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

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    Filters Regulation: Us FDA ×

    MOBILETT Impact

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD BBL™ Sensi-Disc™ Ethionamide - 25 µg

    FDA UDI
    BECTON, DICKINSON AND COMPANY·00382902315773·Disc Ethionamide Ea-25 1 Ea

    Dornier MedTech

    FDA UDI
    DORNIER MEDTECH AMERICA, INC.·00810116022564·400 micron core/730 micron OD SMA Diode Laser F...

    LINICAL PROTEIN 2 CALIBRATION VERIFIERS LEVELS A-E FOR BECKMAN COULTER ARRAY PROTEIN SYSTEMS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    MatriDerm

    FDA 510(k)
    FDA Unclassified ·Unknown

    BD BBL¿ MGIT¿ MYCOBACTERIA GROWTH INDICATOR TUBES, 7ML

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MDB·March 8, 2023

    LENTULO PASTE CARRIER

    FDA Adverse Event
    Malfunction ·DENTSPLY MAILLEFER·Product code DZA·October 18, 2014

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTORNIC MINIMED·Product code MDS·July 22, 2011

    EON MINI

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·July 12, 2013

    Revogene, Catalog no. 610210. IVD test instrument

    FDA Enforcement
    Class II ·Ongoing·Meridian Bioscience Inc·August 3, 2022