BEUDAMED
    10 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Garment Electrodes

    FDA 510(k)
    FDA Class 2 ·Neurology

    Surgical Face Mask

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

    HTS COIL

    FDA 510(k)
    FDA Class 2 ·Radiology

    SOLAR 8000I

    FDA Adverse Event
    Malfunction ·GE HEALTHCARE·Product code DRT·November 6, 2008

    SEPRAFILM (SODIUM HYALURONATE, CARBOXYMETHYLCELLULOSE) MEMBRANE

    FDA Adverse Event
    Other ·GENZYME BIOSURGERY (SEPRAFILM/PACK)·Product code MCN·August 10, 2011

    TOMOFIX TIB-HEAD-PL MED PROX 4HO TI

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code KTT·July 12, 2013

    2.4MM TI VA LOCKING SCREW STARDRIVE 20MM-STERILE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·December 12, 2018

    BD KIESTRA IDENTIFA

    FDA Adverse Event
    Malfunction ·BD KIESTRA LAB AUTOMATION·Product code QBN·October 8, 2025

    BD KIESTRA¿ IDENTIFA

    FDA Adverse Event
    Malfunction ·BD KIESTRA LAB AUTOMATION·Product code QBN·December 9, 2024

    2.4MM TI VA LOCKING SCREW STARDRIVE 20MM-STERILE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·December 12, 2018