BEUDAMED
    11 results · 33ms · Sources: EU EUDAMED, US FDA

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    DIA-SPEC

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

    FAC-4 - Class B 21 Lawson - 4 Shelf Cabinet

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588620862·FAC-4 - Class B 21 Lawson - 4 Shelf Cabinet

    THERMAL LIGATING SHEARS

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

    AIM-V (R) MEDIUM, MODEL 087-0112

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

    ENDOWRIST ONE VESSEL SEALERINSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·May 20, 2014

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·October 9, 2012

    BRAVO

    FDA Adverse Event
    Malfunction ·GIVEN IMAGING LTD.·Product code FFT·August 22, 2010

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·May 23, 2018

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·May 23, 2018

    BD MAX¿ SYSTEM, BD MAX¿ INSTRUMENT

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code OOI·April 7, 2022

    BD SARS-COV-2 REAGENTS FOR BD MAX¿ SYSTEM

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code QJR·April 27, 2022