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

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    Filters Regulation: Us FDA ×

    MEDTRONIC BIO-MEDICUS FEMORAL CANNULA/INTRODUCER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MICRO-COLL COLLAGEN DERMAL WOUND SPRAY

    FDA 510(k)
    FDA Unclassified ·Unknown

    VINYL EXAMINATION GLOVES(MFG:KAO YING INDUSTRIAL)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ENDOPATH** XCEL*

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·December 14, 2010

    OT VERIO TEST STRIPS

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 10, 2014

    SITTER II

    FDA Adverse Event
    Malfunction ·J. T. POSEY CO.·Product code KMI·December 14, 2012

    EVOLUTION DUODENAL CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code MUM·April 25, 2014

    ev3 Pipeline Flex Embolization Device. For neurological endovascular use.

    FDA Enforcement
    Class I ·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·April 1, 2020