BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    TITANIUM CATHETER EXTENDER

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

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909107852·REVELATION DIAMOND 860-010M - 5 PACK

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756377638·BREAST PACK

    KALARE DIAGNOSTIC X-RAY TABLE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    KSEA DION-GRACIA SET

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SILK SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAP·November 11, 2020

    TOSHIBA Kalare Diagnostic X-Ray System K110785

    FDA Recall
    Terminated ·Toshiba American Medical Systems Inc·Product code JAA·April 3, 2013

    EASYTRAK 3

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code OJX·January 11, 2013

    PDS II (POLYDIOXANONE) SUTURE

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code NEW·November 22, 2010

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code ILS·July 2, 2014

    TOSHIBA Kalare Diagnostic X-Ray System K110785

    FDA Enforcement
    Class II ·Terminated·Toshiba American Medical Systems Inc·July 17, 2013