BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    QM300 ALBUMIN ANTIBODY PACK

    FDA 510(k)
    FDA Class 2 ·Immunology

    GISH SVR SOFT VENOUS RESERVOIRS WITH HA COATING

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Tumark for Eviva, Tumark for Brevera

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

    OEC Uroview 2800 with Dual Monitor Option, fluoroscopic x-ray system, Model Numbers: 882082-01, 882082-02, 886765-01, GE Healthcare, Surgery, Salt Lake City, UT.

    FDA Recall
    Terminated ·GE OEC Medical Systems, Inc·Product code JAA·January 15, 2007

    FEMORAL STEM PRESS-FIT COLLARLESS 12/14 NECK TAPER STANDARD BODY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·October 13, 2022

    AFN Ø11 R L420 TAN

    FDA Adverse Event
    Malfunction ·SYNTHES BETTLACH·Product code JDS·June 18, 2014

    RADIAL JAW 3 BIOPSY FORCEPS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA·Product code FCL·October 25, 2010

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·November 7, 2012

    OEC Uroview 2800 fluoroscopic x-ray system with 3 Phase Power Distribution Box option (Wonder Box) , Model Numbers: 882082-01, 882082-02, 886765-01, GE Healthcare, Surgery, Salt Lake City, UT.

    FDA Recall
    Terminated ·GE OEC Medical Systems, Inc·Product code JAA·January 15, 2007