BEUDAMED
    10 results · 21ms · Sources: EU EUDAMED, US FDA

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    UNI/MONOPOLAR HF CABLE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    DynaNail Mini

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AMS ELEVATE ANTERIOR & APICAL PROLAPSE REPAIR SYSTEM WITH INTEPRO LITE

    FDA 510(k)
    FDA Class 3 ·Obstetrics/Gynecology

    AIRVANCE BONE SCREW (REPOSE) SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code LRK·March 3, 2014

    AIRVANCE BONE SCREW (REPOSE) SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED, INC·Product code LRK·March 29, 2013

    GIRAFFE T-PIECE

    FDA Adverse Event
    GE HEALTHCARE, LLC·Product code BTL·February 21, 2013

    POLARIS KIT SPVA B905S/BO19-10

    FDA Adverse Event
    Injury ·SOPHYSA·Product code JXG·January 21, 2011

    PLUM A+ UK WITH 3PIN

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·July 24, 2014

    AIRVANCE¿ THS SYSTEM - BONE SCREW WITH SUTURE

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code LRK·November 30, 2015

    AIRVANCE¿ THS SYSTEM - TOUNGE SUSPENSION KIT

    FDA Adverse Event
    Malfunction ·MEDTRONIC XOMED INC.·Product code LRK·October 2, 2015