Npbi Intl. Bv

Address: Runde Zz 41, Emmer Compascuum, HM 7881, Netherlands
Phone: 49-617-26080 | Map/Directions >>

Profile: Npbi Intl. Bv deals with medical devices and diagnostics. We supply medical, precision and optical instruments.

FDA Registration Number: 9610969
US Agent: Cheryl Roscher / Fresenius Kabi Llc
Phone: +1-(847)-550-7909 E-Mail:

12 Products/Services (Click for related suppliers)

• Autotransfusion Apparatus (FDA Code: CAC / 868.5830)

An autotransfusion apparatus is a device used to collect and reinfuse the blood lost by a patient due to surgery or trauma.

• Blood & Components Collection Container (FDA Code: KSR / 864.9100)

An empty container for the collection and processing of blood and blood components is a device intended for medical purposes that is an empty plastic bag or plastic or glass bottle used to collect, store, or transfer blood and blood components for further processing.

• Blood Bank Supplies (FDA Code: KSS / 864.9050)

Blood bank supplies are general purpose devices intended for in vitro use in blood banking. This generic type of device includes products such as blood bank pipettes, blood grouping slides, blood typing tubes, blood typing racks, and cold packs for antisera reagents. The device does not include articles that are licensed by the Center for Biologics Evaluation and Research of the Food and Drug Administration.

• 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.

• Blood Transfer Unit (FDA Code: KSB / 864.9875)

A transfer set is a device intended for medical purposes that consists of a piece of tubing with suitable adaptors used to transfer blood or plasma from one container to another.

• Cardiopulmonary Bypass Blood Reservoir (FDA Code: DTN / 870.4400)

A cardiopulmonary bypass blood reservoir is a device used in conjunction with short-term extracorporeal circulation devices to hold a reserve supply of blood in the bypass circulation.

• Heat-Sealing Device (FDA Code: KSD / 864.9750)

A heat-sealing device is a device intended for medical purposes that uses heat to seal plastic bags containing blood or blood components.

• Hematocrit Tube Rack (FDA Code: GHY / 864.6400)

A hematocrit measuring device is a system consisting of instruments, tubes, racks, and a sealer and a holder. The device is used to measure the packed red cell volume in blood to determine whether the patient's total red cell volume is normal or abnormal. Abnormal states include anemia (an abnormally low total red cell volume) and erythrocytosis (an abnormally high total red cell mass). The packed red cell volume is produced by centrifuging a given volume of blood.

• High Permeability with/without Sealed Dialysate System (FDA Code: KDI / 876.5860)

A high permeability hemodialysis system is a device intended for use as an artificial kidney system for the treatment of patients with renal failure, fluid overload, or toxemic conditions by performing such therapies as hemodialysis, hemofiltration, hemoconcentration, and hemodiafiltration. Using a hemodialyzer with a semipermeable membrane that is more permeable to water than the semipermeable membrane of the conventional hemodialysis system (876.5820), the high permeability hemodialysis system removes toxins or excess fluid from the patient's blood using the principles of convection (via a high ultrafiltration rate) and/or diffusion (via a concentration gradient in dialysate). During treatment, blood is circulated from the patient through the hemodialyzer's blood compartment, while the dialysate solution flows countercurrent through the dialysate compartment. In this process, toxins and/or fluid are transferred across the membrane from the blood to the dialysate compartment. The hemodialysis delivery machine controls and monitors the parameters related to this processing, including the rate at which blood and dialysate are pumped through the system, and the rate at which fluid is removed from the patient. The high permeability hemodialysis system consists of the following devices:

• I.V. Fluid Transfer Unit (FDA Code: LHI / 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.

• Intravenous Administration Kit (FDA Code: FPA / 880.5440)

• Therapeutic Automated Blood Cell and Plasma Separator (FDA Code: LKN)