BEUDAMED
    9 results · 27ms · Sources: EU EUDAMED, US FDA

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    SIEMENS SC 9000 ETCO2 MODULE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    LEVEL ONE

    FDA UDI
    KLS-Martin L.P.·00888118118455·CLAMP, REDUCTION, W/O RTCH

    ENDOTRACHEAL TUBE GUIDE OR INTUBATION STYLETTE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CENTAURI YAG LASER SYST, GYNECOLOGY

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

    BD BBL¿ MGIT¿ OADC ENRICHMENT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code MDB·May 13, 2024

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LWS·February 11, 2013

    SMART MONITOR 2

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code FLS·October 14, 2010

    E360 VENTILATOR

    FDA Adverse Event
    Injury ·NEWPORT MEDICAL INSTRUMENTS, INC.·Product code CBK·July 11, 2014

    M-VIZION FEMORAL REVISION SYSTEM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code LZO·October 4, 2024