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

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    Dental Implant OKTAGON Bone Level

    FDA 510(k)
    FDA Class 2 ·Dental

    BD PEN NEEDLE¿ ULTRA-FINE III

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·May 15, 2019

    BD PEN NEEDLE¿ ULTRA-FINE III

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·May 3, 2019

    DEMETECH STERILE SYNTHETIC ABSORBABLE SUTURES (PGA) AND NEEDLES

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

    QUANTA SYSTEM DUOLITE

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

    BD PEN NEEDLE¿ ULTRA-FINE III

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code NSC·July 3, 2019

    PFC*SIGMA/OV/DOME PAT 3PEG,41

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON MEDICAL (SUZHOU) LTD. 3006356043·Product code JWH·October 6, 2014

    IVT DISPOSABLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CALI·Product code KPE·June 3, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·June 2, 2011

    BD PEN NEEDLE¿ ULTRA-FINE III

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·January 14, 2019