BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    LEECO TESTOSTERONE DIAGNOSTIC KIT

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707028901·WEB 1ST MOLAR BANDS n.UL 12

    Hi-Pull

    FDA UDI
    LANCER ORTHODONTICS, INC.·00817573024070·HI-PULL STRIP BLUE EXTRA SMALL 5/PK

    NITIFLEX STAPES PROSTHESIS, DETROIT PISTON, SKARZYNSKI PISTON, ROBERSON STAPES PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    GUIDANT VASOVIEW ENDOSCOPIC VESSEL HARVESTING SYSTEM

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

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·November 19, 2024

    SURGICAL GUT SUTURE - CHROMIC

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAL·May 23, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·November 13, 2012

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Malfunction ·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·September 2, 2010

    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018