BEUDAMED
    39 results · 22ms · Sources: EU EUDAMED, US FDA

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    WOUND MEASURING & MONITORING DEVICE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    ArgenIS

    FDA UDI
    ARGEN CORPORATION, THE·D818131596·MUA ZS NP 2.0GH Str

    TOTAL SHOULDER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    KIMBERLY-CLARK PURPLE NITRILE POWDER-FREE EXAM GLOVE (CHEMOTHERAPY GLOVE) AND KIMBERLY-CLARK PURPLE NITRILE XTRA POWDER-

    FDA 510(k)
    FDA Class 1 ·General Hospital

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·August 12, 2015

    CAIMAN DISP. INSTR. ARTICULAT. D:12/240MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code GEI·November 11, 2014

    CAIMAN DISP. INSTR. ARTICULAR D-12/240MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·May 6, 2014

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/360MM

    FDA Adverse Event
    Malfunction ·B. BRAUN SURGICAL S.A.·Product code GEI·March 21, 2014

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code GEI·December 12, 2014

    CAIMAN DISP.INSTR.NON ARTICUL. D: 5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/360 MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·June 17, 2015

    CAIMAN DISP. INSTR. ARTICULAT. D:12/240MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code GEI·November 11, 2014

    CAIMAN DISP. INSTR. ARTICULAT. D:12/240MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code GEI·November 11, 2014

    CAIMAN DISP, INSTR. ARTICULAR. D:12/240MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·March 12, 2014

    CAIMAN DISP.INSTR.NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GEI·November 1, 2015

    CAIMAN DISP. INSTR. NON ARTICUL.D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·March 12, 2014

    CAIMAN DISP. INSTR. NON ARTICUL. D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AP & CO. KG·Product code GEI·March 27, 2015

    CAIMAN DISP.INSTR.NON ARTICUL. D:5/360MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·March 12, 2014

    CAIMAN DISP.INSTR.ARTICULAT.D:12/240MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO KG·Product code GEI·April 6, 2015

    SPRINT QUATTRO

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·June 16, 2011