplasia (POH); Progressive Supranuclear Palsy; Prostatitis; Proteus Syndrome; Prune Belly Syndrome; Pseudo Hurler Polydystrophy; Pseudoachondroplastic Dysplasia; Pseudocholinesterase Deficiency; Pseudohypoparathyroidism; Pseudomyxoma Peritonei; Pseudotumor Cerebri; Pseudoxanthoma Elasticum (PXE); Psittacosis; Psoriasis; Pterygium Syndrome, Multiple; Pulmonary Alveolar Proteinosis; Pulmonary Hypertension, Primary; Pulmonary Hypertension, Secondary; Pure Red Cell Aplasia, Acquired; Purpura, Henoch-Schonlein; Purpura, Idiopathic Thrombocytopenic; Purpura, Thrombotic Thrombocytopenic; Pyknodysostosis; Pyoderma Gangrenosum; Pyridoxine-Dependent Seizures; Pyruvate Carboxylase Deficiency; Pyruvate Dehydrogenase Deficiency; Pyruvate Kinase Deficiency; Q Fever; Rabies; Rabson-Mendenhall Syndrome; Radiation Syndromes; Ramsay-Hunt Syndrome; Rapp Hodgkin Syndrome; Raynaud's Disease and Phenomenon; Recurrent Respiratory Papillomatosis; Reflex Sympathetic Dystrophy Syndrome; Refsum Disease; Reiter's Syndrome; Renal Agenesis, Bilateral; Renal Glycosuria; Respiratory Distress Syndrome, Infant; Restless Legs Syndrome; Retinitis Pigmentosa; Retinoblastoma; Retinopathy of Prematurity; Retinopathy, Arteriosclerotic; Retinopathy, Diabetic; Retinopathy, Hypertensive; Retinoschisis; Retroperitoneal Fibrosis; Rett Syndrome; Reye Syndrome; Rh Disease; Rheumatic Fever; Rickets, Vitamin D Deficiency; Rieger Syndrome; Roberts Syndrome; Robinow Syndrome; Rocky Mountain Spotted Fever; Romano Ward Syndrome; Rosai-Dorfman Disease; Rosenberg Chutorian Syndrome; Roseola Infantum; Rothmund Thomson Syndrome; Roussy Levy Syndrome; Rubella; Rubella, Congenital; Rubinstein Taybi Syndrome; Russell Silver Syndrome (RSS); Ruvalcaba Syndrome; SHORT Syndrome; Saethre Chotzen Syndrome; Sakati Syndrome; Sandhoff Disease; Santavuori Disease; Sarcoidosis; Schindler Disease; Schinzel Giedion Syndrome; Schinzel Syndrome; Schwartz Jampel Syndrome; Scleroderma; Scott Craniodigital Syndrome; Seckel Syndrome; Seitelberger Disease (Infantile Neuroaxonal Dystrophy); Sennetsu Fever; Septooptic Dysplasia; Setleis Syndrome; Severe Combined Immunodeficiency; Sheehan Syndrome; Short Chain Acyl CoA Dehydrogenase Deficiency (SCAD); Shwachman Syndrome; Sialadenitis; Sialidosis; Sickle Cell Disease; Simian B Virus Infection; Simpson Dysmorphia Syndrome; Singleton Merten Syndrome; Sinonasal Undifferentiated Carcinoma; Sirenomelia Sequence; Sjogren Syndrome; Sly Syndrome; Smallpox; Smith Lemli Opitz Syndrome; Smith Magenis Syndrome; Sneddon Syndrome; Sotos Syndrome; Spasmodic Dysphonia; Spasmodic Torticollis; Spina Bifida; Spinal Muscular Atrophy; Split Hand/Split Foot Malformation; Spondyloepiphyseal Dysplasia Tarda; Spondyloepiphyseal Dysplasia, Congenital; Sprengel Deformity; Stenosis, Spinal; Stevens Johnson Syndrome; Stickler Syndrome; Stiff Person Syndrome; Streptococcus, Group B; Sturge Weber Syndrome; Stuve-Wiedemann Syndrome; Subacute Sclerosing Panencephalitis; Succinic Semialdehyde Dehydrogenase Deficiency; Sudden Infant Death Syndrome; Summitt Syndrome; Susac Syndrome; Sutton Disease II; Sweet Syndrome; Syphilis, Acquired; Syphilis, Congenital; Syringobulbia; Syringomyelia; TORCH Syndrome; Tangier Disease; Tardive Dyskinesia ; Tarsal Tunnel Syndrome; Tarui Disease; Tay Sachs Disease; Telecanthus with Associated Abnormalities; Temporomandibular Joint Dysfunction (TMJ); Tethered Spinal Cord Syndrome; Tetrahydrobiopterin Deficiency; Tetralogy