IDX Systems Corporation

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Contact: Robert Galin - SVP Sales
Web: http://www.idx.com
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idx.com
Address: 1400 Shelburne Rd., Burlington, Vermont 05402-1070, USA
Phone: +1-(802)-862-1022 | Fax: +1-(802)-862-9591 | Map/Directions >>

Profile: Providers of: Markets software and hardware products, operating systems, communication and installation services, and training to group practices, clinics, managed care organizations, faculty practice plans, imaging centers, laboratories, hospitals and multi-entity organizations. Markets software and hardware products, operating systems, communication and installation services, and training to group practices, clinics, managed care organizations, faculty practice plans, imaging centers, hospitals and integrated delivery networks. IDXTENDR is a relational, scaleable product line that leverages advanced client-server architecture and web-based technology to facilitate the flow of patient data in healthcare settings. IDXTENDR provides a relational solution designed to grow as your organization grows and comes packaged to meet your specific site requirements whether you are a group practice, MSO, hospital, or integrated delivery network (IDN). Picture archiving and communications system.

The company has ~2250 employees. NYSE:GE (SEC Filings)

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• Pediatric Apnea Monitors

• Pediatric Vital Signs Monitors

• Perinatal Monitoring System (FDA Code: HGM / 884.2740)

A perinatal monitoring system is a device used to show graphically the relationship between maternal labor and the fetal heart rate by means of combining and coordinating uterine contraction and fetal heart monitors with appropriate displays of the well-being of the fetus during pregnancy, labor, and delivery. This generic type of device may include any of the devices subject to 884.2600, 884.2640, 884.2660, 884.2675, 884.2700, and 884.2720. This generic type of device may include the following accessories: Central monitoring system and remote repeaters, signal analysis and display equipment, patient and equipment supports, and component parts.

• Personnel Protective Shield (FDA Code: KPY / 892.6500)

A personnel protective shield is a device intended for medical purposes to protect the patient, the operator, or other persons from unnecessary exposure to radiation during radiologic procedures by providing an attenuating barrier to radiation. This generic type of device may include articles of clothing, furniture, and movable or stationary structures.

• Physician, Clinical Information System

• Platinum Titanium Gold Sealed Isotope Source (FDA Code: IWI / 892.5730)

A radionuclide brachytherapy source is a device that consists of a radionuclide which may be enclosed in a sealed container made of gold, titanium, stainless steel, or platinum and intended for medical purposes to be placed onto a body surface or into a body cavity or tissue as a source of nuclear radiation for therapy.

• Pocket Halogen Otoscopes

• Portable Defibrillators

• Portable ECG Long-Term Recorder

• Portable Handheld Water Quality Multiparameter Monitor

• Portable Ultrasound Bladder Scanner

• Positron Emission Tomography

• Powered Treadmill (FDA Code: IOL / 890.5380)

Powered exercise equipment consist of powered devices intended for medical purposes, such as to redevelop muscles or restore motion to joints or for use as an adjunct treatment for obesity. Examples include a powered treadmill, a powered bicycle, and powered parallel bars.

• Pre-Operative Testing, A-Scan Ultrasound Devices

• Pre-Operative Testing, B-Scan Ultrasound Devices

• Pressure Tubing and Accessories (FDA Code: BYX / 868.5860)

Pressure tubing and accessories are flexible or rigid devices intended to deliver pressurized medical gases.

• Procedure Kits & Packs

• Programmable Diagnostic Computer (FDA Code: DQK / 870.1425)

A programmable diagnostic computer is a device that can be programmed to compute various physiologic or blood flow parameters based on the output from one or more electrodes, transducers, or measuring devices; this device includes any associated commercially supplied programs.

• Protective Restraint (FDA Code: FMQ / 880.6760)

A protective restraint is a device, including but not limited to a wristlet, anklet, vest, mitt, straight jacket, body/limb holder, or other type of strap, that is intended for medical purposes and that limits the patient's movements to the extent necessary for treatment, examination, or protection of the patient or others.

