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Instrumentarium Corp.


Address: PO Box 100, Kuortaneenkatu 2, Helsinki FIN-00031, Finland
Phone: +358-(10)-394-11 | Fax: +358-(9)-146-4172 | Map/Directions >>
 
 

Profile: Instrumentarium Corp. manufactures anesthesia machines, patient monitoring devices, drug delivery systems, medical & dental X-ray equipment, and infant care systems.

The company has revenues of USD 100-500 Million, has ~3600 employees and is ISO 9000, CE certified.

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• Hemodialysis Fistula Needles
• Hemodialysis Tubing Kit
• Hemodialysis Unit Blood Line Clamp
• Hemodialysis Unit Conductivity Monitor
• Hemodialysis Unit Single Needle Controller
• Hemodialysis Units
• Hemofiltration Unit
• Hemoperfusion System
• 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:
• Hollow Fiber Capillary Dialyzer (FDA Code: FJI / 876.5820)
A hemodialysis 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 an extracorporeal blood system, a conventional dialyzer, a dialysate delivery system, and accessories. Blood from a patient flows through the tubing of the extracorporeal blood system and accessories to the blood compartment of the dialyzer, then returns through further tubing of the extracorporeal blood system to the patient. The dialyzer has two compartments that are separated by a semipermeable membrane. While the blood is in the blood compartment, undesirable substances in the blood pass through the semipermeable membrane into the dialysate in the dialysate compartment. The dialysate delivery system controls and monitors the dialysate circulating through the dialysate compartment of the dialyzer.
• Holter ECG Monitors
• Holter ECG Monitors, 24 Hour Holter Monitor
• Holter ECG Monitors, Analog Holter
• Holter ECG Monitors, Cassette Tape Recorder
• Holter ECG Monitors, Digital Compact Flash Holter Recorder
• Holter ECG Monitors, Digital Holter Recorder
• Holter ECG Monitors, ECG System
• Holter ECG Monitors, Holter Heart Monitor
• Indirect Blood Pressure Monitor
• 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.
• Mammographic X-Ray System (FDA Code: IZH / 892.1710)
A mammographic x-ray system is a device intended to be used to produce radiographs of the breast. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.
• Medical Ultraviolet Water Purifiers (FDA Code: KMG / 880.6710)
A medical ultraviolet water purifier is a device intended for medical purposes that is used to destroy bacteria in water by exposure to ultraviolet radiation.
• Metabolism Analyzer
• Miniaturized Optical Pulse Oximeter Tester
• Monitoring Spirometer (FDA Code: BZK / 868.1850)
A monitoring spirometer is a device used to measure continuously a patient's tidal volume (volume of gas inhaled by the patient during each respiration cycle) or minute volume (the tidal volume multiplied by the rate of respiration for 1 minute) for the evaluation of the patient's ventilatory status.
• Nasal Suction Regulator
• Nasogastric Tube Holder
• Nasogastric Tubes (FDA Code: BSS / 876.5980)
A gastrointestinal tube and accessories is a device that consists of flexible or semi-rigid tubing used for instilling fluids into, withdrawing fluids from, splinting, or suppressing bleeding of the alimentary tract. This device may incorporate an integral inflatable balloon for retention or hemostasis. This generic type of device includes the hemostatic bag, irrigation and aspiration catheter (gastric, colonic, etc.), rectal catheter, sterile infant gavage set, gastrointestinal string and tubes to locate internal bleeding, double lumen tube for intestinal decompression or intubation, feeding tube, gastroenterostomy tube, Levine tube, nasogastric tube, single lumen tube with mercury weight balloon for intestinal intubation or decompression, and gastro-urological irrigation tray (for gastrological use).
• Non-Heated Anesthesia Vaporizer (FDA Code: CAD / 868.5880)
An anesthetic vaporizer is a device used to vaporize liquid anesthetic and deliver a controlled amount of the vapor to the patient.
• Non-Powered Traction Apparatus (FDA Code: HST / 888.5850)
A nonpowered orthopedic traction apparatus is a device that consists of a rigid frame with nonpowered traction accessories, such as cords, pulleys, or weights, and that is intended to apply a therapeutic pulling force to the skeletal system.
• Operating-Room Electrical Table (FDA Code: GDC / 878.4960)
Operating tables and accessories and operating chairs and accessories are AC-powered or air-powered devices, usually with movable components, intended for use during diagnostic examinations or surgical procedures to support and position a patient.
• Oximeters (FDA Code: DQA / 870.2700)
An oximeter is a device used to transmit radiation at a known wavelength(s) through blood and to measure the blood oxygen saturation based on the amount of reflected or scattered radiation. It may be used alone or in conjunction with a fiberoptic oximeter catheter.
• Oxygen Alarm Monitor
• Parallel Flow Dialyzer (FDA Code: FJG / 876.5820)
• Pediatric Pulse Oximeter
• Peritoneal Dialysis Tubing Kit
• Portable Pulse Oximeter
• Product Development, Micro pH Electrodes
• Product Development, Pulse Oximeter
• Protein Fractionation Densitometric Test (FDA Code: JQJ / 862.1630)
A protein (fractionation) test system is a device intended to measure protein fractions in blood, urine, cerebrospinal fluid, and other body fluids. Protein fractionations are used as an aid in recognizing abnormal proteins in body fluids and genetic variants of proteins produced in diseases with tissue destruction.
• Pulse Oximeter Accessories
• Pulse Oximeter Adapter Cables
• Pulse Oximeter Connector Cables
• Pulse Oximeter Finger Clip
• Pulse Oximeter Machines
• Pulse Oximeter Patient Cable
• Pulse Oximeter Probe Wrap
• Pulse Oximeter Sensor Repair Kits
• Pulse Oximeter Sensors Service and Repair
• Pulse Oximeter Simulator

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