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

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    anti-bacterial bandage

    FDA 510(k)
    FDA Unclassified ·Unknown

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694057141·2.0mm Screw Block, ICON

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450155783·

    SCOUT (SINUS CORNARIUS UTILITY TOOL), MODEL 335 117

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ABBOTT GEMSTAR I.V. INFUSION PUMP - 7 THERAPY CONFIGURATION, 6 THERAPY CONFIGURATION, 1 THERAPY CONFIGURATION

    FDA 510(k)
    FDA Class 2 ·General Hospital

    UNK GEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·UNKNOWN MANUFACTURER·Product code FTR·November 20, 2012

    UNK SALINE IMPLANT

    FDA Adverse Event
    Injury ·UNKNOWN MANUFACTURER·Product code FWM·November 20, 2012

    UNK SALINE IMPLANT

    FDA Adverse Event
    Injury ·UNKNOWN MANUFACTURER·Product code FWM·February 7, 2014

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·October 12, 2012

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·May 1, 2012

    STARCLOSE VASCULAR CLOSURE SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR - VASCULAR SOLUTIONS·Product code MGB·April 21, 2008

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·October 24, 2014

    HEARTSTART MRX

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE - ANDOVER·Product code MKJ·June 30, 2011

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 2, 2013

    PREVENA PLUS¿ INCISION MANAGEMENT SYSTEM

    FDA Adverse Event
    Injury ·KINETIC CONCEPTS, INC.·Product code OMP·July 19, 2019

    TRANSFIX IMPLANT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MAI·August 16, 2012

    CABLE TENSIONER

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code LXH·October 8, 2014

    VICRYL PLUS POLYGLACTIN 910 SUTURE UNKNOWN PROD

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·November 20, 2017

    NEEDLE 18GA 1-1/2IN SB TW

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·December 30, 2020

    DELTA CER HEAD 12/14 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LZO·September 25, 2018