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

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    Patient Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CDC ZIRCONIA BLANKS

    FDA 510(k)
    FDA Class 2 ·Dental

    LIFEPAK 12

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    LIFEPAK(R) 20 DEFIBRILLATOR/MONITOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code LDD·December 4, 2012

    LIFEPAK® 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·February 6, 2019

    LIFEPAK(R) 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·October 25, 2019

    MECHANICAL (MANUAL) WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code IOR·October 22, 2014

    VA LOCKSCR Ø2.4 SELF-TAP L16 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·June 27, 2013

    B.BRAUN

    FDA Adverse Event
    Injury ·B.BRAUN MED INC.·Product code NGT·March 6, 2008