BEUDAMED
    14 results · 20ms · Sources: EU EUDAMED, US FDA

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    POCKET SIZE FETAL HEART DETECTOR

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

    Grasping forceps

    FDA UDI
    SOPRO-COMEG GmbH·04059082022406·

    HUMAN KAPPA AND LAMBDA FREE KITFOR USE ON THE SPA PLUS ANALYSER

    FDA 510(k)
    FDA Class 2 ·Immunology

    DUET SUTURE ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Titan™

    FDA UDI
    Ascension Orthopedics, Inc.·10381780244585·Titan™ Total Shoulder System The solid center s...

    FEMORAL STEM 12/14 NECK TAPER STANDARD OFFSET SIZE 1 130 MM STEM LENGTH

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code JDI·March 12, 2019

    FEMORAL HEAD STERILE PRODUCT DO NOT RESTERILIZE 12/14 TAPER

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code LPH·March 12, 2019

    FEMORAL STEM 12/14 NECK TAPER STANDARD OFFSET

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code JDI·October 3, 2018

    FEMORAL HEAD

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code LPH·October 3, 2018

    ROTALINK¿ PLUS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - CORK·Product code MCX·January 17, 2013

    SHILEY FENESTRATED LOW PRESSURE CUFFED

    FDA Adverse Event
    Injury ·COVIDIEN/FORMERLY TYCO HEALTHCARE·Product code JOH·December 2, 2010

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 8, 2014

    DURAL ALPHA INSERT W RIM II/32

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LPH·March 12, 2019

    DURASUL, ALPHA INSERT, HOODED, II/32

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LPH·September 28, 2018