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

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    VENTILATOR, CONTINUOUS (RESPIRATOR), MODEL LTV 1000

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    IMPROVED ENLIGHT LV

    FDA 510(k)
    FDA Class 2 ·Dental

    PERFADEX SOLUTION FOR ORGAN PRESERVATION

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

    ULTRACISION SURG DEV, CURVED SHEARS, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

    NA

    FDA UDI
    Zimmer, Inc.·00889024064997·

    NA

    FDA UDI
    Zimmer, Inc.·00889024064980·

    NA

    FDA UDI
    Zimmer, Inc.·00889024064966·

    NA

    FDA UDI
    Zimmer, Inc.·00889024064973·

    NA

    FDA UDI
    Zimmer, Inc.·00889024064959·

    ULTRACISION SURG DEV, CURVED SHEARS, ENDO

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

    ULTRACISION SURG DEV, CURVED SHEARS, ENDO

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code LFL·June 2, 2006

    ULTRACISION SURG DEV, CURVED SHEARS, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GEI·June 19, 2006

    ULTRACISION SURG DEV, CURVED SHEARS, ENDO

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 19, 2006

    ULTRACISION SURG DEV, CURVED SHEARS, ENDO

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 19, 2006

    ULTRACISION SURG DEV, CURVED SHEARS, ENDO

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GEI·June 19, 2006

    ULTRACISION SURG DEV, CURVED SHEARS, OPEN

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

    ULTRACISION SURG DEV, CURVED SHEARS, ENDO

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GEI·June 19, 2006

    ATTAIN ABILITY PLUS

    FDA Adverse Event
    Death ·MPRI·Product code OJX·March 13, 2013

    ASR UNI FEMORAL IMPL SIZE 43

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 16, 2011

    IMPLANTIUM

    FDA Adverse Event
    Other ·DENTIUM CO., LTD.·Product code DZE·February 22, 2008