BEUDAMED
    28 results · 72ms · 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 ×

    *

    FDA Adverse Event
    AESCULAP IMPLANT SYSTEMS, LLC·Product code HWA·November 17, 2014

    UP-ANGLED MICROPITUITARY

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS, LLC·Product code HTX·August 19, 2015

    VARADY VEIN HOOK

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS, LLC·Product code GAI·July 6, 2020

    AESCULAP VEGA KNEE SYSTEM

    FDA Adverse Event
    Injury ·AESCULAP IMPLANT SYSTEMS, LLC·Product code JWH·April 12, 2024

    TOTAL KNEE

    FDA Adverse Event
    Injury ·AESCULAP IMPLANT SYSTEMS, LLC·Product code JWH·October 23, 2018

    AESCULAP GRASPER

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS, LLC·Product code LXH·May 24, 2019

    AESCULAP, MONOPOLAR CORD

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS, LLC·Product code GEI·August 3, 2018

    ALLIS GRIPPER

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS, LLC·Product code GEN·November 14, 2016

    20 X 50 SCREW

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS, LLC·Product code HWC·October 24, 2012

    CASPAR DISTR PIN12MMSTET

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS, LLC·Product code LXH·January 16, 2019

    KERRISON

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS, LLC·Product code HAD·July 27, 2016

    AS UNIVATION XF

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS, LLC·Product code JWH·July 3, 2017

    CASPAR SELF-DRILLING DISTRACTION PIN

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS, LLC·Product code LXH·February 25, 2020

    AESCULAT COLUMBUS

    FDA Adverse Event
    Injury ·AESCULAP IMPLANT SYSTEMS, LLC·Product code JWH·March 1, 2021

    BI-POLAR CAUTERY

    FDA Adverse Event
    Malfunction ·AESCULAP IMPLANT SYSTEMS, LLC·Product code GEI·May 5, 2015

    TOTAL KNEE REPLACEMENT

    FDA Adverse Event
    Injury ·AESCULAP IMPLANT SYSTEMS LLC / B. BRAUN·Product code HSX·October 17, 2018

    AESCULAP VEGA

    FDA Adverse Event
    Injury ·B. BRAUN / AESCULAP IMPLANT SYSTEMS, LLC·Product code JWH·October 17, 2018

    AESCULAP VEGA

    FDA Adverse Event
    Malfunction ·B. BRAUN / AESCULAP IMPLANT SYSTEMS, LLC.·Product code HTG·October 17, 2018

    AESCULAP VEGA

    FDA Adverse Event
    Injury ·B. BRAUN / AESCULAP IMPLANT SYSTEMS, LLC·Product code JWH·October 17, 2018

    VEGA TOTAL KNEE

    FDA Adverse Event
    Injury ·AESCULAP IMPLANT SYSTEMS, LLC / B. BRAUN·Product code JWH·October 17, 2018