BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Optilite C-Reactive Protein Reagent,Optilite C-Reactive Protein Calibrator,Optilite C-Reactive Protein Controls

    FDA 510(k)
    FDA Class 2 ·Immunology

    DREAMGARD REM-SOFT, DREAMGARD REM-LITE, DREAMGARD REM-ULTRA, DREAMGARD REM-MAX

    FDA 510(k)
    FDA Unclassified ·Unknown

    ACCOLADE II LASER

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

    HUMERAL HEAD 48.5X17

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 3015516266·Product code MBF·March 20, 2024

    ZOOM

    FDA Adverse Event
    Malfunction ·GUIDANT PUERTO RICO BV·Product code KRG·July 22, 2011

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·May 29, 2013

    ACAT 1 IAB PUMP ASSEMBLY

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DSP·September 19, 2008

    HAMMER

    FDA Adverse Event
    Malfunction ·EIT EMERGING IMPLANT TECHNOLOGIES GMBH·Product code LXH·February 11, 2020

    HAMMER

    FDA Adverse Event
    Malfunction ·EIT EMERGING IMPLANT TECHNOLOGIES GMBH·Product code MAX·February 11, 2020