BEUDAMED
    9 results · 35ms · Sources: EU EUDAMED, US FDA

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    TRACH T ADAPTER

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    discovery®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011790157000·discovery® Bracket with hook, - 2° Torque, + 9°...

    Diana ChemoClave Transfer Set

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ISOLYSER HOME SHARPS MANAGEMENT (HSM), MODEL 800M; ISOLY SHARPS MANAGEMENT SYSTEM (SMS), MODELS 2400M, 4000M, 10000M, 5.

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MENTOR SMOOTH ROUND MODERATE PLUS PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·August 18, 2020

    UNKNOWN DEPUY FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·May 5, 2014

    EXTERNAL PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MILACA INC.·Product code DTE·October 15, 2012

    SCORPIO PS TIB INSERT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JWH·August 3, 2010

    5.5 HEALIX ADVANCE PEEK W/OC&ND

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code HWC·October 15, 2018