BEUDAMED
    7 results · 31ms · 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 ×

    STAT DL 9.5 FR. 40 CC. IAB

    FDA Adverse Event
    Malfunction ·DATASCOPE CORPORATION·Product code DSP·January 15, 1998

    MIS INSTRUMENTATION LATERAL ALIGNMENT FRAME

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code LXH·June 24, 2016

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·May 8, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 17, 2012

    RESTORE SMALL DBS EXTENSION

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·August 12, 2010

    COBAS AMPLIPREP / COBAS AMPLICOR HCV TEST, V2.0 CE-IVD

    FDA Adverse Event
    ROCHE MOLECULAR SYSTEMS·Product code MZP·December 19, 2012

    COBAS AMPLIPREP / COBAS AMPLICOR HCV TEST, V2.0 CE-IVD

    FDA Adverse Event
    ROCHE MOLECULAR SYSTEMS·Product code MZP·December 19, 2012