BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Adverse Event ×

    PRECISION NOVI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 30, 2020

    VNGD CR TIB BRG 14X63/67

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018

    VANGUARD CR ILOK FEM-RT 62.5

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018

    XIENCE SIERRA EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code NIQ·August 11, 2020

    TI OBA PLATE ANCHOR BRACKET DESIGN 5 HOLES

    FDA Adverse Event
    Malfunction ·SYNTHES ELMIRA·Product code OAT·April 22, 2013

    OXIMAX MAXA SENSOR

    FDA Adverse Event
    Death ·COVIDIEN, FORMERLY TYCO HEALTH·Product code DQA·June 27, 2008

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·April 18, 2011

    XIENCE XPEDITION 48 EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR·Product code NIQ·August 11, 2020

    XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR·Product code NIQ·February 5, 2024

    ECHELON ENDOPATH STAPLER

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 10, 2021