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

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    Filters Regulation: Us FDA ×

    MINNE TIES MMF Suture System

    FDA 510(k)
    FDA Class 2 ·Dental

    Adler Instrument Company

    FDA UDI
    Adler, Inc.·00810123203338·Slotted "U" Bracket,

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776115876·Slotted U Bracket

    MODIFIED MERCI RETRIEVER, MODEL 90050

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MTA ANGELUS

    FDA 510(k)
    FDA Class 2 ·Dental

    LINER: VERSAFITCUP CC TRIO FLAT PE HC LINER 28 / C

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·April 6, 2021

    FLOSEAL

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code LMF·July 6, 2011

    STENOSCOP

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 6, 2013

    COBAS 6000 E601 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·October 10, 2014