BEUDAMED
    37 results · 28ms · Sources: EU EUDAMED, US FDA

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    Access anti-HAV IgM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Painmaster MCT Patch

    FDA 510(k)
    FDA Class 2 ·Neurology

    PROFEMUR RENAISSANCE HIP STEM

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    CSF-CARDIAC/PERITONEAL CATHETER, STANDARD, 90CM

    FDA Adverse Event
    Injury ·MEDTRONIC PS MEDICAL·Product code JXG·January 16, 1998

    STERNGOLD IMPLAMED, FIXTURE, TI,

    FDA Adverse Event
    Injury ·STERNGOLD IMPLAMED·Product code DZE·February 16, 1998

    MEDSTONE STS LITHOTRIPTER

    FDA Adverse Event
    Injury ·MEDSTONE INTERNATIONAL, INC.·Product code LNS·June 15, 1998

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code NRA·July 20, 2015

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code NRA·July 20, 2015

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code NRA·July 20, 2015

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code NRA·July 20, 2015

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code NRA·July 20, 2015

    UNKNOWN OXFORD KNEE

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code NRA·July 20, 2015

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code NRA·July 20, 2015

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code NRA·July 20, 2015

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code NRA·July 20, 2015

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code NRA·July 20, 2015

    TITANIUM SOLID TIBIAL NAIL

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HSB·July 24, 1998

    UNKNOWN KNEE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code NRA·July 20, 2015

    MEDTRONIC

    FDA Adverse Event
    Malfunction ·MEDTRONIC INC·Product code DXY·July 29, 1998

    SYNCHROMED

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code LKK·September 3, 1999