BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Reprocessed Achieve Catheter Connecting Cable

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·October 10, 2002

    STRETCH VINYL EXAMINATION GLOVE, POWDER FREE, YELLOW/WHITE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ENDO GIA SINGLEUSE DUET TRS RELOAD WITH TRI0STAPLE TECHNOLOGY

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

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 16, 2015

    WALLSTENT ENDOPROSTHESIS ENDOSCOPIC BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code FGE·October 7, 2008

    2520274-2013-03200

    FDA Adverse Event
    Injury ·SYNTHES, USA·Product code KTW·June 27, 2013

    MICRO INCISION VACUUM PACK

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB, INC.·Product code HQC·July 13, 2011