BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    1X6YD, 2X6YD, 4X6YD ROLL BANDAGE

    FDA 510(k)
    FDA Unclassified ·Unknown

    ANTI-C (MONOCLONAL) SERIES 1

    FDA Adverse Event
    Malfunction ·IMMUCOR, INC.·Product code KSZ·August 7, 2008

    CUDDLE HEART -AUDITORY/VIBRATION DEVICE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SINGLE USE MANUAL RESUSCITATORS

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    NA

    FDA UDI
    Zimmer, Inc.·00889024078833·

    NA

    FDA UDI
    Zimmer, Inc.·00889024078826·

    ACCURUS 800CS

    FDA Adverse Event
    Injury ·ALCON- IRVINE TECHNOLOGY CENTER·Product code HQC·February 4, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·January 3, 2011

    MINICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·July 18, 2014