BEUDAMED
    12 results · 21ms · Sources: EU EUDAMED, US FDA

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    TRAPEZOIDAL MALAR IMPLANT

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·00636257073421·PROTECT PATELLA TRACKING BRACE, LT, LG

    Accu-Beam

    FDA UDI
    TRANSAMERICAN TECHNOLOGIES INTERNATIONAL·B1779115130·Re-usable fiberoptic handpiece for lasers 13 ga...

    "1.5MM" SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036053314·

    MP3U, POWER WHEELCHAIR

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    CX50 DIAGNOSTIC ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    BRILLIANCE 64

    FDA Adverse Event
    PHILIPS MEDICAL SYSTEMS (CLEVELAND), INC.·Product code JAK·May 27, 2014

    ENDOVIVE INITIAL PLACEMENT PEG KIT, DIRECT PEJ KIT, AND PEG SAFETY KIT

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - SPENCER·Product code KNT·December 1, 2010

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·January 11, 2013

    "1.5MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·April 2, 2019

    "1.5MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·April 10, 2019

    "1.5MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·August 3, 2018