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

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    PARA-PAK CLEAN VIAL

    FDA 510(k)
    FDA Class 1 ·Pathology

    NA

    FDA UDI
    aap Implantate AG·04042409097201·Direct measuring device, L 270, CS 5.8

    The Simple Locking Intramedullary (Slim) System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PENTAX ED-3490TK, VIDEO DUODENOSCOPE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·October 16, 2012

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·December 31, 2013

    CAPSURE SP NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·August 11, 2010

    PENTAX

    FDA Adverse Event
    Injury ·HOYA CORP.·Product code FDT·July 24, 2015

    Unify Quadra, Sterile EO, Model #/ Part #: CD3249-40/100036404, 100038435, CD3249-40Q/100036407, 100038436, CD3251-40/100036405, 100038095, 100038226, 100038437, 100038451, 100072563, CD3251-40Q/100036408, 100038214, 100038230, 100038407, 100038442, 100072564, CD3255-40/100038224, CD3255-40Q/100036514

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018