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

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    PADTAK PEDIATRIC DEFIB/CARDIOVERT/PACE/MONITOR-RADIOTRANSPARENT (2X2.25),MODEL 2602, PADTAK PEDIATRIC DEFIB/CARDIOVERT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Sklar

    FDA UDI
    SKLAR CORPORATION·10649111173233·MICRO RING FCP, DIAMOND 8.25 IN

    Trinias

    FDA UDI
    SHIMADZU CORPORATION·04540217058716·

    Double ENDOBUTTON Fixation Device

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO:MICROFUSE BONE VOID FILLER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AXIOM ARISTOS VX PLUS

    FDA Adverse Event
    Injury ·SIEMENS SHANGHAI MEDICAL EQUIPMENT LTD·Product code MQB·April 7, 2021

    ARCHITECT I2000SR ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING, INC.·Product code JJE·June 16, 2009

    FLOGARD

    FDA Adverse Event
    Malfunction ·SHARP CORPORATION OSAKA JAPAN·Product code FRN·February 28, 2013

    DEXTRUS 4137

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVZ·February 2, 2011

    ADULT CPB PACK

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP.·Product code DWF·July 3, 2014

    WALLSTENT? RP ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·July 21, 2025