BEUDAMED
    12 results · 22ms · Sources: EU EUDAMED, US FDA

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    EZER, Portable X-ray System

    FDA 510(k)
    FDA Class 2 ·Radiology

    Phasix

    FDA UDI
    Davol Inc.·00801741107665·Phasix Mesh, 14" x 14" (35 cm x 35 cm), Square

    AGXO

    FDA UDI
    Oticon A/S·05707131342690·G200, MINIRITE T 312 2.4G C093 AGXO

    AUTOLOG AUTOTRANSFUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    VACPLUS SUCTION UNIT

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

    BD PRECISIONGLIDE¿ 27 G X 1/2" HYPODERMIC NEEDLES

    FDA Adverse Event
    Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code FMI·February 1, 2023

    BD SYRINGE 10ML LL BNS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON DE MEXICO·Product code FMF·April 9, 2025

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN·Product code CBK·October 22, 2014

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·June 27, 2013

    ACCU-CHEK ® ACTIVE

    FDA Adverse Event
    Injury ·ROCHE DIAGNOSTICS·Product code NBW·August 5, 2011

    INDIGO SYSTEM ASPIRATION CATHETER 7D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code QEW·December 10, 2024

    INDIGO SYSTEM ASPIRATION CATHETER 7D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code QEW·January 5, 2023