Profile: Thermo Fisher Scientific Inc. specializes in analytical instruments. Our unisystem pipettes are made of disposable plastic. Our finnigan LTQ linear ion trap mass spectrometer offers unparalleled sensitivity & ultra-fast cycle time to deliver more information with less sample, in less time. Our microplate instruments are ideal for cell biology, molecular biology and immunology applications in the field of cancer research, drug development, proteomics and genomics. We also offer life science research and drug discovery products for pierce protein research, HyClone cell culture, BioImage & Cellomics high content screening, Dharmacon RNA interference, Open Biosystems RNAi, gene expression & antibodies, ABgene PCR reagents & plastics, and Milwaukee nucleic acid synthesis & labeling.

The company was founded in 1956, has revenues of USD 100-500 Million, has ~870 employees and is ISO 9001, CE certified. NYSE:TMO (SEC Filings)

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• Reaction Apparatus

• Reagents

• Red Cell Storage

• Red Cell Storage and Lysis

• Refrigerated Benchtop Centrifuges

• Refrigerated Centrifuges

• Refrigerated Centrifuges (FDA Code: JQC / 862.2050) General purpose laboratory equipment labeled or promoted for a specific medical use is a device that is intended to prepare or examine specimens from the human body and that is labeled or promoted for a specific medical use.

• Refrigerated Floor Centrifuges

• Refrigerated Incubator Shaker

• Refrigerated Microcentrifuges

• Refrigerator Alarm

• Respiratory Syncytial Virus (RSV) Test Kits

• Reverse Osmosis Water Purifier Purification

• Rexam Dispensing Systems

• Rheumatoid Factor Test System (FDA Code: DHR / 866.5775) A rheumatoid factor immunological test system is a device that consists of the reagents used to measure by immunochemical techniques the rheumatoid factor (antibodies to immunoglobulins) in serum, other body fluids, and tissues. Measurement of rheumatoid factor may aid in the diagnosis of rheumatoid arthritis.

• Rotary Microtomes (FDA Code: IDO / 864.3010) Tissue processing equipment consists of devices used to prepare human tissue specimens for diagnostic histological examination by processing specimens through the various stages of decalcifying, infiltrating, sectioning, and mounting on microscope slides.

• Rotary Screw Vacuum Systems

• Rotavirus Test Kits

• Scientific Microcentrifuges

• Scientific Microhematocrit Centrifuges

• Secondary Calibrator (FDA Code: JIT / 862.1150) A calibrator is a device intended for medical purposes for use in a test system to establish points of reference that are used in the determination of values in the measurement of substances in human specimens. (See also 862.2 in this part.)

• Semi-enclosed Tissue Processors

• Sensitive Pregnancy Tests

• Serological Pipette Racks

• Serum Chemistry Controls

• Shaker/Stirrer (FDA Code: JRQ / 862.2050)

• Shaking Water Baths

• Silicone Tubing

• Silicone Tubing, Medical Grade

• Slide Stainers

• Smoke and Fume Handling Units

• SOC Media

• Sodium Flame Photometer (FDA Code: JGT / 862.1665) A sodium test system is a device intended to measure sodium in serum, plasma, and urine. Measurements obtained by this device are used in the diagnosis and treatment of aldosteronism (excessive secretion of the hormone aldosterone), diabetes insipidus (chronic excretion of large amounts of dilute urine, accompanied by extreme thirst), adrenal hypertension, Addison's disease (caused by destruction of the adrenal glands), dehydration, inappropriate antidiuretic hormone secretion, or other diseases involving electrolyte imbalance.

• Sodium Ion Specific Electrode (FDA Code: JGS / 862.1665)

• Specific Ion Electrode

• Specified Concentration Calibration Gas (FDA Code: BXK / 868.6400) A calibration gas is a device consisting of a container of gas of known concentration intended to calibrate medical gas concentration measurement devices.

• Specimen Storage Cabinets

• Stackable Incubator Shakers

• Standard Hybridization Ovens

• Staphylococcus Aureus Screening Kit (FDA Code: JWX / 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.

• Sterile Non-Barrier Pipette Tips

• Stirrer

• Stomach pH Electrode (FDA Code: FFT / 876.1400) A stomach pH electrode is a device used to measure intragastric and intraesophageal pH (hydrogen ion concentration). The pH electrode is at the end of a flexible lead which may be inserted into the esophagus or stomach through the patient's mouth. The device may include an integral gastrointestinal tube.

• Streptococcus Test Kits

• Surgical Chisels

• Swabs, Gonorrhea Test Kits

• Swabs, Influenza A, B Test Kits

• Swabs, Respiratory Syncytial Virus (RSV) Test Kits

• Swabs, Streptococcus Test Kits

• Synthetic Cell and Tissue Culture Media and Components (FDA Code: KIT / 864.2220) Synthetic cell and tissue culture media and components are substances that are composed entirely of defined components (e.g., amino acids, vitamins, inorganic salts) that are essential for the survival and development of cell lines of humans and other animals. This does not include tissue culture media for human ex vivo tissue and cell culture processing applications as described in 876.5885 of this chapter.