BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    STACLOT HEPARIN TEST KIT

    FDA 510(k)
    FDA Class 2 ·Hematology

    TRANSMITTER, ZS-940PA SERIES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Voyant Open Sealer-Divider Device

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

    UNK CAPIOX ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTM·April 8, 2019

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code DRM·January 9, 2013

    ACRYSOF IQ TORIC

    FDA Adverse Event
    Other ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·December 2, 2010

    R3 PRIMARY 46MM ID US COCR LNR 58MM

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDH·July 18, 2014

    CAPIOX ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTM·October 10, 2018

    ARTERIAL FILTER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DTM·June 28, 2019