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

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    3 PORT ADAPTER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HEMASORB RESORBABLE HEMOSTATIC BONE PUTTY

    FDA 510(k)
    FDA Unclassified ·Unknown

    SONOACE SA-8000 DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    TRULIANT TIB IMP PS INSERT SZ 3 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 8, 2024

    DELTAPLUSH - CERECYTE MICROCOIL

    FDA Adverse Event
    Malfunction ·MICRUS ENDOVASCULAR, LLC·Product code HCG·January 14, 2013

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·November 12, 2010

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS·Product code LZG·July 3, 2014