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

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    AcQGuide® VUE Steerable Sheath

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    24M - Southwest Gas Corp

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588010441·24M - Southwest Gas Corp

    MADETT

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ILLUMIGENE GROUP B STREPTOCOCCUS CARROT BROTH CLAIM

    FDA 510(k)
    FDA Class 1 ·Microbiology

    CERTAIN® GOLD-TITE® HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·July 26, 2019

    U1105 S1000 TINA HD WITH HIBP

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE CORPORATION·Product code FKP·November 4, 2008

    PRECISION

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 23, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 11, 2013

    LIBERTY CYCLER SET, SINGLE CONN./EXT. DL

    FDA Adverse Event
    Malfunction ·REYNOSE MANUFACTURING·Product code FKX·August 19, 2011