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

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    BRANEMARK SYSTEM BALL ATTACHMENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    KD-322 SEMI AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FD TENS 2090, FD TENS 2095

    FDA 510(k)
    FDA Class 2 ·Neurology

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·RICE CREEK MANUFACTURING·Product code DXY·February 9, 2013

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·January 7, 2011

    COYOTE? ES

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LIT·July 23, 2014

    Azurion 7 M20; System Code: (1)722079, (2)722224, (3)722234, (4)722282 (OUS only);

    FDA Enforcement
    Class II ·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·April 8, 2026