BEUDAMED
    11 results · 25ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    S.M.A.R.T. NITINOL STENT SYSTEM

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code FGE·January 28, 2016

    ADVANTA V12,COVERED STENT SYS,9X59X80

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code NIO·April 7, 2026

    1.5X5MM RAPIDFIRE SCREWS,5PK

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HWC·May 20, 2013

    PARADIGM INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code LZG·September 25, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·June 8, 2011

    ADVANTA V12 COVERED STENT SYSTEM

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORPORATION·Product code NIO·August 13, 2025

    ADVANTA V12 COVERED STENT

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code NIO·September 10, 2025

    ADVANTA V12,COVERED STENTSYS, 9X59X120

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code NIO·January 12, 2026

    ADVANTAV12,COVERED STENTSYS, 6X59X120

    FDA Adverse Event
    Malfunction ·ATRIUM MEDICAL CORPORATION·Product code NIO·January 12, 2026

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·November 26, 2019

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·November 8, 2019