BEUDAMED
    6 results · 46ms · Sources: EU EUDAMED, US FDA

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    Infinity Delta Portable Patient Monitor. Draeger Medical Systems, Inc. Portable monitor used to monitor vital signs of neonatal, pediatric, and adult patients for bedside and transport applications.

    FDA Recall
    Terminated ·Draeger Medical Systems, Inc.·Product code MHX·July 29, 2011

    Infinity Gamma X XL Portable Patient Monitor. Draeger Medical Systems, Inc. Portable monitor used to monitor vital signs of neonatal, pediatric, and adult patients for bedside and transport applications.

    FDA Recall
    Terminated ·Draeger Medical Systems, Inc.·Product code MHX·July 29, 2011

    ACUSON Sequoia Diagnostic Ultrasound System, general purpose Diagnostic Ultrasound system. Siemens Medical Solutions USA, Inc., Mountain View, CA

    FDA Recall
    Terminated ·Siemens Medical Solutions USA, Inc.·Product code IYN·September 25, 2007

    Liver Access and Biopsy Needle Set Biopsy needle kit Intended for use in obtaining liver histology samples via a jugular vein approach.

    FDA Recall
    Terminated ·Cook Inc.·Product code FCG·April 15, 2016

    Infusable and Infusa Scan Single Patient Use Pressure Infusors; Vital Signs Inc. A pressure infusor for an IV bag is a device consisting of an inflatable cuff which is placed around and IV bag. When the device is inflated, it increases the pressure on the IV bag to assist the infusion of the fluid.

    FDA Recall
    Terminated ·GE Healthcare, LLC·Product code KZD·March 4, 2011

    TomoMobile, Hi-Art System, H-0000-0003, TomoTherapy 1240 Deming Way, Madison, WI 53717 The TomoTherapy HI-ART System is intended to be used as an integrated system for the planning and precise delivery of radiation therapy, stereotactic radiotherapy, or stereotactic radiosurgery to tumors or other targeted tissues while minimizing the delivery of radiation to vital healthy tissue. The megavoltage x-ray radiation is delivered in a rotational, non-rotational, modulated (IMRT), or non modulated (non-IMRT/three dimensional conformal) format in accordance with the physician approved plan.

    FDA Recall
    Terminated ·Accuray Incorporated·Product code MUJ·July 7, 2011