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

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    Filters FDA Adverse Event ×

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 7, 2014

    REUSABLE CANNULAS -

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW ENDOSCOPY·Product code NBH·November 5, 2010

    PHILOS SR COATED

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVZ·November 21, 2012

    COBAS E 411 ANALYZER (RACK SYSTEM)

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·April 1, 2026