of Fallot; Thalamic Syndrome (Dejerine Roussy); Thalassemia Major; Thalassemia Minor; Three M Syndrome; Thrombocythemia, Essential; Thrombocytopenia Absent Radius Syndrome; Thrombocytopenia, Essential; Tietze Syndrome; Timothy Syndrome; Tinnitus; Tolosa Hunt Syndrome; Tongue Carcinoma; Tongue, Fissured; Tongue, Geographic; Tongue, Hairy; Tooth and Nail Syndrome; Tourette Syndrome; Townes Brocks Syndrome; Toxic Epidermal Necrolysis; Toxic Shock Syndrome; Toxocariasis; Toxoplasmosis; Transverse Myelitis; Treacher Collins Syndrome; Tricho Dento Osseous Syndrome; Trichorhinophalangeal Syndrome Type I; Trichorhinophalangeal Syndrome Type III; Trichotillomania; Trigeminal Neuralgia (Tic Douloureux); Trimethylaminuria; Triplo X Syndrome; Triploid Syndrome; Trismus Pseudocamptodactyly Syndrome; Trisomy; Trisomy 13 Syndrome; Trisomy 18 Syndrome; Tropical Sprue; Truncus Arteriosus; Tuberculosis; Tuberous Sclerosis; Tularemia; Turcot Syndrome; Turner Syndrome; Twin Twin Transfusion Syndrome; Typhoid; Tyrosinemia, Hereditary; Urticaria Pigmentosa; Urticaria, Cholinergic; Urticaria, Cold; Urticaria, Papular; Urticaria, Physical; Usher Syndrome; VACTERL Association; VACTERL with Hydrocephalus; Valinemia; Varicella Zoster; Vascular Malformations of the Brain; Vasculitis; Vasculitis, Cutaneous Necrotizing; Velocardiofacial Syndrome; Ventricular Septal Defects; Very Long Chain Acyl CoA Dehydrogenase Deficiency (LCAD); Vitamin B12 Deficiency; Vitiligo; Vogt Koyanagi Harada Syndrome; Von Gierke Disease; Von Hippel Lindau Disease; Von Willebrand Disease; Vulvovaginitis; WAGR Syndrome; Waardenburg Syndrome; Waldenstrom's Macroglobulinemia; Waldmann Disease; Walker Warburg Syndrome; Wandering Spleen; Weaver Syndrome; Wegener's Granulomatosis; Weil Syndrome; Weill Marchesani Syndrome; Weismann Netter Stuhl Syndrome; Werdnig Hoffman Disease; Werner Syndrome; Wernicke-Korsakoff Syndrome; West Nile Encephalitis; West Syndrome; Whipple Disease; Wieacker Syndrome; Wiedemann Rautenstrauch Syndrome; Wildervanck Syndrome; Williams Syndrome; Wilms' Tumor; Wilson's Disease; Winchester Syndrome; Wiskott Aldrich Syndrome; Wolf Hirschhorn Syndrome; Wolff Parkinson White Syndrome; Wolfram Syndrome; Wyburn Mason Syndrome; X linked Juvenile Retinoschisis; X linked Lymphoproliferative Syndrome; XYY Syndrome; Xeroderma Pigmentosum; Yaws; Yellow Fever; Yellow Nail Syndrome; Yunis Varon Syndrome; Zellweger Syndrome; Zollinger Ellison Syndrome; sanitary preparations for medical use; chemical preparations for use in medicine; dietetic foods adapted for medical use; disinfectants for medical use; preparations for destroying vermin; fungicides for medical use; herbicides; diagnostic preparations for clinical or medical use; diagnostic preparations for veterinary use; pharmaceutical preparations, namely contrast agents for radiography, x-ray radiography, computer tomography, magnetic resonance imaging, magnetic resonance tomography; medical preparations for treatment or prevention of diseases of the mouth; and medical preparations for treatment or prevention of diseases of the skin
GS0351	Business consulting and information services for scientific projects in the field of medicine, pharmacy, biology, and chemistry or medicine-technology; assistance, advisory services and consultancy with regard to business planning, business analysis, business management, and business organization for scientific projects in the field of medicine, pharmacy, biology, and chemistry or medicine-technology; business acquisition and merger consultation in the field of medicine, pharmacy, biology, and chemistry or medicine-technology
