BEUDAMED
    10 results · 23ms · Sources: EU EUDAMED, US FDA

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    TEMPERATURE MONITOR

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ALIF

    FDA UDI
    Nuvasive, Inc.·00887517622167·ALIF Ti Interfixated Imp, 10x34x24 25°

    ECG-1250A SERIES CARDIOFAX S AND ECG-1350A SERIES CARDIOFAX M

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Flexor Ureteral Access Sheath and Flexor Parallel Rapid Release Ureteral Access Sheath

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    LAP-BAND AP ADJUSTABLE GATRIC BANDING SYSTEM (STANDARD)

    FDA Adverse Event
    Malfunction ·ALLERGAN·Product code LTI·January 2, 2014

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·October 4, 2012

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·July 22, 2010

    FLEXOR URETERAL ACCESS SHEATH AND DILATORS

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FED·January 3, 2020

    FLEXOR URETERAL ACCESS SHEATH AND DILATORS

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FED·January 2, 2020

    FLEXOR URETERAL ACCESS SHEATH AND DILATORS

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FED·January 7, 2020