BEUDAMED
    6 results · 25ms · Sources: EU EUDAMED, US FDA

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    INTERPLAK HOME PLAQUE REMOVAL INSTRUMENT

    FDA 510(k)
    FDA Class 1 ·Dental

    SOLSTAR BRILLENMODE SPECTACLE FRAMES

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    ZEISS MULTIYAG LASER

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

    PWRD ECH FLEX 60MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·January 30, 2013

    ISYMM ASPHERIC INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·HOYA SURGICAL OPTICS INC.·Product code HQL·December 8, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·February 3, 2014