BEUDAMED
    11 results · 23ms · Sources: EU EUDAMED, US FDA

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    MEDILAS H LASER FIBERS

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

    ArgenZ ST 98x14 ML OM1

    FDA UDI
    ARGEN CORPORATION, THE·D818123385·Dental porcelain/ceramic restoration kit

    VECTOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SECURVIEW DX DIAGNOSTIC WORKSTATION

    FDA 510(k)
    FDA Class 2 ·Radiology

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 21, 2013

    SELECT SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code NVN·June 14, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 20, 2008

    EQUINOXE REVERSE SHOULDER COMPONENTS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·April 12, 2023

    EVOLUT PRO TRANSCATHETER AORTIC VALVE

    FDA Adverse Event
    Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·May 5, 2021

    ONYX

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·July 10, 2023

    ECHELON

    FDA Adverse Event
    Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRA·July 10, 2023