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

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    LEAD STYLET,MODELS 6505,6506,6507,6508

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MONDRIAN Lumbar Interbody Fusion Cage System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MAXIFLO, TAPERFLO

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BIOPSYS DRIVERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code KNW·June 8, 2006

    BIOPSYS DRIVERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATIA)·Product code KNW·June 8, 2006

    BIOPSYS DRIVERS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code KNW·June 7, 2006

    GORE® EXCLUDER® AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·June 27, 2016

    VIGILA 2CR 60/16 US

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVY·March 1, 2013

    ANEURX AAADVANTAGE STENT GRAFT SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code MIH·February 4, 2011

    CONSULTA CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 8, 2014

    LOGIC TIBIA PS MOD INSRT SZ 5 9MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·January 22, 2024