BEUDAMED
    6 results · 35ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    COBAS E 411 ANALYZER (RACK SYSTEM)

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·August 5, 2025

    COBAS 6000 E601 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·May 28, 2025

    MINICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·May 9, 2014

    TURBO ELITE LASER ABLATION CATHETER

    FDA Adverse Event
    Injury ·SPECTRANETICS CORPORATION·Product code MCW·October 23, 2012

    MAGIC 3 FEMALE INTERMITTENT CATHETER

    FDA Adverse Event
    Malfunction ·ROCHESTER MEDICAL CORP·Product code KOD·May 27, 2015

    COBAS E 411 ANALYZER (RACK SYSTEM)

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·January 27, 2025