GS0421	Commissioned development of pharmaceutical preparations; conducting clinical trials for medical and scientific research; conducting early evaluations in the field of new pharmaceuticals, scientific research consulting, namely commissioned assessment of scientific projects, and commissioned assessment of clinical studies and clinical trials; product development for others in the field of medicine, pharmacy, biology, chemistry and medicine-technology; medical and scientific development and research services in the field of medical, biochemical, pharmaceutical and medicine-technological research; product development for others, namely development of pharmaceutical preparations and medicines; pharmaceutical drug development services; product development consulting, namely pharmaceutical product evaluation; pharmaceutical research and development; pharmaceutical research services; providing information relating to legal affairs
GS0441	Medical services

PROSECUTION HISTORY
Date	Description	Type	Code
02/02/2009	ABANDONMENT NOTICE MAILED - NO USE STATEMENT FILED	O - Outgoing Correspondence	MAB6 - ABANDONMENT NOTICE MAILED - NO USE STATEMENT FILED
02/02/2009	ABANDONMENT - NO USE STATEMENT FILED	S	ABN6 - ABANDONMENT - NO USE STATEMENT FILED
07/10/2008	EXTENSION 3 GRANTED	S	EX3G - EXTENSION 3 GRANTED
07/01/2008	EXTENSION 3 FILED	S	EXT3 - EXTENSION 3 FILED
07/01/2008	TEAS EXTENSION RECEIVED	I - Incoming Correspondence	EEXT - TEAS EXTENSION RECEIVED
12/31/2007	EXTENSION 2 GRANTED	S	EX2G - EXTENSION 2 GRANTED
12/31/2007	EXTENSION 2 FILED	S	EXT2 - EXTENSION 2 FILED
12/31/2007	TEAS EXTENSION RECEIVED	I - Incoming Correspondence	EEXT - TEAS EXTENSION RECEIVED
09/11/2007	EXTENSION 1 GRANTED	S	EX1G - EXTENSION 1 GRANTED
06/29/2007	EXTENSION 1 FILED	S	EXT1 - EXTENSION 1 FILED
06/29/2007	TEAS EXTENSION RECEIVED	I - Incoming Correspondence	EEXT - TEAS EXTENSION RECEIVED
01/02/2007	NOA MAILED - SOU REQUIRED FROM APPLICANT	O - Outgoing Correspondence	NOAM - NOTICE OF ALLOWANCE-MAILED
10/10/2006	PUBLISHED FOR OPPOSITION	A - Allowance for Publication	PUBO - PUBLISHED FOR OPPOSITION
09/20/2006	NOTICE OF PUBLICATION	O - Outgoing Correspondence	NPUB - NOTICE OF PUBLICATION
08/23/2006	LAW OFFICE PUBLICATION REVIEW COMPLETED	O - Outgoing Correspondence	PREV - LAW OFFICE PUBLICATION REVIEW COMPLETED
08/18/2006	ASSIGNED TO LIE	A - Allowance for Publication	ALIE - ASSIGNED TO LIE
08/17/2006	APPROVED FOR PUB - PRINCIPAL REGISTER	P	CNSA - APPROVED FOR PUB - PRINCIPAL REGISTER
08/08/2006	TEAS/EMAIL CORRESPONDENCE ENTERED	I - Incoming Correspondence	TEME - TEAS/EMAIL CORRESPONDENCE ENTERED
06/29/2006	CORRESPONDENCE RECEIVED IN LAW OFFICE	I - Incoming Correspondence	CRFA - CORRESPONDENCE RECEIVED IN LAW OFFICE
06/29/2006	TEAS RESPONSE TO OFFICE ACTION RECEIVED	I - Incoming Correspondence	TROA - TEAS RESPONSE TO OFFICE ACTION RECEIVED
01/03/2006	NON-FINAL ACTION E-MAILED	F - First Action	GNRT - NON-FINAL ACTION E-MAILED
01/03/2006	NON-FINAL ACTION WRITTEN	R - Renewal	CNRT - NON-FINAL ACTION WRITTEN
12/28/2005	ASSIGNED TO EXAMINER	D - Assigned to Examiner	DOCK - ASSIGNED TO EXAMINER
06/13/2005	NEW APPLICATION ENTERED IN TRAM	I - Incoming Correspondence	NWAP - NEW APPLICATION ENTERED IN TRAM

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