BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    reepot Nd; YAG laser system

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

    STERIL-PEEL

    FDA UDI
    AMD Medicom Inc·D830222555·STERIL-PEEL SS POUCH 12" X 15"

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111162411·MAYO DISS SCISS DEL CVD 5 1/2

    ACCOLADE C FEMORAL STEMS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    STERITEC LEAD FREE STERILIZATION PROCESS INDICATOR TAPE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE REHABILITATION EQUIP·Product code CAW·November 4, 2014

    PROXIMATE** SKIN STAPLER 35 REGULAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDT·August 25, 2011

    GYNECARE TVT OBURATOR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·July 12, 2013