BEUDAMED
    68 results · 24ms · Sources: EU EUDAMED, US FDA

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    COMPATIBILITY ECG TRUNK CABLES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    STERIS CORPORATION

    FDA registration
    STERIS CORPORATION·40 products·🇺🇸 United States

    MITEK BIOCRYL INTERFERENCE SCREWS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DYONICS CONTROL RF SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LB53 LIGHT HANDLE COVER

    FDA Adverse Event
    Malfunction ·STERIS CORPORATION - MONTGOMERY·Product code FTA·February 8, 2023

    HARMONYAIR

    FDA Adverse Event
    Malfunction ·STERIS CORPORATION·Product code FQO·October 6, 2023

    1043572-2003-00007

    FDA Adverse Event
    Other ·STERIS CORP - MONTGOMERY·Product code FQO·September 24, 2003

    1043572-2007-00015

    FDA Adverse Event
    Other ·Product code FQO·February 22, 2007

    1043572-1997-00014

    FDA Adverse Event
    Malfunction ·Product code FQO·June 19, 1997

    1043572-1997-00012

    FDA Adverse Event
    Malfunction ·Product code JEB·May 16, 1997

    1043572-2001-00006

    FDA Adverse Event
    Other ·STERIS CORP·Product code FQO·October 10, 2001

    1043572-2001-00007

    FDA Adverse Event
    Malfunction ·Product code FSE·October 10, 2001

    1043572-1999-00006

    FDA Adverse Event
    Malfunction ·December 28, 1999

    1043572-2012-00036

    FDA Adverse Event
    Malfunction ·STERIS CORPORATION·July 25, 2012

    1043572-2019-00020

    FDA Adverse Event
    Malfunction ·March 20, 2019

    1043572-2001-00003

    FDA Adverse Event
    Other ·STERIS CORP·Product code FQO·June 4, 2001

    1043572-2018-00052

    FDA Adverse Event
    Malfunction ·June 29, 2018

    1043572-2002-00005

    FDA Adverse Event
    Malfunction ·Product code FPO·November 1, 2002

    3085 SURGICAL TABLE

    FDA Adverse Event
    STERIS CORPORATION - MONTGOMERY·Product code FQO·August 20, 2012

    SPECTRA WAVEWRITER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 12, 2020