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

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    Filters Regulation: Us FDA ×

    TearCare MGX System

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Sasmar Vanilla

    FDA UDI
    Sasmar Pharmaceuticals SPRL·09337213008266·PERSONAL LUBRICANT

    Symmetry Surgical

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482001585·Symmetry® Curette, Spinal, Straight, Size 1, 11...

    SOLAR GI SYSTEM

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

    SASMAR ORIGINAL, SASMAR CLASSIC

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    UNKNOWN PRODUCT - SET SCREW

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HWC·October 12, 2012

    SOLETRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·February 12, 2014

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·February 12, 2014

    UNK -- IOL

    FDA Adverse Event
    Malfunction ·ALCON RESEARCH, LTD.·Product code HQL·October 30, 2008

    U-P REUS H/C 5X10.5 BULK 12/CA

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code IMD·July 20, 2011

    DELTAPLUSH - PLATINUM MICROCOIL

    FDA Adverse Event
    Injury ·MICRUS ENDOVASCULAR, LLC·Product code HCG·July 17, 2013