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

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    Biomet Tibial trays

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BMT GB KNEE STM 12X40

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code OIY·June 1, 2022

    ACCESS THYROGLOBULIN ANITBODY

    FDA 510(k)
    FDA Class 2 ·Immunology

    GEM-TONE BODY TRAINING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW)

    FDA Adverse Event
    Malfunction ·ANGIOSCORE, INC·Product code LIT·November 18, 2015

    SUMMIT POR TAPER SZ7 HI OFF

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code MRA·June 3, 2013

    PLUM A+ DRIVER NEW 8

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·September 12, 2014

    SCULPTRA

    FDA Adverse Event
    Injury ·SANOFIAVENTIS U.S. LLC·Product code LMH·June 23, 2011

    ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW)

    FDA Adverse Event
    Injury ·ANGIOSCORE, INC·Product code LIT·March 29, 2016

    ANGIOSCULPT PTA SCORING BALLOON CATHETER (OTW)

    FDA Adverse Event
    Malfunction ·ANGIOSCORE, INC·Product code LIT·November 26, 2015