BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    SUTURE REMOVAL KIT

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110997·DOUBLE PLASTIC STERILIZATION CASE

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110980·STERILIZING CASE PLASTIC LARGE

    Restore

    FDA UDI
    KEYSTONE DENTAL, INC.·D768R92034048K0·UCLA Screw

    MODIFICATION TO HI-TORQUE WHISPER LS AND MS GUIDE WIRES WITH HYDROCOAT HYDROPHILIC COATING

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VENUS FACET SCREW SYSTEM

    FDA 510(k)
    FDA Unclassified ·Unknown

    STARCLOSE SE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·AV-REDWOOD CITY·Product code MGB·December 10, 2010

    ASR UNI FEMORAL IMPL SIZE 43

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 17, 2013

    AUTOPULSE® RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code DRM·July 8, 2014