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

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    ANYVIEW DR SERIES FPD Fluoroscopic Mobile C-arm ANYVIEW-240DR, ANYVIEW-320DR, ANYVIEW-500DR

    FDA 510(k)
    FDA Class 2 ·Radiology

    All Poly Monotrial UC

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215081300·

    6180473

    FDA Adverse Event
    Malfunction ·December 16, 2016

    OLYMPUS EMPOWER H65

    FDA Adverse Event
    Malfunction ·QUANTA SYSTEM S.P.A.·Product code GEX·May 19, 2022

    NANOTACK SUTURE ANCHOR 1.4MM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EMBRYOASSIST AND EMBRYOASSIST WITH PHENOL RED

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    ADVANTAGE SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 20, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 27, 2011

    OPTI-FREE REPLENISH

    FDA Adverse Event
    Injury ·ALCON - FORT WORTH/ALCON LABORATORIES, INC.·Product code LPN·September 26, 2008

    ENNOVATE POLYAX.SCREW 6.5X45MM FENESTR.

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code NKB·December 21, 2018

    ENNOVATE POLYAX.SCREW 7.5X40MM FENESTR.

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code NKB·December 21, 2018