• Pulmonary Function Monitors

• Pulse Oximeters

• Pulse Rate Monitors

• R-Wave (ECG) Heart Rate Monitor

• Radiofrequency Physiological Transmitter/Receiver System (FDA Code: DRG / 870.2910)

A radiofrequency physiological signal transmitter and receiver is a device used to condition a physiological signal so that it can be transmitted via radiofrequency from one location to another, e.g., a central monitoring station. The received signal is reconditioned by the device into its original format so that it can be displayed.

• Radiographic Anthropomorphic Phantom (FDA Code: IXG / 892.1950)

A radiographic anthropomorphic phantom is a device intended for medical purposes to simulate a human body for positioning radiographic equipment.

• Radiographic Film Illuminator (FDA Code: IXC / 892.1890)

A radiographic film illuminator is a device containing a visible light source covered with a translucent front that is intended to be used to view medical radiographs.

• Radiographic Film Marking X-Ray System (FDA Code: JAC / 892.1640)

A radiographic film marking system is a device intended for medical purposes to add identification and other information onto radiographic film by means of exposure to visible light.

• Radiographic Film/Cassette Changer (FDA Code: KPX / 892.1860)

A radiographic film/cassette changer is a device intended to be used during a radiologic procedure to move a radiographic film or cassette between x-ray exposures and to position it during the exposure.

• Radiographic Test Pattern (FDA Code: IXF / 892.1940)

A radiologic quality assurance instrument is a device intended for medical purposes to measure a physical characteristic associated with another radiologic device.

• Radiography, Digital Devices

• Radiologic Contrast Media (FDA Code: KTA)

• Radiological Digital Image Communication System (FDA Code: LMD / 892.2020)

A medical image communications device provides electronic transfer of medical image data between medical devices. It may include a physical communications medium, modems, interfaces, and a communications protocol.

• Radiological Digital Image Storage Device (FDA Code: LMB / 892.2010)

A medical image storage device is a device that provides electronic storage and retrieval functions for medical images. Examples include devices employing magnetic and optical discs, magnetic tape, and digital memory.

• Radiological Image Processing System (FDA Code: LLZ / 892.2050)

A picture archiving and communications system is a device that provides one or more capabilities relating to the acceptance, transfer, display, storage, and digital processing of medical images. Its hardware components may include workstations, digitizers, communications devices, computers, video monitors, magnetic, optical disk, or other digital data storage devices, and hardcopy devices. The software components may provide functions for performing operations related to image manipulation, enhancement, compression or quantification.

• Radiology Computer Software

• Radionuclide Brachytherapy Source (FDA Code: KXK / 892.5730)

• Real-Time Ambulatory ECG Monitor

• Recording ECG Long-Term Scanner

• Refurbished Ultrasound Equipment

• Respiratory Monitors

• Ruler and Caliper (FDA Code: FTY / 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.

• Single-Function Pre-Programmed Diagnostic Computer (FDA Code: DXG / 870.1435)

A single-function, preprogrammed diagnostic computer is a hard-wired computer that calculates a specific physiological or blood-flow parameter based on information obtained from one or more electrodes, transducers, or measuring devices.

• Sleep Oximeters

• Solid State X-Ray Imager (FDA Code: MQB / 892.1680)

An image-intensified fluoroscopic x-ray system is a device intended to visualize anatomical structures by converting a pattern of x-radiation into a visible image through electronic amplification. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

• Sophisticated Ultrasound Equipment

• Specialty Magnetic Resonance Coil (FDA Code: MOS / 892.1000)

A magnetic resonance diagnostic device is intended for general diagnostic use to present images which reflect the spatial distribution and/or magnetic resonance spectra which reflect frequency and distribution of nuclei exhibiting nuclear magnetic resonance. Other physical parameters derived from the images and/or spectra may also be produced. The device includes hydrogen-1 (proton) imaging, sodium-23 imaging, hydrogen-1 spectroscopy, phosphorus-31 spectroscopy, and chemical shift imaging (preserving simultaneous frequency and spatial information).

• Specified Concentration Calibration Gas (FDA Code: BXK / 868.6400)

A calibration gas is a device consisting of a container of gas of known concentration intended to calibrate medical gas concentration measurement devices.

• Sphygmomanometer Aids

• Sphygmomanometers