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

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    RESPI-NEB-AEROSOL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    AUDIFON SUENO CIC, AUDIFON SUENO S, AUDIFON SUENO T CIC, AUDIFON SUENO T S

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    DISPOSABLE STERILE INTERNAL DEFIBRILLATION PADDLES (SWITCHED-LARGE), DISPOSABLE STERILE INTERNAL DEFIBRILLATION PADDLES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PRECISION SPECTRA®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 23, 2014

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 13, 2012

    AED PLUS

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·September 2, 2010

    PLUG DRIVER

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code HXX·September 11, 2020

    PLUG DRIVER

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET SPINE INC.·Product code HXX·September 11, 2020

    Promote Quadra, Sterile EO, Model # / Part #: CD3221-36/100025054, 60019195; CD3223-36P/100013763; CD3239-40/100029115, 100029254, 100037181; CD3239-40Q/100029116, 100029244, 100037115

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018