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

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    MAX-I-PROBE ENDODONTIC SEALER DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    Dentium Ti-Base

    FDA 510(k)
    FDA Class 2 ·Dental

    ARTHREX FIBERWIRE

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

    LIGACLIP ENDOSCOPIC MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Injury ·EES-ALBUQUERQUE·Product code GDO·March 14, 1997

    APEX¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - GALWAY·Product code LOX·February 21, 2013

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·January 25, 2011

    ACCU-CHEK ® SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LZG·July 31, 2014