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

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    ALPHA MICRON-40 FILTER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MICT TSH

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    SPL-50 SPIROLYSER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Malfunction ·WAVELIGHT GMBH·Product code LZS·March 21, 2014

    SYNCRA CRT-P

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code NVZ·October 31, 2012

    BECKMAN COULTER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code JJE·August 16, 2010

    Driver Instrument, part of the Superion Indirect Decompression System, REF: 102-9800, used with the Superion Indirect Decompression System IFU, Superion IDS Kit IFU, Surgical Technique Manual

    FDA Recall
    Open, Classified ·Boston Scientific Neuromodulation Corporation·Product code NQO·May 12, 2023