BEUDAMED
    9 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    DLP Vein Graft Cannula

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    3D Printed Interbody Systems

    FDA UDI
    Seaspine Orthopedics Corporation·10889981280864·No Profile Spacer, 14x13x10mm, 7 Degree, 3D

    EMERGE MEDICAL DISTAL RADIUS SET

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MSA HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PELVICOL (BARD) 8CM X 12CM

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY TISSUE·Product code FTL·May 24, 2013

    SWIFT-LOCK ANCHOR

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·June 23, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·September 3, 2008

    ARCHITECT C8000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·January 13, 2020

    1 Step 12 Panel Cup, Item No. NBCA-12M-W

    FDA Enforcement
    Class III ·Terminated·Ameditech Inc·December 30, 2015