BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    M9/M9CV/M9T Diagnostic Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    HERACERAM ZIRKONIA

    FDA 510(k)
    FDA Class 2 ·Dental

    BRAVO PH MONITORING SYSTEM AND ACCESSORIES

    FDA 510(k)
    FDA Class 1 ·Gastroenterology, Urology

    PENUMBRA SYSTEM ACE 64 REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·July 17, 2015

    CUP: VERSAFITCUP ACETABULAR SHELL Ø 52

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·October 18, 2022

    ALIGN TO URETHRAL SUPPORT SYSTEM

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON)·Product code FTL·June 5, 2013

    AXSYM RUBELLA IGG ANTIBODY

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code LFX·September 10, 2008

    GEMSTR 7 THPY ALT ST

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·June 27, 2011

    WALLFLEX? BILIARY TRANSHEPATIC

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code FGE·August 21, 2012