BEUDAMED
    6 results · 33ms · Sources: EU EUDAMED, US FDA

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    HOLDER, NEEDLE

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    PHILIPS AVENT CLASSIC STAGE 2 AND 3 TEETHER, MODEL SCF882/01, SCF884/01, PHILIPS AVENT ANIMAL STAGE 2 AND 3 TEETHER,

    FDA 510(k)
    FDA Class 2 ·Dental

    MitraClip G4 Steerable Guide Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ADVIA 1800

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·June 24, 2014

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·December 28, 2012

    TANGORS POSTERIOR SYSTEM

    FDA Adverse Event
    Injury ·ULRICH GMBH & CO. KG·Product code NKB·October 29, 2010