BEUDAMED
    7 results · 20ms · 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 ×

    LEGEND FOOTED ATTACHMENT

    FDA Adverse Event
    Malfunction ·MDT POWERED SURGICAL SOLUTIONS·Product code HBB·May 15, 2014

    ATTAIN STARFIX

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code OJX·October 31, 2012

    CROSSER RECANALIZATION CATHETER

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code DQY·May 22, 2015

    OSS 7CM SEGMENTAL FEMORAL RT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·September 9, 2020

    OSS CEMENTED IM STEM 13X150

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·September 9, 2020

    SMR CONNECTOR SMALL STD

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code KWS·March 31, 2022

    REFOBACIN BONE CEMENT R 1X40G

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code MBB·October 12, 2020