Greiner Bio-One Gmbh,

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Web: http://www.greinerbioone.com/en/row/start
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Address: Bad Haller Strasse 32, Kremsmunster A-4550, Austria
Phone: +43-(7583)-6791-0 | Map/Directions >>

Profile: Greiner Bio-One Gmbh specializes in laboratory products. We offer pipettes, reaction tubes, analyzer cups, multi-purpose beakers and sealers. Our Leucosep™ offers efficient separation of lymphocytes and mononuclear cells from peripheral blood & bone marrow. Its features include enrichment directly from whole blood, rapid separation in 15 minutes at room temperature, removal of erythrocytes & granulocytes, and does not block marker molecules. Our reaction tubes have high temperature and chemical resistance.

FDA Registration Number: 8020040
US Agent: Manfred Abel / Greiner Vacuette North America, Inc.
Phone: +1-(704)-261-7800 Fax: +1-(704)-261-7899 E-Mail:

23 Products/Services (Click for related suppliers)

• Blood Collection Lancet (FDA Code: FMK / 878.4800)

A manual surgical instrument for general use is a nonpowered, hand-held, or hand-manipulated device, either reusable or disposable, intended to be used in various general surgical procedures. The device includes the applicator, clip applier, biopsy brush, manual dermabrasion brush, scrub brush, cannula, ligature carrier, chisel, clamp, contractor, curette, cutter, dissector, elevator, skin graft expander, file, forceps, gouge, instrument guide, needle guide, hammer, hemostat, amputation hook, ligature passing and knot-tying instrument, knife, blood lancet, mallet, disposable or reusable aspiration and injection needle, disposable or reusable suturing needle, osteotome, pliers, rasp, retainer, retractor, saw, scalpel blade, scalpel handle, one-piece scalpel, snare, spatula, stapler, disposable or reusable stripper, stylet, suturing apparatus for the stomach and intestine, measuring tape, and calipers. A surgical instrument that has specialized uses in a specific medical specialty is classified in separate regulations in parts 868 through 892.

• 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 Mixing and Weighing Device (FDA Code: KSQ / 864.9195)

A blood mixing device is a device intended for medical purposes that is used to mix blood or blood components by agitation. A blood weighing device is a device intended for medical purposes that is used to weigh blood or blood components as they are collected.

• Erythrocyte Sedimentation Rate Test (FDA Code: JPH / 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.

• General Purpose Reagent (FDA Code: LDT)

• Injection Cannula (FDA Code: FGY / 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.

• Intravenous Administration Kit (FDA Code: FPA / 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.

• Micro Pipette (FDA Code: JRC / 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.

• Microbiology Diagnostic Device (FDA Code: LIB / 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.

• Mycoplasma Detection Kit (FDA Code: KIW / 864.2360)

Mycoplasma detection media and components are used to detect and isolate mycoplasma pleuropneumonia-like organisms (PPLO), a common microbial contaminant in cell cultures.

• 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-Sterile Specimen Container (FDA Code: NNI / 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.

• Non-Sterile Specimen Mailer And Storage Container (FDA Code: NNK / 864.3250)

• Pasteur Pipettes (FDA Code: GJW / 864.6160)

A manual blood cell counting device is a device used to count red blood cells, white blood cells, or blood platelets.

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

• 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.

• 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 Container (FDA Code: FMH / 864.3250)

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

• Thermostated Cuvette (FDA Code: JRI / 862.2050)

• 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 Tube (FDA Code: KJG / 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.

• Vacuum Sample Tube with Anticoagulant (FDA Code: GIM / 862.1675)