BEUDAMED
    61 results · 32ms · Sources: EU EUDAMED, US FDA

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    PERICAM PSI

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ArgenPMMA 98x20-C4

    FDA UDI
    ARGEN CORPORATION, THE·D818120884·Crown And Bridge, Temporary, Resin

    NOVO Health Services, LLC

    FDA UDI
    NOVO HEALTH SERVICES, LLC·00812564031563·Basin Set

    Mini Unicycle™

    FDA UDI
    Ortho Organizers, Inc.·00190707056858·Mini Unicycle™ .120” Ligature Ties - Periwinkle

    EXCELLITE LIGHT CURE UNIT

    FDA 510(k)
    FDA Class 2 ·Dental

    STRYKER KNIFELIGHT

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

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·May 20, 2013

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·June 11, 2011

    OBTAPE TRANSOBTURATOR

    FDA Adverse Event
    Injury ·MENTOR·Product code FTL·August 15, 2008

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORP.·Product code OKS·August 19, 2014

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·January 13, 2017

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·January 5, 2017

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016