AT First Diagnostic Ltd

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Web: http://www.atfirstdiagnostic.com
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Address: Atlantic Research & Development Park, Princeton, New Jersey 11791, USA
Phone: +1-(516)-776-9262 | Fax: +1-(516)-776-9264 | Map/Directions >>
 
 

Profile: AT First Diagnostic Ltd specializes in the development and marketing of quality rapid diagnostics. We are accredited with ISO 9001 certification. We use a new patent pending lateral flow technology for point-of-care testing. Our product line includes panel multi-drug kit, rapid urinalysis reagent strips, FSH Rapid Urine Test, LH ovulation rapid test and cardiac TnI rapid test. Our FirstVue™ malaria Pf-Pv test kit is used for the rapid detection of circulating plasmodium falciparum. Our diagnostic chlamydia test kit is used for detecting chlamydia trachomatis antibodies for both women and men. We also offer methamphetamine rapid screen, pregnancy midstream test device and syphilis rapid test products.

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• 10-Panel Multi-Drug Kit
• 3 Line Malaria Rapid Test
• 5-Panel Multi-Drug Rapid Home Kit
• Amphetamine Card Test
• Antibody Detection Candida Species (FDA Code: LSG / 866.3165)
• Cancer Marker Tests
• Cardiac TnI Rapid Test
• CEA Rapid Test
• Chlamydia and Gonorrhea Tests
• Chlamydia Rapid Test
• Cocaine (COC) Rapid Home Kit
• Cocaine Card Test
• Culture Media Quality Control Kit (FDA Code: JTR / 866.2480)
A quality control kit for culture media is a device that consists of paper discs (or other suitable materials), each impregnated with a specified, freeze-dried, viable microorganism, intended for medical purposes to determine if a given culture medium is able to support the growth of that microorganism. The device aids in the diagnosis of disease caused by pathogenic microorganisms and also provides epidemiological information on these diseases.
• Fertility Tests
• FSH Rapid Urine Test
• Gonorrhea Rapid Test
• Gonorrhea Test Kits
• Hepatitis B Panel Test
• Hepatitis C Antibodies (HCV) Rapid Test Kit
• Hepatitis Disease Surface Antigen (HBsAg) Test Kits
• HIV-1-2-3 Line Rapid Test
• Home pregnancy test kits, Hcg
• Influenza Virus CF Antigen (FDA Code: GNX / 866.3330)
Influenza virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to influenza in serum. The identification aids in the diagnosis of influenza (flu) and provides epidemiological information on influenza. Influenza is an acute respiratory tract disease, which is often epidemic.
• Methamphetamine Test Strip
• Mumps Virus Enzyme Linked Immunoabsorbent Assay (FDA Code: LJY / 866.3380)
Mumps virus serological reagents consist of antigens and antisera used in serological tests to identify antibodies to mumps virus in serum. Additionally, some of these reagents consist of antisera conjugated with a fluorescent dye (immunofluorescent reagents) used in serological tests to identify mumps viruses from tissue culture isolates derived from clinical specimens. The identification aids in the diagnosis of mumps and provides epidemiological information on mumps. Mumps is an acute contagious disease, particularly in children, characterized by an enlargement of one or both of the parotid glands (glands situated near the ear), although other organs may also be involved.
• Neisseria Controls (FDA Code: LSC / 866.2660)
A microorganism differentiation and identification device is a device intended for medical purposes that consists of one or more components, such as differential culture media, biochemical reagents, and paper discs or paper strips impregnated with test reagents, that are usually contained in individual compartments and used to differentiate and identify selected microorganisms. The device aids in the diagnosis of disease.
• Neisseria Gonorrhoeae Biochemical Reagent Test (FDA Code: LTS / 866.2660)
• Neisseria Gonorrhoeae Identification Kit (FDA Code: JSX / 866.2660)
• Opiates-Morphine-Heroin (MOP) Rapid Test Kit
• Over The Counter Follicle Stimulating Hormone (Fsh) Test (FDA Code: NGA / 862.1300)
A follicle-stimulating hormone test system is a device intended to measure follicle-stimulating hormone (FSH) in plasma, serum, and urine. FSH measurements are used in the diagnosis and treatment of pituitary gland and gonadal disorders.
• Over The Counter Luteinizing Hormone (Lh) Test (FDA Code: NGE / 862.1485)
A luteinizing hormone test system is a device intended to measure luteinizing hormone in serum and urine. Luteinizing hormone measurements are used in the diagnosis and treatment of gonadal dysfunction.
• Ovulation (Luteinizing Hormone) Test Kits
• Ovulation Test
• PSA Rapid Test
• Quality Control Kits (FDA Code: JTR / 866.2480)
• Rapid H. pylori Antibody (IgM/IgG/IgA) Test kits
• Rapid HIV-1 Antibody Test Kit
• Rotavirus Enzyme Linked Immunoabsorbent Assay (FDA Code: LIQ / 866.3405)
Poliovirus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to poliovirus in serum. Additionally, some of these reagents consist of poliovirus antisera conjugated with a fluorescent dye (immunofluorescent reagents) used to identify polioviruses from clinical specimens or from tissue culture isolates derived from clinical specimens. The identification aids in the diagnosis of poliomyelitis (polio) and provides epidemiological information on this disease. Poliomyelitis is an acute infectious disease which in its serious form affects the central nervous system resulting in atrophy (wasting away) of groups of muscles, ending in contraction and permanent deformity.
• Rubeola Enzyme Linked Immunoabsorbent Assay (FDA Code: LJB / 866.3520)
Rubeola (measles) virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to rubeola virus in serum. The identification aids in the diagnosis of measles and provides epidemiological information on the disease. Measles is an acute, highly infectious disease of the respiratory and reticuloendothelial tissues, particularly in children, characterized by a confluent and blotchy rash.
• Salmonella Spp Antigen (FDA Code: GRL / 866.3550)
• Strep A Rapid Test
• Streptococcus Spp Antigen (FDA Code: GTY / 866.3740)
• Streptococcus Spp Groups Fluorescent Antiserum (FDA Code: GTX / 866.3740)
• Syphilis Rapid Test
• Trichomonas Screening Kit (FDA Code: JWZ / 866.2660)
• Urinalysis Reagents & Test Strips
• Urinalysis Strips
• Urine Leukocyte Test (FDA Code: LJX / 864.7675)
A leukocyte peroxidase test is a device used to distinguish certain myeloid cells derived from the bone marrow, i.e., neutrophils, eosinophils, and monocytes, from lymphoid cells of the lymphatic system and erythroid cells of the red blood cell series on the basis of their peroxidase activity as evidenced by staining. The results of this test are used in the differential diagnosis of the leukemias.
• Urine Screening Kit (FDA Code: JXA / 866.2660)
• Vibrio Cholerae Antiserum (FDA Code: GSQ / 866.3930)

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