BEUDAMED
    5 results · 35ms · 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 ×

    LONG NAIL KIT R2.0, TI, RIGHT GAMMA3 11X360MM X 1

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code JDS·October 11, 2012

    ESSURE

    FDA Adverse Event
    Injury ·BAYER PHARMA AG·Product code HHS·May 21, 2019

    OT VERIO IQ METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 19, 2014

    ROD

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HSB·December 21, 2012

    AQUAMANTYS 2.3

    FDA Adverse Event
    Malfunction ·SALIENT SURGICAL TECHNOLOGIES·Product code GEI·September 17, 2010