BEUDAMED
    38 results · 19ms · Sources: EU EUDAMED, US FDA

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    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515065918·Roch Ochs Hemo Fcps, str, 1x2 tth, 10"

    MSI Precision Specialty Instruments

    FDA UDI
    Med Saver, Inc.·00194613097615·Hartmann Infant Speculum, Oval 2.5mm x 3.5mm Di...

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515018778·Roch Ochs Hemo Fcps, str, 1x2 tth, 10"

    UniTip High Resolution Catheter

    FDA UDI
    Unisensor AG·07640172973578·

    INVIROSTRIPE LUER LOCK SYRINGES (1, 3, 10, 20, 30 AND 60 ML)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SHEAUMANN PL-1064

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BODY CLOCK STIMPLUS AND STIMPLUS PRO

    FDA 510(k)
    FDA Class 2 ·Neurology

    ROSA ONE

    FDA Adverse Event
    Injury ·MEDTECH SA·Product code HAW·November 10, 2017

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·April 11, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·March 15, 2018

    ROSA ONE

    FDA Adverse Event
    Injury ·MEDTECH SA·Product code HAW·June 15, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·November 10, 2017

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·March 21, 2018

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·November 16, 2017

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·November 9, 2017

    BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code FOZ·July 10, 2019

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code HAW·January 26, 2018

    OT VERIO IQ METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013

    SECURE ACUTE CARE BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·June 1, 2011

    X-STOP IPD SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SPINE LLC.·Product code NQO·August 27, 2008