BEUDAMED
    7 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·January 26, 2025

    CRE 18-20MM 8CM F/G

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORK LTD.·Product code KNQ·March 21, 2007

    RANGER MONITOR W/SNAPS, LARGE & POWER SUPPLY

    FDA Adverse Event
    Malfunction ·VERATHON MEDICAL (CANADA) ULC.·Product code CCW·February 14, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·February 24, 2011

    RESTORE PRIME

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·February 19, 2008

    LEEP SYSTEM 1000 ESU GEN

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code HGI·September 20, 2021

    17G WALLACE OOCYTE RCVRY

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code MQE·September 4, 2022