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

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    Filters Regulation: Us FDA ×

    MANDIBULAR BONE DISTRACTOR II

    FDA 510(k)
    FDA Class 2 ·Dental

    Tuohy NRFit

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PEPER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TITANIUM NEXGEN LCCL FEMORAL SZ C-LT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 21, 2018

    3.5MM LOCKING SCREW SLF-TPNG W/STARDRIVE RECESS 42MM

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code HWC·February 14, 2013

    NATURALYTE

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·July 15, 2014

    EASYSTAND 5000

    FDA Adverse Event
    Other ·ALTIMATE MEDICAL, INC.·Product code IKX·January 10, 2011

    NEXGEN LEGACY POSTERIOR STABILIZED ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·June 16, 2016

    EVOLUT FX DCS

    FDA Adverse Event
    Malfunction ·MEDTRONIC IRELAND·Product code NPT·October 16, 2025