BEUDAMED
    14 results · 26ms · Sources: EU EUDAMED, US FDA

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    Evolve UniPolar Head

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    E.M.ADAMS, INC.

    FDA UDI
    E.M. ADAMS, INC.·B1211143184·

    MAXIM® VI KNEE SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00887868225963·

    MAXIM VI KNEE SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304205895·

    E.M Adams co, inc.

    FDA UDI
    E.M. ADAMS, INC.·18100013400800·CIRCUMCISION TRAY

    SILK'N FLASH N GO

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

    HEMOSIL RECOMBIPLASTIN

    FDA 510(k)
    FDA Class 2 ·Hematology

    ACL TOP

    FDA Adverse Event
    INSTRUMENTATION LABORATORY CO.·Product code GKP·May 13, 2005

    ACL TOP

    FDA Adverse Event
    Malfunction ·INSTRUMENTATION LABORATORY CO.·Product code GKP·July 21, 2005

    ACL ADVANCE

    FDA Adverse Event
    INSTRUMENTATION LABORATORY CO.·Product code JPA·April 22, 2005

    ROLLATOR

    FDA Adverse Event
    Injury ·MEDLINE INDUSTRIES, INC.·Product code ITJ·May 24, 2013

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 3, 2008

    STARCLOSE SE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·June 28, 2011

    TRUEMETRIX

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·June 28, 2017