BEUDAMED
    6 results · 28ms · Sources: EU EUDAMED, US FDA

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    MAXI-VAC TM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    RESTORIS MULTICOMPARTMENTAL KNEE (MCK) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COLPOSCOPE (DYNATECH COLPOSCOPE-MODEL I

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE SUZHOU·Product code CAW·May 5, 2014

    CAPSURE Z NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 15, 2012

    CE INTERMATE LV 50, 24 PACK, 50126

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·August 10, 2010