BEUDAMED
    11 results · 35ms · Sources: EU EUDAMED, US FDA

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    DASH 1000 PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970545·anteriors; shade BL3; mould UBL

    MEGA PLUS MIS SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809665585936·MIS Fenestrated Screw, Ø10.5 x 45mm, Ø6.0mm Rod

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111339103·CHISEL CORN CVD EDGE SPOON

    K-Y BRAND WARMING LIQUID

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Automatic Wrist Bluetooth Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SEE H10

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code NBC·April 18, 2013

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·June 10, 2014

    PK DISSECTING FORCEPS

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·February 20, 2013

    TECNIS CL

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL OPTICS·Product code HQL·January 25, 2011

    CERAMIC ELECTRODE TIP L-HK F/GK372R

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code GEI·July 5, 2019