BEUDAMED
    8 results · 20ms · 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 ×

    Fractional CO2 Laser Therapy System (FG900-S); Fractional CO2 Laser Therapy System (FG900-S2)

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

    TITAN OTR NAR SCRO 16CM

    FDA Adverse Event
    Injury ·COLOPLAST A/S·Product code FHW·February 12, 2018

    ACUVUE (ETAFILCON A) SOFT CONTACT LENS FOR PRESBYOPIA

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    BIS PEDIATRIC SENSOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    TARGETING ARM PROX. LAT TIBIA LEFT

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS SELZACH·Product code LXH·February 2, 2012

    COBAS 6000 C501 MODULE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code CEM·November 19, 2008

    MP50 INTELLIVUE PATIENT MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·September 2, 2011

    OBTRYX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·July 22, 2013