Address: P.O. Box 218, Somerset, New Jersey 08875-0218, USA
Phone: +1-(800)-526-2125 | Fax: +1-(732)-246-0570 | Map/Directions >>

Profile: Lifesign is a medical diagnostic company that specializes in point of care testing products. Our line of products is used for the detection of medical conditions and illnesses that include infectious disease, women's health, abused drugs & cardiac markers. Our configurable electronic real-time assessment system (CERTAS) is a desktop windows program that allows researchers and clinicians to construct questionnaires of any type using a drag & drop graphical interface that gives branching capabilities.

The company was founded in 1998, has revenues of USD 5-10 Million, has ~30 employees and is ISO 9001 certified.

FDA Registration Number: 2249224

44 Products/Services (Click for related suppliers)  
• Blood Banking, Platelet Incubators
• Cardiac Controls Set
• Co2 Water Jacketed Incubators
• Coagglutinin Test Kit
• Controls
• Drugs of Abuse Test Systems (FDA Code: MGX)
• E.Coli Testing
• Enzyme Immunoassay Test
• Fertility Monitors, Pregnancy Test Kits
• General Diagnostic Supplies
• General Diagnostics
• General Examination Supplies
• General Medical Supplies
• Home pregnancy test kits, Hcg
• Incubators
• Incubators and Shakers, Multi-Tier Shakers
• Incubators and Shakers, Rocking Shakers
• Incubators and Shakers, Rotating Tube Shakers
• Infectious Disease Exams
• Infectious Disease Testing, Rotavirus Test Kits
• Infectious Mononucleosis Radioimmunoassay Test
• Laboratory cooled incubators
• Medical Co2 Incubators
• Microbiology Kit
• Microplate Incubators and Shakers
• Mono Testing
• Neonatal Incubators (FDA Code: FMZ / 880.5400)
A neonatal incubator is a device consisting of a rigid boxlike enclosure in which an infant may be kept in a controlled environment for medical care. The device may include an AC-powered heater, a fan to circulate the warmed air, a container for water to add humidity, a control valve through which oxygen may be added, and access ports for nursing care.
• Platelet Agitators, Platelet Incubators
• Portable Test Tube Incubator
• Pregnancy Kits
• Pregnancy Test Kit
• Rotavirus Test Kits
• Rotavirus Test, Gastroenteritis
• Rubella Latex Agglutination Assay (FDA Code: LQN / 866.3510)
Rubella virus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to rubella virus in serum. The identification aids in the diagnosis of rubella (German measles) or confirmation of a person's immune status from past infections or immunizations and provides epidemiological information on German measles. Newborns infected in the uterus with rubella virus may be born with multiple congenital defects (rubella syndrome).
• Rubella Testing
• Specialty Diagnostic Supplies
• Stationary Test Tube Incubator
• Streptococcus Spp Antigen (FDA Code: GTY / 866.3740)
• Streptococcus Spp Antiserum (FDA Code: GTZ / 866.3740)
• Streptococcus Test Kits
• Swabs, Streptococcus Test Kits
• Temperature Controlled Laboratory Incubators
• Urine Screening Kit (FDA Code: JXA / 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.
• Water-microbiology kit

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