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

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    PLUSTRON ION TOOTHBRUSH SYSTEM

    FDA 510(k)
    FDA Class 1 ·Dental

    KMEDIC

    FDA UDI
    TELEFLEX INCORPORATED·24026704293746·

    QWIX POSITIONING SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Trojan Supra Lubricated Polyurethane Male Condom

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

    BONE ANCHOR SYSTEM FOR SOFT TISSUE SUPPORT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SPENCER·Product code MBI·April 27, 2012

    TPRLC 133 MP TYPE1 PPS HO 13.0

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KWA·September 27, 2021

    NSE FOOTSWITCH

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code ERL·February 21, 2013

    MEDISENSE OPTIUM

    FDA Adverse Event
    Malfunction ·Product code NBW·January 27, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 31, 2014

    Fixed Core Straight Safety Wire Guide, Guidewire, Global Product Number G14285

    FDA Enforcement
    Class II ·Terminated·Cook Inc.·February 12, 2020