BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    QUICKIE & ZIPPIE SERIES

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    CS 8100 CS 8100 ACCESS

    FDA 510(k)
    FDA Class 2 ·Dental

    VOYAGER LINUX

    FDA 510(k)
    FDA Class 2 ·Neurology

    INSPIRA TEXTURED SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·November 18, 2021

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE·Product code KDJ·May 22, 2013

    K-WIRE, COCR, RECON T2 RECON Ø3.2X400 MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·September 27, 2014

    CAPSURE SENSE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 14, 2011

    3.0 mm Reaming Rod/950 mm w/straight Ball Tip, Sterile

    FDA Enforcement
    Class II ·Terminated·Synthes (USA) Products LLC·November 30, 2016