BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    SILHOUETTE, MODEL 1000.01

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    MaXcess

    FDA UDI
    Nuvasive, Inc.·00887517128027·MAS PLIF Drill, 5.0mm Extended

    Up&Up

    FDA UDI
    TARGET CORPORATION·00014007483001·Supportive Elastic Athletic Wrap - 3" - Up&Up

    VIP- VARIABLE INTENSITY POLYMERIZER

    FDA 510(k)
    FDA Class 2 ·Dental

    PROPORT PLASTIC VENOUS IMPLANTABLE ACCESS SYSTEMS PRE-ASSEMBLED WITH SILICONE CATHETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    PRECISION NOVI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 15, 2023

    GPSIII 30ML PLATELET CONCENTRATION KIT WITH ACD-A

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KSS·August 22, 2018

    EXOSEAL VASCULAR CLOSURE DEVICE (VCD)

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code MGB·April 22, 2013

    STRETCHER

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·March 29, 2011

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code MUZ·July 3, 2008