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

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    ULTRATHIN URETEROSCOPES

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

    URETEROSCOPE, 8,6/9,8 FR. X 430 MM, 7°, 6,4 FR. CHANNEL, WITH A0396

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code FGB·December 16, 2016

    SLI Endoprobe, SLI DENT Bare Fiber, SLI HO Bare Fiber, SLI HCS Bare Fiber, SLI Lateral Firing Fiber

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

    VENTRI

    FDA 510(k)
    FDA Class 2 ·Radiology

    N/A

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO·Product code NVZ·February 9, 2013

    PUMP MMT-522LWWL PRDGM INS CL EN LN

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·December 28, 2010

    INFINITI VISION SYSTEM OZIL

    FDA Adverse Event
    Injury ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·July 2, 2014

    ULTRACLEAN ELECTRODE 1"BLADE EXTENDED INSULATION

    FDA Adverse Event
    Malfunction ·CONSOLIDATED MEDICAL EQUIPMENT·Product code GEI·January 3, 2020

    Breast Augmentation Pack, part number AMS1786(A Breast Augmentation Pack, part number AMS2790(A Breast Augmentation Pack, part number AMS3324(B Breast Augmentation Pack, part number AMS4382 Breast Augmentation Pack, part number AMS4382(A Breast Augmentation Pack, part number AMS4382(B Breast Augmentation Pack, part number AMS4392 Breast Augmentation Pack, part number PSS3430

    FDA Enforcement
    Class II ·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017