BEUDAMED
    11 results · 27ms · 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 ×

    G.E. STERILE AMNIOCENTESIS TRAY

    FDA 510(k)
    FDA Class 1 ·Obstetrics/Gynecology

    Peerless Buccal Tube

    FDA UDI
    ORMCO CORPORATION·00889989023022·PRLS 10 UFM COMBI B/T -10TRQ 22X51 RT

    iNSitu™ Hip System

    FDA UDI
    NEXTSTEP ARTHROPEDIX, LLC·00816127023866·Hohmann Angled Retractor

    MODIFICATION TO CD HORIZON SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ADAMANT ZIRCONIA DISC

    FDA 510(k)
    FDA Class 2 ·Dental

    11MM/130 DEG TI CANN TFNA 170MM - STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code HSB·July 28, 2016

    TFNA HELICAL BLADE 90MM STERILE

    FDA Adverse Event
    Injury ·SYNTHES ELMIRA·Product code HSB·June 16, 2016

    HOURGLASS

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code MQP·June 16, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 14, 2013

    SYNVISC ONE (HYLAN G-F 20) INJECTION

    FDA Adverse Event
    Other ·GENZYME BIOSURGERY (RIDGEFIELD)·Product code MOZ·January 3, 2011

    EON

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION·Product code GZB·July 23, 2014