BEUDAMED
    8 results · 19ms · Sources: EU EUDAMED, US FDA

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    COMPRESSOR/NEBULIZER #3650

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DEVILBISS

    FDA Adverse Event
    Injury ·SUNRISE MEDICAL HHG, INC.·Product code CAF·November 8, 2001

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970289·anteriors; shade C1; mould UIS

    PB-4 REPLAY UNIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ACQUASEAL BENZ

    FDA 510(k)
    FDA Class 2 ·Dental

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·April 29, 2014

    BRYAN CERVICAL DISC

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code MJO·February 20, 2013

    LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (SMALL)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·January 14, 2011