BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    TRILOGY ACETABULAR SYSTEM LONGEVITY CROSSLINKED POLYETHYLENE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Eargo 5

    FDA UDI
    Eargo, Inc.·00850010429281·Medium Open Petals

    TRIMIRA IDENTAFI 3000

    FDA 510(k)
    FDA Class 2 ·Dental

    MONITOR, PRESSURVEIL

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·March 5, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011

    CAPSUREFIX MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MPRI·Product code NVN·August 7, 2014

    UNKNOWN

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·June 9, 2021

    ZIMMON PANCREATIC STENT

    FDA Adverse Event
    Malfunction ·COOK IRELAND LTD·Product code FGE·October 16, 2020