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

101 to 150 of 176 Products/Services (Click for related suppliers)  Page: 1 2 [3] 4

• Portable Defibrillators

• Portable Pulse Oximeter

• Portable Ultrasound Bladder Scanner

• Positive End Expiratory Pressure Breathing Attachment (FDA Code: BYE / 868.5965) A positive end expiratory pressure (PEEP) breathing attachment is a device attached to a ventilator that is used to elevate pressure in a patient's lungs above atmospheric pressure at the end of exhalation.

• Powered Non-Tilting Radiographic Table (FDA Code: IZZ / 892.1980) A radiologic table is a device intended for medical purposes to support a patient during radiologic procedures. The table may be fixed or tilting and may be electrically powered.

• Powered Radiation Therapy Couch (FDA Code: JAI / 892.5770) A powered radiation therapy patient support assembly is an electrically powered adjustable couch intended to support a patient during radiation therapy.

• 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.

• Pulse Oximeters

• Pulse Oximetry

• Pulse Oximetry Belts

• Pulse Oximetry Device

• Radiation Therapy Beam Shaping Block (FDA Code: IXI / 892.5710) A radiation therapy beam-shaping block is a device made of a highly attenuating material (such as lead) intended for medical purposes to modify the shape of a beam from a radiation therapy source.

• Radiation Therapy Treatment Planning System (FDA Code: MUJ / 892.5050) A medical charged-particle radiation therapy system is a device that produces by acceleration high energy charged particles (e.g., electrons and protons) intended for use in 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.

• Radiographic Aperture (FDA Code: IZS / 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.

• Radiographic Cone (FDA Code: IZT / 892.1610)

• Radiographic Film Changer

• Radiographic Focal Spot Camera (FDA Code: IXH / 892.1940) A radiologic quality assurance instrument is a device intended for medical purposes to measure a physical characteristic associated with another radiologic device.

• Radiographic Grid (FDA Code: IXJ / 892.1910) A radiographic grid is a device that consists of alternating radiolucent and radiopaque strips intended to be placed between the patient and the image receptor to reduce the amount of scattered radiation reaching the image receptor.

• Radiographic Head Holder (FDA Code: IWY / 892.1920) A radiographic head holder is a device intended to position the patient's head during a radiographic procedure.

• Radiographic Picture Archiving/Communication System

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

• Radiographic Urological Table

• Radiographic X-Ray Tube

• 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 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.

• Radionuclide Radiation Therapy System (FDA Code: IWB / 892.5750) A radionuclide radiation therapy system is a device intended to permit an operator to administer gamma radiation therapy, with the radiation source located at a distance from the patient's body. This generic type of device may include signal analysis and display equipment, patient and equipment supports, treatment planning computer programs, component parts (including beam-limiting devices), and accessories.

• Radionuclide Teletherapy Beam Limiting Device (FDA Code: IWD / 892.5750)

• Radionuclide Teletherapy Source (FDA Code: IWH / 892.5740) A radionuclide teletherapy source is a device consisting of a radionuclide enclosed in a sealed container. The device is intended for radiation therapy, with the radiation source located at a distance from the patient's body.

• Regular Tube Esophageal Stethoscope

• Routine EEG Systems

• Scintillation Gamma Camera (FDA Code: IYX / 892.1100) A scintillation (gamma) camera is a device intended to image the distribution of radionuclides in the body by means of a photon radiation detector. This generic type of device may include signal analysis and display equipment, patient and equipment supports, radionuclide anatomical markers, component parts, and accessories.

• Small Parts Ultrasonic Scanner

• Soft Tube Esophageal Stethoscope

• 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.

• Spot Film Device (FDA Code: IXL / 892.1670) A spot-film device is an electromechanical component of a fluoroscopic x-ray system that is intended to be used for medical purposes to position a radiographic film cassette to obtain radiographs during fluoroscopy.

• Stationary Top Radiographic Table (FDA Code: IXQ / 892.1980)

• Sterile Arm Board with Cover (FDA Code: BTX / 878.3910) A noninflatable extremity splint is a device intended to immobilize a limb or an extremity. It is not inflatable.

• Stimulator & Ultrasound Kits

• Tabletop Digital Pulse Oximeter

• Telephone Multi-Channel ECG Transmitter/Receiver System

• Telephone Single-Channel ECG Transmitter/Receiver System

• Therapeutic X-Ray Tube Housing Assembly (FDA Code: ITZ / 892.5930) A therapeutic x-ray tube housing assembly is an x-ray generating tube encased in a radiation-shielded housing intended for use in radiation therapy. This generic type of device may include high-voltage and filament transformers or other appropriate components when contained in radiation-shielded housing.

• Tilting Radiographic Table (FDA Code: IXR / 892.1980)

• Tomographic X-Ray System (FDA Code: IZF / 892.1740) A tomographic x-ray system is an x-ray device intended to be used to produce radiologic images of a specific cross-sectional plane of the body by blurring or eliminating detail from other planes. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

• Ultrasonic Device Guide

• Ultrasonic Obstetric-Gynecologic Imager (FDA Code: HEM / 884.2225) An obstetric-gynecologic ultrasonic imager is a device designed to transmit and receive ultrasonic energy into and from a female patient by pulsed echoscopy. This device is used to provide a visual representation of some physiological or artificial structure, or of a fetus, for diagnostic purposes during a limited period of time. This generic type of device may include the following: signal analysis and display equipment, electronic interfaces for other equipment, patient and equipment supports, coupling gel, and component parts. This generic type of device does not include devices used to monitor the changes in some physiological condition over long periods of time.

• Ultrasonic Puls-Echo Scanner (FDA Code: IYO / 892.1560) An ultrasonic pulsed echo imaging system is a device intended to project a pulsed sound beam into body tissue to determine the depth or location of the tissue interfaces and to measure the duration of an acoustic pulse from the transmitter to the tissue interface and back to the receiver. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

• Ultrasonic Pulsed Doppler Imaging System (FDA Code: IYN / 892.1550) An ultrasonic pulsed doppler imaging system is a device that combines the features of continuous wave doppler-effect technology with pulsed-echo effect technology and is intended to determine stationary body tissue characteristics, such as depth or location of tissue interfaces or dynamic tissue characteristics such as velocity of blood or tissue motion. This generic type of device may include signal analysis and display equipment, patient and equipment supports, component parts, and accessories.

• Ultrasonic Scanner

• Ultrasonic Transducer (FDA Code: JOP / 870.2880) An ultrasonic transducer is a device applied to the skin to transmit and receive ultrasonic energy that is used in conjunction with an echocardiograph to provide imaging of cardiovascular structures. This device includes phased arrays and two-dimensional scanning transducers.