BEUDAMED
    6 results · 19ms · 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.
    Filters Regulation: Us FDA ×

    VALLEYLAB MODEL E252OH, FORCE GSU(TM) HANDSET

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

    BROWNE GA INDICATOR USE IN 2% ACTIV GLUTARALDEHYDE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    INTERFERENCE-CANNU-FLEX/SILK SCREWS-SCREW DR/G WIR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CAPSURE Z NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010

    SUPERCUT PLASTIC SCS 5-3/4 DEL

    FDA Adverse Event
    Malfunction ·INTEGRA YORK, PA INC·Product code GEI·January 16, 2013

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 10, 2014