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

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    Catalyft™ LS Expandable Interbody System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SILTEX BECKER EXPANDER/MAMMARY PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR·Product code FTR·November 24, 1998

    MEDTRONIC STRATAVARIUS

    FDA 510(k)
    FDA Class 2 ·Neurology

    VARIAX 2 SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SILTEX BECKER EXPANDER/MAMMARY PROSTHESIS

    FDA Adverse Event
    Injury ·MENTOR·Product code FTR·November 24, 1998

    MULTIPORT TRANSCEIVER

    FDA Adverse Event
    Malfunction ·CABLETRON SYSTEMS·April 17, 1992

    UNKNOWN

    FDA Adverse Event
    Injury ·UNKNOWN·Product code FTR·July 1, 1992

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·November 10, 2014

    PROGRASP FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 23, 2013

    XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·November 22, 2015

    INSYTE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·January 22, 2026

    GEMINI

    FDA Adverse Event
    Death ·IMED·Product code FRN·July 16, 1993