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

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    MX960 REUSABLE PRESSURE TRANSDUCER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    C-STEM

    FDA UDI
    DEPUY INTERNATIONAL LTD·10603295237792·C-STEM Trial Stem Size 2

    Genesys Spine Apache® Lateral Lumbar Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MONO-CRAWFORD NASO-LACRIMAL INTUBATION DEVICE

    FDA 510(k)
    FDA Unclassified ·Unknown

    2520274-2013-10167

    FDA Adverse Event
    Malfunction ·SYNTHES·Product code KWQ·February 11, 2013

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·January 14, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 28, 2014

    FLEXOR PARALLEL URETERAL ACCESS SHEATH AND DILATORS

    FDA Adverse Event
    Injury ·COOK INC·Product code EZN·May 21, 2019