BEUDAMED
    12 results · 19ms · Sources: EU EUDAMED, US FDA

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    K-KLOSURE 2 INCH LENGTH/4 INCH LENGTH/8 INCH LENGTH/12 INCH LENGTH

    FDA 510(k)
    FDA Class 1 ·General Hospital

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970441·anteriors; shade D4; mould BS

    SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295250494·SIGMA TIBIAL INSERT FIXED BEARING CURVED PLUS 2...

    METASURG SUBTALAR IMPLANT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ElectroTek

    FDA 510(k)
    FDA Class 2 ·Neurology

    FISHER & PAYKEL HEALTHCARE

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code FMT·April 30, 2026

    FISHER & PAYKEL HEALTHCARE

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code FMT·December 3, 2025

    FISHER & PAYKEL HEALTHCARE

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code FMT·October 16, 2025

    TENDRIL ST

    FDA Adverse Event
    Death ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·February 20, 2013

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·January 18, 2011

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·July 31, 2014

    CERAMIC ELECTRODE TIP L-HK F/GK372R

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