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

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    D-SENSE

    FDA 510(k)
    FDA Class 2 ·Dental

    CONDOM (RUBBER) CONTRACEPTIVE

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

    NEOPROBE PORTABLE RADIOSCOPE DETECTOR

    FDA 510(k)
    FDA Class 1 ·Radiology

    HOPKINS TELESCOPE 0°, 5 MM, 29 CM

    FDA Adverse Event
    Malfunction ·KARL STORZ SE & CO. KG·Product code GCJ·May 16, 2025

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code DXY·February 11, 2013

    DURATA STS OPTIM ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·July 24, 2014