BEUDAMED
    7 results · 21ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    TRULIANT TIB IMP CR INS STD SZ 4, 15MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 5, 2022

    TRULIANT TIB IMP CR INS STD SZ 4, 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 5, 2022

    POWER MODULE F/TRS

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWE·March 14, 2013

    UNKNOWN ZIMMER CR FLEX FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code HSA·February 24, 2011

    SPACEMAKER STRUCTURAL BALLOON TROCAR

    FDA Adverse Event
    Malfunction ·PONCE - USS·Product code GCJ·February 22, 2008

    AS COLUMBUS REV F FEMUR ZEMENTIERT F5L

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code JWH·November 6, 2019

    13X100 MM 6.0 ML BD VACUTAINER® PLUS PLASTIC WHOLE BLOOD TUBE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO.·Product code JKA·July 26, 2017