Profile: Fluke Biomedical manufactures biomedical test & simulation products, including electrical safety testers, patient simulators, performance analyzers, and fully-integrated & automated performance testing and documentation systems. Our product 7600 Double Check Pro is a portable, easy-to-use, daily check device for therapy beam quality assurance. Ten ion chambers are positioned to simultaneously check beam constancy, symmetry, flatness, and energy constancy. Nine ion chambers are used for the verification of flatness, symmetry, and dose constancy while a special filtered ion chamber provides energy constancy information. The Double Check Pro consists of a detector array and software for performing linear accelerator quality assurance using physician preferred air ion chamber technology for dose measurement, avoiding the radiation damage issues of diode detectors. Windows® CE based software acquires beam profile data from the detector array. The beam profile is displayed numerically or graphically. Beam profile analysis such as flatness and symmetry is performed and is saved in a database resident on the unit, facilitating daily, weekly, yearly checks, aiding in following the guidelines in TG-40. The data is also available for correlation to TG-51 data.

The company is ISO 9001, CE certified. NYSE:DHR (SEC Filings)

FDA Registration Number: 2921581

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• Pacemaker Generator Function Analyzer (FDA Code: DTC / 870.3630) A pacemaker generator function analyzer is a device that is connected to a pacemaker pulse generator to test any or all of the generator's parameters, including pulse duration, pulse amplitude, pulse rate, and sensing threshold.

• Pediatric Pulse Oximeter

• Peristaltic Infusion Pump (FDA Code: FRN / 880.5725) An infusion pump is a device used in a health care facility to pump fluids into a patient in a controlled manner. The device may use a piston pump, a roller pump, or a peristaltic pump and may be powered electrically or mechanically. The device may also operate using a constant force to propel the fluid through a narrow tube which determines the flow rate. The device may include means to detect a fault condition, such as air in, or blockage of, the infusion line and to activate an alarm.

• 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.

• Pocket Pc Bar code Reader

• Portable Bar Code Reader

• Portable Leakage Current Alarm (FDA Code: DSM / 870.2640) A portable leakage current alarm is a device used to measure the electrical leakage current between any two points of an electrical system and to sound an alarm if the current exceeds a certain threshold.

• Portable Pulse Oximeter

• Product Development, Pulse Oximeter

• Protective Wear

• 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

• Pulse Oximeter with Artefact Suppression and one channel ECG

• Pulse Oximeter with Charger

• Pulse Oximeter with One Channel ECG

• Pulse Oximeters

• 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 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 Protective Curtain (FDA Code: IWQ / 892.6500)

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

• Radiologic Patient Cradle (FDA Code: KXH / 892.1830) A radiologic patient cradle is a support device intended to be used for rotational positioning about the longitudinal axis of a patient during radiologic procedures.

• Radiological Quality-Assurance Instrument (FDA Code: LHO / 892.1940)

• Radiology Computer Software

• Radionuclide Dose Calibrator (FDA Code: KPT / 892.1360) A radionuclide dose calibrator is a radiation detection device intended to assay radionuclides before their administration to patients.

• Radionuclide Test Pattern/Phantom (FDA Code: JAR / 892.1420) A radionuclide test pattern phantom is a device that consists of an arrangement of radiopaque or radioactive material sealed in a solid pattern intended to serve as a test for a performance characteristic of a nuclear medicine imaging device.

• Reflectance Densitometer/Scanner (FDA Code: JQT / 862.2400) A densitometer/scanner (integrating, reflectance, thin-layer chromatography, or radiochromatogram) for clinical use is device intended to measure the concentration of a substance on the surface of a film or other support media by either a photocell measurement of the light transmission through a given area of the medium or, in the case of the radiochromatogram scanner, by measurement of the distribution of a specific radio-active element on a radiochromatogram.

• Respiration Simulator

• Reusable Pulse Oximeter Finger Sensor Repair

• Reusable Pulse Oximeter Finger Sensors

• Reusable Pulse Oximeter Sensors

• Signal Isolation System (FDA Code: DRJ / 870.2600) A signal isolation system is a device that electrically isolates the patient from equipment connected to the commercial power supply received from a utility company. This isolation may be accomplished, for example, by transformer coupling, acoustic coupling, or optical coupling.

• Soft Tip Reusable Pulse Oximeter Sensor

• Spo2 Pulse Oximeter

• Surgery Indirect Blood Pressure Monitor

• Symbol Bar Code Reader

• Tabletop Digital Pulse Oximeter

• Therapeutic X-Ray System (FDA Code: JAD / 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.

• Thigh Blood Pressure Inflation Cuffs

• Used Pulse Oximeters

• Wireless Bar Code Reader

• X-Ray Accessories, Leaded Aprons (FDA Code: EAJ / 892.6500)

• X-Ray Protective Wear