BEUDAMED
    8 results · 23ms · 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 ×

    SDB CERCLAGE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CAPSTONE PTC™ Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169187368·SPACER 3992616 26MM X 16MM

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198864·AK3 Ultra Insert Trial Size 6, 16mm

    CanGaroo Envelope (small), CanGaroo Envelope (medium), CanGaroo Envelope (large), CanGaroo Envelope (extra large), CanGaroo Envelope (extra extra large) (SubQ)

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

    ASCENT BOND UNIVERSAL ADHESIVE SYSTEM, MODELS 006-00029, 006-00030, 006-00044, 006-00045

    FDA 510(k)
    FDA Class 2 ·Dental

    *

    FDA Adverse Event
    FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·February 11, 2013

    INSYNC II MARQUIS

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code NIK·February 15, 2011

    CAPSURE Z

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·August 8, 2014