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

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    Atlantis suprastructures

    FDA 510(k)
    FDA Class 2 ·Dental

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471130463·K-WIRE - DOUBLE TROCAR WITH GUIDE 0.6mm DIA x 1...

    AVAMAX VERTEBRAL BALLOON

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TUMARK PROFESSIONAL, MODEL 271560, MR-TUMARK PROFESSIONAL, MODEL 601560

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

    BD NEXIVA¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·August 12, 2022

    BD NEXIVA DUAL PORT WITH Q-SYTE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·August 24, 2022

    FLO-GARD 6201 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FRN·October 13, 2008

    PROVISIONAL LINER LOCKING SCREW

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code LXH·July 22, 2011

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·June 27, 2013