BEUDAMED
    7 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 ×

    IMAGE FUSION AND REVIEW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    ORTHOGLIDE LATERAL KNEE IMPLANT AND INSTRUMENTS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ReliefBand 1.5

    FDA 510(k)
    FDA Class 2 ·Neurology

    MENTOR SMOOTH ROUND MODERATE PLUS PROFILE

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FWM·March 14, 2019

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Death ·INVACARE FLORIDA OPERATIONS·Product code CAW·February 21, 2013

    UNICEL® DXC 600 PRO SYNCHRON® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·Product code JJE·January 28, 2011

    KIMVENT MIRCROCUFF SUBGLOTTIC SUCTIONING ENDOTRACHEAL TUBES

    FDA Adverse Event
    Malfunction ·KIMBERLY CLARK CORPORATION·Product code BTR·July 9, 2014