BEUDAMED
    11 results · 35ms · 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·March 18, 2025

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·March 18, 2025

    SERIES 7000 STANDARD TIBIA

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·August 29, 2012

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·April 3, 2025

    WALLACH ULTRA FREEZE

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code GEH·August 23, 2021

    RUSCH AGT NASAL PERFORMED ET TUBE, 7.0MM

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BSK·March 8, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

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

    SYNCHROMED

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·February 19, 2008

    IMPELLA 5.5

    FDA Adverse Event
    Malfunction ·ABIOMED, INC.·Product code OZD·June 12, 2025

    FISCHER CONE BIOP EX LG

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code HGI·May 1, 2018

    IMPELLA 5.5

    FDA Adverse Event
    Injury ·ABIOMED, INC.·Product code OZD·June 19, 2025