BEUDAMED
    57 results · 34ms · Sources: EU EUDAMED, US FDA

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    Powder Free Black Nitrile Examination Glove

    FDA 510(k)
    FDA Class 1 ·General Hospital

    RNAscope™ ISH Probe Kappa

    FDA UDI
    Advanced Cell Diagnostics, Inc.·00850042722015·RNAscope™ ISH Probe Kappa is designed to hybrid...

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180168701·TURNER WARWICK NEEDLE HOLDER, 9"

    ABSORBENT PAPER POINTS

    FDA UDI
    DiaDent Group International·08806383511650·"An absorbent paper points is an endodontic pap...

    SYMPHONY

    FDA Adverse Event
    Malfunction ·SORIN CRM·Product code NVZ·May 15, 2014

    CLINITEK ATLAS PRO 12 REAGENT PAK SYSTEM

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    OPTIMUM WETTING AND REWETTING DROP

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    OMNIPOD

    FDA Adverse Event
    Injury ·INSULET·Product code LZG·July 1, 2016

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 12, 2024

    ENDURANT

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·February 26, 2014

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·March 16, 2015

    EVOLUTION BILIARY CONTROLLED-RELEASE STENT - UNCOVERED

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code FGE·September 26, 2014

    PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code NEW·July 2, 2018

    PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAW·July 2, 2018

    EX-PRESS MINI GLAUCOMA SHUNT

    FDA Adverse Event
    Injury ·OPTONOL, LTD·Product code KYF·March 5, 2014

    EX-PRESS MINI GLAUCOMA SHUNT

    FDA Adverse Event
    Injury ·OPTONOL, LTD·Product code KYF·March 5, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 27, 2014

    ACUVUE BRAND CONTACT LENSES

    FDA Adverse Event
    Injury ·VISTAKON·Product code LPL·June 28, 2013

    HEMOPRO2 EXTENSION CABLE

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·August 3, 2011

    EX-PRESS MINI GLAUCOMA SHUNT

    FDA Adverse Event
    Injury ·OPTONOL, LTD·Product code KYF·March 5, 2014