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

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    Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517568274·CoRoent Ant TLIF PEEK, 9x13x34mm 8°

    DIGIVIEW 250

    FDA 510(k)
    FDA Class 2 ·Radiology

    3.0T 16 CHANNEL HEAD NECK SPINE COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    T:SLIM G5 SYSTEM

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code OYC·July 17, 2019

    BD VACUTAINER® SERUM BLOOD COLLECTION TUBES

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·March 17, 2022

    MATNEU SCR Ø1.5 SELF-DRILL L4 TAN 4U I/C

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HWC·June 27, 2013

    CONTOUR

    FDA Adverse Event
    Injury ·BAYER HEALTHCARE, LLC·Product code NBW·July 28, 2011

    EXCELON TRANSBRONCHIAL ASPIRATION NEEDLE

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code EOQ·October 7, 2008