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

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    Filters Regulation: Us FDA ×

    WorkMate Claris System, WorkMate Claris System Display Plus

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Valencia Pedicle Screw System

    FDA UDI
    Altus Spine, LLC·B41791519111·T25 Locking Cap

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100264·KATENA DBL-X ASPIRATING SPECULUM K-WIRE

    CASTROVIEJO NEEDLE HOLDER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896017696·CASTROVIEJO NEEDLE HOLDER WITHOUT LOCK CURVED T...

    IMMUKNOW-THE CYLEX IMMUNE CELLFUNCTION ASSAY

    FDA 510(k)
    FDA Class 2 ·Hematology

    GELITA-SPON

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    VALENCIA MIS

    FDA Adverse Event
    Injury ·ALTUS SPINE·Product code KWQ·December 22, 2022

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code NAY·January 11, 2019

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code NAY·January 11, 2019

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code OLO·March 13, 2019

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·October 6, 2014

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·June 7, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 7, 2011

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code OLO·April 10, 2019

    ROSA ONE

    FDA Adverse Event
    Injury ·MEDTECH SA·Product code OLO·February 22, 2019

    ROSA ONE

    FDA Adverse Event
    Injury ·MEDTECH SA·Product code OLO·March 11, 2019

    ROSA ONE

    FDA Adverse Event
    Malfunction ·MEDTECH SA·Product code NAY·April 3, 2019