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

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    Filters FDA Adverse Event ×

    COBAS E 402 ANALYTICAL UNIT

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·January 7, 2025

    COBAS E 801 ANALYTICAL UNIT

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·February 18, 2025

    COBAS E 801 ANALYTICAL UNIT

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·April 1, 2025

    COBAS E 402 ANALYTICAL UNIT

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·March 11, 2025

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 10, 2014

    MILLER/GALANTE POROUS TIBIAL PLATE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·October 12, 2012

    ANGIO-SEAL DEVICE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL PUERTO RICO, B.V.·Product code MGB·May 22, 2015