BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    MODIFICATION TO PREFERENCE PEDICLE SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPECTRA WAVEWRITER?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·July 10, 2025

    LIFESTYLES, CONTEMPO OR PRIVATE LABEL LARGE CONDOM

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

    POWDERED SYNTHETIC (YELLOW) VINYL PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    PIIC CLASSIC UPGRADE

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·January 24, 2024

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 29, 2013

    COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIECE FOLDABLE INTRAOCUL

    FDA Adverse Event
    Malfunction ·STAAR SURGICAL CO.·Product code HQL·April 5, 2011

    VERSASTEP REPO SHRT PWSHIELD 12MM RAD

    FDA Adverse Event
    Malfunction ·PONCE - USS·Product code GCJ·July 21, 2008