BEUDAMED
    10 results · 18ms · Sources: EU EUDAMED, US FDA

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    K-LOK CATHETER SECUREMENT DEVICE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    N/A

    FDA UDI
    Tyber Medical, LLC·M695M9302250·

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515237728·Repercussion Free Mallet, 21 oz., 11 1/2"

    QUASAR C100, BABY QUASAR PLUS, QUASAR MD PLUS; WRINKLE REDUCTION DEVICE

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

    DynaFlex Clear Brackets & Buttons

    FDA 510(k)
    FDA Class 2 ·Dental

    HU-FRIEDY PERMA SHARP SUTURES

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code GAR·May 26, 2010

    COREVALVE TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·March 20, 2019

    FENESTRATED BIPOLAR FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·January 25, 2013

    Z-5 ATRIOSEPTOSTOMY CATHETER

    FDA Adverse Event
    Malfunction ·NUMED CANADA, INC.·Product code DQO·November 18, 2010

    CAPSUREEPI

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTB·July 11, 2014