BEUDAMED
    9 results · 28ms · Sources: EU EUDAMED, US FDA

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    H-TRONPLUS V100 INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·DISETRONIC MEDICAL SYSEMS, INC.·Product code LZG·August 14, 2003

    GREENLIGHT MOXY FIBER OPTIC

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSEMS, INC·Product code GEX·November 1, 2018

    Merit Medical Sysems, Inc. Pressure Infusor Bag MERITMEDICAL 500 ml Pressure Infusor Bag CATALOG NUMBER PIB500 Used to apply pressure to a sealed bag of sterile fluid.

    FDA Recall
    Terminated ·Merit Medical Systems, Inc.·Product code KZD·September 29, 2009

    OEC 9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSEMS INC·Product code JAA·February 11, 2010

    8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSEMS, INC·Product code JAA·June 30, 2007

    GUIDANT - TETRA STENT

    FDA Adverse Event
    Other ·GUIDANT ADVANCED CARDIOVASCULAR SYSEMS, INC.·Product code MAF·January 31, 2001

    Elekta MONACO RTP Sytem, radiation treatment planning software system - Product Usage: The Monaco system is used to make treatment plans for patients with prescriptions for external beam radiation therapy. The

    FDA Recall
    Open, Classified ·Elekta Inc·Product code MUJ·April 16, 2020

    AQURE basic sytem, FLEXLINK, REF 933-599, Version: 2.3.3 (17), CE IVD, Rx Only, UDI: (01)05700699335999 Intended use: The AQURE system is intended to let you manage analytical devices and operator profiles.

    FDA Recall
    Terminated ·Radiometer Medical ApS Akandevej 21 Bronshoj Denmark·Product code OUG·August 8, 2019

    NIR ON RANGER

    FDA Adverse Event
    Injury ·SCIMED LIFE SYSEM, INC./A SUBSIDIARY OF BOSTON SCIENTIFIC CORP·Product code MAF·September 28, 1998