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

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    Filters Regulation: Us FDA ×

    VENTRICULAR CATHETER SET

    FDA 510(k)
    FDA Class 2 ·Neurology

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471149878·K-WIRE - DOUBLE TROCAR FULLY THREADED 2.0mm DIA...

    InTRAkit

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VERESS CANNULA AND MODULAR VERESS CANNULA

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

    DRILL SLEEVE F. SOLID STEPDRILL

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·February 23, 2012

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·May 7, 2022

    PENTAX

    FDA Adverse Event
    Malfunction ·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDS·October 12, 2022

    INFERIOR END PLATE MEDIUM-STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES BRANDYWINE·Product code MJO·February 14, 2013

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·January 17, 2011

    CABLE TENSIONER

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code LXH·July 28, 2014

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·February 6, 2017