Sarstedt AG & Co.

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Web: http://www.sarstedt.com
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sarstedt.com
Address: Rommelsdorfer Straße, Postfach 1220, Numbrecht 51582, Germany
Phone: +49-(2293)-305-0 | Fax: +49-(2293)-305-282 | Map/Directions >>

Profile: Sarstedt AG & Co. manufactures & distributes equipment and consumables in the field of medicine & research. The S-Monovette® for PFA 100 contains a buffered citrate preparation that is required for use on the Dade PFA 100, particularly for patients under ASS therapy. This S-Monovette® must not be centrifuged and features a light blue screw cap to distinguish it from citrate tubes used for coagulation analysis. The S-Monovette® HCY-C is specially designed for homocysteine determination and ensures sample stability for 6 hours. The S-Monovette® is a closed blood collection system that allows the user to collect blood according to the individual patient or the condition of the veins using either the aspiration or the vacuum principle. The gentle aspiration technique has clear advantages, especially in view of the difficult vein conditions often encountered in paediatrics, geriatrics or oncology.

The company was founded in 1961, has revenues of USD 25-50 Million, has ~200 employees and is ISO 9001, CE certified.

FDA Registration Number: 2242368

51 to 96 of 96 Products/Services (Click for related suppliers) Page:

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• Medical Carts

• Medical Co2 Incubators

• Medication Carts

• Membrane Filter Unit (FDA Code: JRL / 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.

• Micro Pipette (FDA Code: JRC / 862.2050)

• Micro Pipette Tips and Tip Racks

• Microplate Incubators and Shakers

• 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.

• Neurology Instruments

• Non-Pneumatic Tourniquet (FDA Code: GAX / 878.5900)

A nonpneumatic tourniquet is a device consisting of a strap or tubing intended to be wrapped around a patient's limb and tightened to reduce circulation.

• Non-Powered Portable Single Patient Suction Apparatus (FDA Code: GCY / 878.4680)

A nonpowered, single patient, portable suction apparatus is a device that consists of a manually operated plastic, disposable evacuation system intended to provide a vacuum for suction drainage of surgical wounds.

• Non-Propagating Transport Culture Media (FDA Code: JSM / 866.2390)

A transport culture medium is a device that consists of a semisolid, usually non-nutrient, medium that maintains the viability of suspected pathogens contained in patient specimens while in transit from the specimen collection area to the laboratory. The device aids in the diagnosis of disease caused by pathogenic microorganisms and also provides epidemiological information on these diseases.

• Occult Blood Reagent (FDA Code: KHE / 864.6550)

An occult blood test is a device used to detect occult blood in urine or feces. (Occult blood is blood present in such small quantities that it can be detected only by chemical tests of suspected material, or by microscopic or spectroscopic examination.)

• Pediatric Urine Collector (FDA Code: KNX / 876.5250)

A urine collector and accessories is a device intended to collect urine. The device and accessories consist of tubing, a suitable receptacle, connectors, mechanical supports, and may include a means to prevent the backflow of urine or ascent of infection. The two kinds of urine collectors are:

• Peritoneal Catheter (FDA Code: GBW / 878.4200)

An introduction/drainage catheter is a device that is a flexible single or multilumen tube intended to be used to introduce nondrug fluids into body cavities other than blood vessels, drain fluids from body cavities, or evaluate certain physiologic conditions. Examples include irrigation and drainage catheters, pediatric catheters, peritoneal catheters (including dialysis), and other general surgical catheters. An introduction/drainage catheter accessory is intended to aid in the manipulation of or insertion of the device into the body. Examples of accessories include adaptors, connectors, and catheter needles.

• Petri Plates

• Phlebotomy Disposals

• Phlebotomy Needles & Tourniquets

• Pipettes & Tips

• Plastic Blood Lancets

• Platelet Agitators, Platelet Incubators

• Platelet Storage Environmental Chamber (FDA Code: KSH / 864.9575)

An environmental chamber for storage of platelet concentrate is a device used to hold platelet-rich plasma within a preselected temperature range.

• Pressure Infusor for I.V. Bags (FDA Code: KZD / 880.5420)

A pressure infusor for an I.V. bag is a device consisting of an inflatable cuff which is placed around an I.V. bag. When the device is inflated, it increases the pressure on the I.V. bag to assist the infusion of the fluid.

• Pyrex Test Tubes

• Red Stopper Blood Collection Tube

• Refrigerated Centrifuges (FDA Code: JQC / 862.2050)

• Reticulocyte Stain (FDA Code: GJH / 864.1850)

Dye and chemical solution stains for medical purposes are mixtures of synthetic or natural dyes or nondye chemicals in solutions used in staining cells and tissues for diagnostic histopathology, cytopathology, or hematology.

• Rimmed Glass Test Tubes

• Sedimentation Rate Tube (FDA Code: GHC / 864.6700)

An erythrocyte sedimentation rate test is a device that measures the length of time required for the red cells in a blood sample to fall a specified distance or a device that measures the degree of sedimentation taking place in a given length of time. An increased rate indicates tissue damage or inflammation.

• Single Lumen Hypodermic Needle (FDA Code: FMI / 880.5570)

A hypodermic single lumen needle is a device intended to inject fluids into, or withdraw fluids from, parts of the body below the surface of the skin. The device consists of a metal tube that is sharpened at one end and at the other end joined to a female connector (hub) designed to mate with a male connector (nozzle) of a piston syringe or an intravascular administration set.

• Specialty Diagnostic Supplies

• Specimen Collection Kits

• Stainless Steel Blood Lancets

• Sterile Absorbent Tipped Applicator (FDA Code: KXG / 880.6025)

An absorbent tipped applicator is a device intended for medical purposes that consists of an absorbent swab on a wooden, paper, or plastic stick. The device is used to apply medications to, or to take specimens from, a patient.

• Sterile Specimen Mailer and Storage Container (FDA Code: KDT / 864.3250)

A specimen transport and storage container, which may be empty or prefilled, is a device intended to contain biological specimens, body waste, or body exudate during storage and transport in order that the matter contained therein can be destroyed or used effectively for diagnostic examination. If prefilled, the device contains a fixative solution or other general purpose reagent to preserve the condition of a biological specimen added to the container. This section does not apply to specimen transport and storage containers that are intended for use as part of an over-the-counter test sample collection system for drugs of abuse testing.

• Sterile Temperature Control Specimen Mailer and Storage Container (FDA Code: KDW / 864.3250)

• Temperature Controlled Laboratory Incubators

• Test Tubes

• Tissue Culture Dish (FDA Code: KIZ / 864.2240)

Cell and tissue culture supplies and equipment are devices that are used to examine, propagate, nourish, or grow cells and tissue cultures. These include such articles as slide culture chambers, perfusion and roller apparatus, cell culture suspension systems, and tissue culture flasks, disks, tubes, and roller bottles.

• Tissue Culture Flask (FDA Code: KJA / 864.2240)

• Tissue Culture Roller Bottle (FDA Code: KJC / 864.2240)

• Tourniquets

• Umbilical Occlusion Device (FDA Code: FOD / 880.5950)

An umbilical occlusion device is a clip, tie, tape, or other article used to close the blood vessels in the umbilical cord of a newborn infant.

• Urine Collector and Accessories (FDA Code: KNX / 876.5250)

• Venous Blood Collection Tubes

• Yellow Stopper Blood Collection Tube