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

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    ECTRA II LIGAMENT RELEASE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CHURCHILL-HS SUSPENDED VENTED IV SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CENTAURI YAG LASER SYST, EAR, NOSE , THROAT

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

    BD BACTEC PEDS PLUS/ F CULTURE VIALS

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code MDB·July 14, 2021

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A. (SMO)·Product code LWS·February 11, 2013

    840 VENTILATOR

    FDA Adverse Event
    Injury ·COVIDIEN·Product code CBK·July 11, 2014

    MULTIPLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·January 10, 2011