BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    AS/3 NMT MODULE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ZAVATION

    FDA UDI
    Zavation LLC·00842166190450·Polyaxial Screw 5.0x26

    ACCULEVEL PHENYTOIN TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    DUAL FLEX NON-LATEX

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    COULTER® ACT DIFF 2 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC·Product code GKZ·December 7, 2010

    ARTICULEZE M HEAD 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code JDI·February 11, 2013

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011

    DRIVE SHAFT-MINIMUM 520MM LENGTH-FOR USE WITH RIA

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HTO·July 24, 2014