BEUDAMED
    10 results · 38ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO NUVASIVE LATERAL PLATE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VERTE-STACK ANATOMIC PEEK STRUT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code MQP·May 5, 2020

    SCREENERS OPIATES TEST DRUGSCREEN DIP OPIATES TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    CRANIAL MOLDING ORTHOSIS

    FDA 510(k)
    FDA Class 2 ·Neurology

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code CBK·April 16, 2013

    INFORMATION CENTER NETWORK DATABASE

    FDA Adverse Event
    Death ·PHILIPS HEALTHCARE·Product code MHX·April 19, 2011

    GE OEC 9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·July 9, 2008

    3.5MM TI CANCELLOUS POLYAXIAL SCREW 22MM

    FDA Adverse Event
    Injury ·SYNTHES PRODUKTIONS GMBH·Product code NKG·February 8, 2018

    LOCKSCR SYNAPSE TAN

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code NKG·February 15, 2018

    LOCKSCR SYNAPSE TAN

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code NKG·February 15, 2018