BEUDAMED
    6 results · 27ms · 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 ×

    ERYTYPE S RH+K TYPE

    FDA Adverse Event
    Malfunction ·BIO-RAD MED DIAGNOSTICS GMBH·Product code KSZ·January 17, 2011

    MAMMOMAT INSPIRATION

    FDA Adverse Event
    Injury ·SIEMENS AG·Product code MUE·December 15, 2011

    PRODISC-C IMPLANT LARGE 6MM-STERILE

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MJO·April 2, 2013

    CARPENTIER-EDWARDS PERIMOUNT MAGNA PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·March 25, 2011

    COZMO INSULIN PUMP

    FDA Adverse Event
    Injury ·SMITHS MEDICAL MD, (FORMERLY DELTEC INC.)·Product code LZG·April 14, 2008

    3.0 RIO® ROBOTIC ARM - MICS

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·July 16, 2019