Profile: Whatman specializes in separations technology. We are an ISO 9001, ISO 9002, CE MARK certified company. We provide products and solutions. Our product ranges from filter papers & membranes to disposable filtration devices, groundbreaking technology for capturing, archiving and purifying DNA at room temperature. Our Steri CleanZ™ filter devices for hospital wash water & equipment sterilization have been tested & proven to render sterile point of use solutions. Our microplate technology is applied by a team of engineers, scientists, polymer engineers, and filtration experts to ensure Whatman with the leading edge of new developments. Our multiwell range of products is extremely diverse. The novel design of the filter plates allows for a large number of applications. Applications for disciplines such as sample preparation, genomics, and filter based assays are served by the multiwell approach to filtration technology.
The company was founded in 1760, has revenues of USD 50-100 Million, has ~850 employees and is ISO 9001, ISO 9002, CE certified.
38 Products/Services (Click for related suppliers)
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• Adhesive operation Paper |
• Air Filters |
• Arterial Line Cardiopulmonary Bypass Blood Filter (FDA Code: DTM / 870.4260) A cardiopulmonary bypass arterial line blood filter is a device used as part of a gas exchange (oxygenator) system to filter nonbiologic particles and emboli (blood clots or pieces of foreign material flowing in the bloodstream which will obstruct circulation by blocking a vessel) out of the blood. It is used in the arterial return line. |
• Arthroscopic Insufflator |
• Aspirator Filter |
• Blood Collection Systems (FDA Code: JKA / 862.1675) A blood specimen collection device is a device intended for medical purposes to collect and to handle blood specimens and to separate serum from nonserum (cellular) components prior to further testing. This generic type device may include blood collection tubes, vials, systems, serum separators, blood collection trays, or vacuum sample tubes. |
• Blood Transfusion Microfilter (FDA Code: CAK / 880.5440) An intravascular administration set is a device used to administer fluids from a container to a patient's vascular system through a needle or catheter inserted into a vein. The device may include the needle or catheter, tubing, a flow regulator, a drip chamber, an infusion line filter, an I.V. set stopcock, fluid delivery tubing, connectors between parts of the set, a side tube with a cap to serve as an injection site, and a hollow spike to penetrate and connect the tubing to an I.V. bag or other infusion fluid container. |
• Blot Transfer Kits (Capillary) |
• Breathing Circuit Bacterial Filter (FDA Code: CAH / 868.5260) A breathing circuit bacterial filter is a device that is intended to remove microbiological and particulate matter from the gases in the breathing circuit. |
• Cardiopulmonary Pre-Bypass Filter (FDA Code: KRJ / 870.4280) A cardiopulmonary prebypass filter is a device used during priming of the oxygenator circuit to remove particulates or other debris from the circuit prior to initiating bypass. The device is not used to filter blood. |
• Charcoal Water Purification Filter |
• Chromatography Column |
• Dot & Slot Blotters |
• Durable Product Contract Manufacturing |
• Electrodes and Other Components, Gold Cup Electrodes |
• Filter Paper |
• Gas Filter |
• Gas Filtering Tubes |
• Hydrophilic Membrane Filter |
• Hydrophobic Membrane Filter |
• Infusion Line Filter (FDA Code: FPB / 880.5440) |
• Intravenous Tubing Filter |
• Ion Paper (FDA Code: DMG / 862.2230) A chromatographic separation material for clinical use is a device accessory (e.g., ion exchange absorbents, ion exchagne resins, and ion papers) intended for use in ion exchange chromatography, a procedure in which a compound is separated from a solution. |
• Labeled Medical Laboratory Equipment (FDA Code: LXG / 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. |
• Laboratory Bacteriological Filter |
• Liquid Chromatography Equipment |
• Membrane Filter Holder |
• Microporous Membrane Filter |
• Paper Chromatography Equipment |
• Particulate Membrane Filter |
• Particulate Water Purification Filter |
• Peritoneal Dialysate Filter (FDA Code: KPP / 876.5630) (1) A peritoneal dialysis system and accessories is a device that is used as an artificial kidney system for the treatment of patients with renal failure or toxemic conditions, and that consists of a peritoneal access device, an administration set for peritoneal dialysis, a source of dialysate, and, in some cases, a water purification mechanism. After the dialysate is instilled into the patient's peritoneal cavity, it is allowed to dwell there so that undesirable substances from the patient's blood pass through the lining membrane of the peritoneal cavity into this dialysate. These substances are then removed when the dialysate is drained from the patient. The peritoneal dialysis system may regulate and monitor the dialysate temperature, volume, and delivery rate together with the time course of each cycle of filling, dwell time, and draining of the peritoneal cavity or manual controls may be used. This generic device includes the semiautomatic and the automatic peritoneal delivery system. |
• Steam Filter |
• Syringe Filter |
• Thin Layer Chromatography Equipment (FDA Code: DPA / 862.2270) A thin-layer chromatography (TLC) system for clinical use is a device intended to separate one or more drugs or compounds from a mixture. The mixture of compounds is absorbed onto a stationary phase or thin layer of inert material (e.g., cellulose, alumina, etc.) and eluted off by a moving solvent (moving phase) until equilibrium occurs between the two phases. |
• Thin Layer Chromatography Sprayer |
• Ventilator Filter with Flexible Coupler |
• Ventilator Filters |