BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    LABEL, STERILIZATION INDICATOR; DUAL STEAM/E.O.GAS

    FDA 510(k)
    FDA Class 2 ·General Hospital

    MAXI-VAC TM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    RESTORIS MULTICOMPARTMENTAL KNEE (MCK) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    STEAM STER LOCKS ORANGE

    FDA Adverse Event
    Injury ·AESCULAP INC·Product code KCT·October 12, 2016

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·June 11, 2014

    NEW LIGASURE 5MM

    FDA Adverse Event
    Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·November 1, 2010

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·December 31, 2012

    STEAM STER LOCKS ORANGE

    FDA Adverse Event
    Malfunction ·AESCULAP INC·Product code KCT·July 26, 2016