BEUDAMED
    7 results · 44ms · Sources: EU EUDAMED, US FDA

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    Esteya

    FDA 510(k)
    FDA Class 2 ·Radiology

    STRYKER IVAS BALLOON CATHETER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POWDER FREE BLUE LATEX EXAMINATION GLOVE, NON-STERILE (PROTEIN CONTENT LABELING)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PINN MAR +4 NEUT 36IDX54OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·October 27, 2008

    PINNACLE MTL INS NEUT40IDX56OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·August 12, 2011

    TI NUT 11MM WIDTH ACROSS FLATS

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code KWP·July 9, 2013

    Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System, labeled as EMBLEM MRI S-ICD Pulse Generator

    FDA Enforcement
    Class II ·Ongoing·Boston Scientific Corporation·September 25, 2019