BEUDAMED
    27 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    FR2

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS, HEARTSTREAM·Product code MKJ·September 16, 2010

    FR2

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS, HEARTSTREAM·Product code MKJ·September 16, 2010

    SYNCHRON® AMYLASE (AMY) REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JFJ·September 21, 2010

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·March 14, 2011

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code NEW·June 18, 2010

    FR2

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS, HEARTSTREAM·Product code MKJ·September 16, 2010

    SPRINT

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 9, 2010

    QUATTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·March 14, 2013

    ZIMMER LOCKING ONE-THIRD TUBULAR PLATE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code HRS·March 1, 2011

    PACESETTER, INC.

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC.·Product code DXY·February 15, 2008

    NIM® 3.0 INTERFACE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC·Product code GWF·September 27, 2017

    NIM® 3.0 INTERFACE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code GWF·September 1, 2017

    NIM® 3.0 INTERFACE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code GWF·October 11, 2017

    NIM® 3.0 INTERFACE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code GWF·August 28, 2017

    ACE

    FDA Adverse Event
    Malfunction ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code GAL·August 30, 2010

    NIM® 3.0 INTERFACE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code GWF·October 9, 2017

    NIM® 3.0 INTERFACE

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code GWF·October 9, 2017

    BD VACUTAINER® PLASTIC URINE COLLECTION CUP

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·June 22, 2018

    SURGISIS

    FDA Adverse Event
    Injury ·COOK BIOTECH·Product code FTM·April 14, 2016

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code NEW·January 12, 2011