BEUDAMED
    6 results · 20ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    SCIMED ULTROX TRUE MEMBRANE OXY. ULTROX I & II

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SAF FIXATIVE

    FDA 510(k)
    FDA Class 1 ·Pathology

    SYNMESH System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INOMAX DS (DELIVERY SYSTEM)

    FDA Adverse Event
    Malfunction ·INO THERAPEUTICS LLC/IKARIA·Product code MRN·October 15, 2010

    MARYLAND GSP.FORCEPS FEN.5/310MM HF CON.

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code GEI·February 19, 2014

    OBTRYX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·December 21, 2012