BEUDAMED
    10 results · 36ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    BIPOLAR MACRO FORCEPS D:5/ 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

    BIPOLAR MARYLAND DISS.FCPS 5MM 310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·March 9, 2015

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 29, 2014

    JAW INS. BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG.·Product code GEI·January 13, 2015

    MARYLAND GSP.FORCEPS FEN.5/310MM HF CON.

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·February 19, 2014

    JAW INS.BIP.MARYLAND DISS.FEN.5/310MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 13, 2015

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMERLY NELLCOR·Product code CBK·April 10, 2013

    ETHICON -J&J- ARTICULATING ENDOSCOPIC LINEAR CUTTER

    FDA Adverse Event
    Injury ·ETHICON ENDOMECHANICAL SURGICAL·Product code GDW·April 12, 2011

    PROLIEVE THERMODILATATION KIT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code MEQ·June 13, 2008

    MARYLAND GSP.FORCEPS FEN.5/310MM HF.CON.

    FDA Adverse Event
    Malfunction ·AESCULAP, INC.·Product code GEI·August 21, 2015