Profile: Philips Medical Systems, N.A. manufactures systems for imaging, radiation oncology & patient monitoring, as well as renders information management & resuscitation products. Our heartstart home defibrillator helps in situations where a sudden cardiac arrest strikes. Our ambient light technology is a theater lighting system that actively adjusts both brightness & color based upon picture content. Our Respironics V200 Critical Care Ventilator provides state-of-the-art ventilation modes with synchrony options that reduce work of breathing and streamline patient care.

The company has revenues of > USD 1 Billion, has ~35550 employees. NYSE:PHG (SEC Filings)

FDA Registration Number: 1218950

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• Emission Computed Tomography System (FDA Code: KPS / 892.1200) An emission computed tomography system is a device intended to detect the location and distribution of gamma ray- and positron-emitting radionuclides in the body and produce cross-sectional images through computer reconstruction of the data. This generic type of device may include signal analysis and display equipment, patient and equipment supports, radionuclide anatomical markers, component parts, and accessories.

• Esophageal Stethoscopes (FDA Code: BZW / 868.1910) An esophageal stethoscope is a nonpowered device that is inserted into a patient's esophagus to enable the user to listen to heart and breath sounds.

• Esophageal Stethoscopes with Temperature

• Event ECG Monitors

• Extension Airway Connector (FDA Code: BZA / 868.5810) An airway connector is a device intended to connect a breathing gas source to a tracheal tube, tracheostomy tube, or mask.

• Extra-Long Length Esophageal Stethoscope

• Extracorporeal Lithotripsy (ESWL) Systems

• Fetal Doppler Ultrasound Monitor (FDA Code: MAA / 884.2660) A fetal ultrasonic monitor is a device designed to transmit and receive ultrasonic energy into and from the pregnant woman, usually by means of continuous wave (doppler) echoscopy. The device is used to represent some physiological condition or characteristic in a measured value over a period of time (e.g., perinatal monitoring during labor) or in an immediately perceptible form (e.g., use of the ultrasonic stethoscope). This generic type of device may include the following accessories: signal analysis and display equipment, electronic interfaces for other equipment, patient and equipment supports, and component parts. This generic type of device does not include devices used to image some relatively unchanging physiological structure or interpret a physiological condition, but does include devices which may be set to alarm automatically at a predetermined threshold value.

• Fetal pulse Oximetry

• Full Body X-Ray Computed Tomography Scanner

• Gaseous Phase Carbon-Dioxide Gas Analyzer (FDA Code: CCK / 868.1400) A carbon dioxide gas analyzer is a device intended to measure the concentration of carbon dioxide in a gas mixture to aid in determining the patient's ventilatory, circulatory, and metabolic status. The device may use techniques such as chemical titration, absorption of infrared radiation, gas chromatography, or mass spectrometry.

• Gaseous Phase Oxygen Gas Analyzer (FDA Code: CCL / 868.1720) An oxygen gas analyzer is a device intended to measure the concentration of oxygen in respiratory gases by techniques such as mass spectrometry, polarography, thermal conductivity, or gas chromatography. This generic type of device also includes paramagnetic analyzers.

• General Purpose Ultrasonic Scanner

• Handheld Pulse Oximeter

• Heart CT Scan

• Helical CT Scan

• High Voltage Therapeutic X-Ray Collimator (FDA Code: IYK / 892.5900) An x-ray radiation therapy system is a device intended to produce and control x-rays used for radiation therapy. This generic type of device may include signal analysis and display equipment, patient and equipment supports, treatment planning computer programs, component parts, and accessories.

• High Voltage Therapeutic X-Ray Generator

• Holter Management Software

• Image-Intensified Fluoroscopic X-Ray System (FDA Code: JAA / 892.1650) 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.

• Indirect Blood Pressure Monitor

• Industrial X-Ray Tube

• Infrared Physiological Signal Transmitter/Receiver

• Internal Defibrillators

• Light Beam Patient Position Monitor (FDA Code: IWE / 892.5780) A light beam patient position indicator is a device that projects a beam of light (incoherent light or laser) to determine the alignment of the patient with a radiation beam. The beam of light is intended to be used during radiologic procedures to ensure proper positioning of the patient and to monitor alignment of the radiation beam with the patient's anatomy.

