BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    TD-5010 Lancing Device and TD-5084 Sterile Lancets

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

    TALOS° HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1676221419070·

    TALOS° HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1676221419000·

    TALOS° HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1676221419150·

    AART MALAR IMPLANT

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

    Gingi-Aid Gel

    FDA 510(k)
    FDA Unclassified ·Unknown

    OSSEOTITE IMPLANT 4 X 15MM

    FDA Adverse Event
    Injury ·ZIMVIE US CORP LLC·Product code DZE·November 26, 2025

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·November 3, 2014

    LIGASURE ADVANCE PISTOL GRIP

    FDA Adverse Event
    Malfunction ·COVIDIEN LP·Product code GEI·June 28, 2013

    X8000 LIGHTSOURCE

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY SAN JOSE·Product code FCW·August 16, 2011