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

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    WIRELESS/WIRED FDR D-EVO FLAT PANEL DETECTOR

    FDA 510(k)
    FDA Class 2 ·Radiology

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

    FDA Adverse Event
    Malfunction ·AESCULAP, INC.·Product code GEI·March 4, 2015

    MATHIEU-OLSEN NEEDLE HOLDER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896053243·MATHIEU-OLSEN NEEDLE HOLDER TUNGSTEN CARBIDE SE...

    Pointe Scientific, Inc.

    FDA UDI
    HORIBA INSTRUMENTS INCORPORATED·00811727013330·IgE for the quantitative determination of Immun...

    Novo Surgical

    FDA UDI
    NOVO SURGICAL, INC.·G586E1035960·brown (dean) cotton applicator, triangular end,...

    MODIFICATION TO ULTEGRA SYSTEM RAPID PLATELET FUNCTION ASSAY - TRAP (RPFA-TRAP)

    FDA 510(k)
    FDA Class 2 ·Hematology

    SMITH & NEPHEW RESTIM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    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