• Limboardr Arm Boards

• Low Voltage Therapeutic X-Ray Collimator (FDA Code: IYJ / 892.5900)

• Low Voltage Therapeutic X-Ray Generator (FDA Code: IYD / 892.5900)

• Manual Radiographic Collimator (FDA Code: IZX / 892.1610) A diagnostic x-ray beam-limiting device is a device such as a collimator, a cone, or an aperture intended to restrict the dimensions of a diagnostic x-ray field by limiting the size of the primary x-ray beam.

• Medical Cathode-Ray Tube Display (FDA Code: DXJ / 870.2450) A medical cathode-ray tube display is a device designed primarily to display selected biological signals. This device often incorporates special display features unique to a specific biological signal.

• Medical CT Scan

• Medical Magnetic Tape Recorder (FDA Code: DSH / 870.2800) A medical magnetic tape recorder is a device used to record and play back signals from, for example, physiological amplifiers, signal conditioners, or computers.

• Mobile C-Arm Radiographic/Fluoroscopic Unit

• Mobile Fluoroscopic X-Ray System (FDA Code: IZL / 892.1720) A mobile x-ray system is a transportable device system intended to be used to generate and control x-ray for diagnostic procedures. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

• Mobile Obstetrical/Gynecological Ultrasonic Scanner

• Mobile X-Ray System (FDA Code: IZL / 892.1720)

• Motorized Mobile X-Ray System

• MRI Imaging

• Non-Continuous Ventilator/Respirator (FDA Code: BZD / 868.5905) A noncontinuous ventilator (intermittent positive pressure breathing-IPPB) is a device intended to deliver intermittently an aerosol to a patient's lungs or to assist a patient's breathing.

• Nuclear Magnetic Resonance Imaging System (FDA Code: LNH / 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).

• Obstetric Ultrasonic Transducer (FDA Code: HGL / 884.2960) An obstetric ultrasonic transducer is a device used to apply ultrasonic energy to, and to receive ultrasonic energy from, the body in conjunction with an obstetric monitor or imager. The device converts electrical signals into ultrasonic energy, and vice versa, by means of an assembly distinct from an ultrasonic generator. This generic type of device may include the following accessories: coupling gel, preamplifiers, amplifiers, signal conditioners with their power supply, connecting cables, and component parts. This generic type of device does not include devices used to generate the ultrasonic frequency electrical signals for application.

• Orthovoltage Therapeutic X-Ray Collimator (FDA Code: IYI / 892.5900)

• 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.

• Patient Cart

• Patient Physiological Monitor (FDA Code: MHX / 870.1025) The arrhythmia detector and alarm device monitors an electrocardiogram and is designed to produce a visible or audible signal or alarm when atrial or ventricular arrhythmia, such as premature contraction or ventricular fibrillation, occurs.

• Patient Physiological Monitor without Arrhythmia Detection (FDA Code: MWI / 870.2300) A cardiac monitor (including cardiotachometer and rate alarm) is a device used to measure the heart rate from an analog signal produced by an electrocardiograph, vectorcardiograph, or blood pressure monitor. This device may sound an alarm when the heart rate falls outside preset upper and lower limits.

• Patient Position Support (FDA Code: CCX / 868.6820) A patient position support is a device intended to maintain the position of an anesthetized patient during surgery.

• Patient Stand-On Scale (FDA Code: FRI / 880.2700) A stand-on patient scale is a device intended for medical purposes that is used to weigh a patient who is able to stand on the scale platform.

• Pediatric Ultrasonic Scanner

• Phonocardiograph (FDA Code: DQC / 870.2390) A phonocardiograph is a device used to amplify or condition the signal from a heart sound transducer. This device furnishes the excitation energy for the transducer and provides a visual or audible display of the heart sounds.