BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    OMNIFIT II EPF HIP STEM SERIES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909115852·REVELATION DIAMOND 368-016C - 5 PACK

    FAST THERMOMETER MODELS ST713C AND ST713F

    FDA 510(k)
    FDA Class 2 ·General Hospital

    iNtuition-Structural Heart Module

    FDA 510(k)
    FDA Class 2 ·Radiology

    AIMING ARM FOR RETROGRADE STANDARD LOCKING

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code FZX·May 24, 2018

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·May 17, 2016

    MAVERICK2 MONORAIL PTCA CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LOX·April 11, 2007

    ASR ACETABULAR CUPS 54

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·November 29, 2010

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 3, 2014

    SEE H10

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDG·June 4, 2018