BEUDAMED
    6 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    DILATOR, VESSEL, FOR PERCUTANEOUS CATHETERIZATION

    FDA Adverse Event
    Injury ·ANGIODYNAMICS, INC.·Product code DRE·April 13, 2026

    PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA, INC.·Product code LWP·June 10, 2014

    CAREASSIST BED

    FDA Adverse Event
    Malfunction ·HILL-ROM PLUVIGNER·Product code FNL·November 5, 2012

    SYMBIQ SINGLE CHANNE

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code FRN·September 27, 2010

    MINI STICK MAX COAXIAL MICROINTRODUCER KIT

    FDA Adverse Event
    Injury ·ANGIODYNAMICS, INC.·Product code DRE·May 11, 2026

    THREE PEG PATELLA 38MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·October 10, 2024