BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    INTERSEPT* OXYGEN GAS LINE FILTER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Modulus

    FDA UDI
    Nuvasive, Inc.·00887517023575·Modulus ALIF Trial, 12x34x28mm 25°SmDeep

    GLUCOSE REAGENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    Intelligent Wireless Fitness Apparatus (Model: AST-301, AST-302, AST-303)

    FDA 510(k)
    FDA Class 2 ·Neurology

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KXA·June 18, 2014

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·October 25, 2010

    LIFEVEST WCD 4000 SYSTEM

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

    EV3 Pipeline Flex Embolization Device with Flex Shield Technology

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

    Pipeline Flex Embolization Device

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