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

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    Filters Regulation: Us FDA ×

    EXTENDED SHELF LIFE FOR INTERSEPT* ARTERIAL 20/40

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Modulus

    FDA UDI
    Nuvasive, Inc.·00887517023582·Modulus ALIF Trial, 6x34x28mm 30°SmDeep

    MEDTRONIC MODEL 3797 ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Neurology

    DLMS-ZIRBLOCKS

    FDA 510(k)
    FDA Class 2 ·Dental

    OT ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 18, 2014

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·October 25, 2010

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·November 12, 2012

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021