SeraCare Life Sciences, Inc.

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Web: http://www.seracare.com
E-Mail:
Address: 37 Birch Street, Milford, Massachusetts 01757, USA
Phone: +1-(508)-244-6400 | Fax: +1-(508)-580-2202 | Map/Directions >>
 
 

Profile: SeraCare Life Sciences, Inc. manufactures and sells biological based materials. We focus on biotechnology, pharmaceutical and diagnostic industries. We are certified with ISO 13485 standard. Our products are used by test kit manufacturers, infectious disease researchers and regulatory agencies. We also supply to independent clinical laboratories, hospitals, public health laboratories, blood banks and plasma collection centers.

The company was founded in 1984, has revenues of USD 25-50 Million, has ~50 employees and is ISO certified. OTC:SRLS (SEC Filings)

FDA Registration Number: 3007088335

35 Products/Services (Click for related suppliers)  
• Assayed and Unassayed Single (Specified) Analyte Controls (FDA Code: JJX / 862.1660)
A quality control material (assayed and unassayed) for clinical chemistry is a device intended for medical purposes for use in a test system to estimate test precision and to detect systematic analytical deviations that may arise from reagent or analytical instrument variation. A quality control material (assayed and unassayed) may be used for proficiency testing in interlaboratory surveys. This generic type of device includes controls (assayed and unassayed) for blood gases, electrolytes, enzymes, multianalytes (all kinds), single (specified) analytes, or urinalysis controls.
• Automated Pipetter
• Benchtop Centrifuges
• Blood Bank Test Kits
• Blood Culture Instruments
• Blood Culture Test Kits
• Centrifuges
• Clinical Laboratory Information Systems (LIS)
• Cotton Swabs
• Cytomegalovirus Virus IF Antibody Igm Test (FDA Code: LKQ / 866.3175)
Cytomegalovirus serological reagents are devices that consist of antigens and antisera used in serological tests to identify antibodies to cytomegalovirus in serum. The identification aids in the diagnosis of diseases caused by cytomegaloviruses (principally cytomegalic inclusion disease) and provides epidemiological information on these diseases. Cytomegalic inclusion disease is a generalized infection of infants and is caused by intrauterine or early postnatal infection with the virus. The disease may cause severe congenital abnormalities, such as microcephaly (abnormal smallness of the head), motor disability, and mental retardation. Cytomegalovirus infection has also been associated with acquired hemolytic anemia, acute and chronic hepatitis, and an infectious mononucleosis-like syndrome.
• DNA Amplification For GC/CT Instruments
• Fertility Products, Human Serum Albumin
• Gliadin Antibodies (FDA Code: MST / 866.5750)
A radioallergosorbent immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the allergen antibodies (antibodies which cause an allergic reaction) specific for a given allergen. Measurement of specific allergen antibodies may aid in the diagnosis of asthma, allergies, and other pulmonary disorders.
• Hematology Controls Cbc
• Human and Animal Sera (FDA Code: KIS / 864.2800)
Animal and human sera are biological products, obtained from the blood of humans or other animals, that provide the necessary growth-promoting nutrients in a cell culture system.
• Human Serum
• Infectious Disease Identification Test Kits
• Infectious Disease Test Kits
• Laboratory Centrifuges, Floor
• Laboratory Information Systems
• Laboratory Information Systems (LIS), Software
• Microbiology Identification Instruments
• Microbiology Identification Test Kits
• Microbiology PCR Instruments
• Microbiology Susceptibility Instruments
• Multi Analyte Control (FDA Code: JJY / 862.1660)
• Petri Plates
• Positive Control Serological Kit (FDA Code: MJX / 862.1660)
• Preps & Swabs
• Quality Control Kit for Blood Banking Reagents (FDA Code: KSF / 864.9650)
A quality control kit for blood banking reagents is a device that consists of sera, cells, buffers, and antibodies used to determine the specificity, potency, and reactivity of the cells and reagents used for blood banking.
• Susceptibility Test Kits
• Swabs
• Swabs, Absorbing
• Test(Donors) Kit For Bloodborne Pathogen (FDA Code: MYZ)
• Toxoplasma Gondii IF Antisera Test (FDA Code: LJK / 866.3780)

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