BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    HOWMEDICA V40 22MM FEMORAL HEAD

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OMNIGUIDE BEAMPATH CO2 MARK I LASER BEAM DELIVERY

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Self-Forming Magnet (Flexagon Plus OTOLoc)

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

    BONE SCR SELF-TAP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 30, 2020

    FIRSTPASS SUTURE PASSER

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORPORATION·Product code GCJ·February 5, 2013

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 6, 2011

    MILLENNIUM M10 OXYGEN CONCENTRATOR

    FDA Adverse Event
    Injury ·RESPIRONICS, INC.·Product code CAW·July 10, 2014

    CERAMIC ELECTRODE TIP L-HK F/GK372R

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code GEI·July 5, 2019