BEUDAMED
    24 results · 29ms · Sources: EU EUDAMED, US FDA

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    EVOLVE EPS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INSTRUMENT DAMPING PORT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LIQUICHEK IMMUNOASSAY PLUS CONTROL, MODEL 360, 361, 362, 363

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    BILOX PROSTHESIS HEAD 12/14 28MM L

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LWJ·May 23, 2014

    EXCIA L PLASMAPORE UCAP 8/10 SIZE 11MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LWJ·March 6, 2014

    ISODUR PROSTHESIS HEAD 12/14 32MM L

    FDA Adverse Event
    Malfunction ·AESCULAP AG&CO KG·Product code LPH·August 7, 2014

    QUINTEX SEMICONSTRAINED SCREW 4.0X16MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LWJ·March 6, 2014

    BIOLOX PROSTHESIS HEAD 12/14 28MM S

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code LWJ·April 27, 2012

    EXCIA PLASMAPORE-UCAP 8/10 SIZE 11MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code MEH·June 21, 2013

    EXCIA CEMENTED 8/10 SIZE 12MM

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code JDI·November 5, 2012

    BIOLOX PROSTHESIS HEAD 12/14 28MM S

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code LWJ·April 14, 2014

    BIOLOX PROSTHESIS HEAD 12/14 28MM M

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code LWJ·April 27, 2012

    XIA 3 TITANIUM BLOCKER

    FDA Adverse Event
    Malfunction ·STRYKER SPINE-SWITZERLAND·Product code MNI·January 21, 2016

    BIOLOX PROSTHESIS HEAD 12/14 32MM L

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LWJ·March 6, 2014

    BIOLOX PROSTHESIS HEAD 8/10 32MM M

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code LZO·June 21, 2013

    BIOLOX PROSTHESIS HEAD 12/14 28MM S

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LWJ·March 6, 2014

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·April 26, 2013

    SITZMARKS

    FDA Adverse Event
    Injury ·KONSYL PHARMACEUTICALS, INC.·Product code FFX·April 28, 2011

    GORE PROPATEN VASCULAR GRAFT

    FDA Adverse Event
    Other ·W.L. GORE & ASSOCIATES, INC.·Product code DSY·July 23, 2008

    ISODUR PROSTHESIS HEAD 12/14 28MM M

    FDA Adverse Event
    Malfunction ·AESCULAP AG AND CO. KG·Product code LPH·January 16, 2015