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

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    GuideLiner V3 Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Ophthalmic Ring

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100813·FLIERINGA FIXATION RING 20MM

    SPINESMITH CYNCH SPINAL SYSTEM - VISUALIF INTERBODY FUSION IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SIEMENS DIAGNOSTIC ULTRASOUND SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Radiology

    AQUILEX FLUID CONTROL SYSTEM

    FDA Adverse Event
    Malfunction ·W.O.M. WORLD OF MEDICINE GMBH·Product code HIG·March 12, 2020

    Widex

    FDA UDI
    Widex A/S·05706069819458·Widex UNIQUE U-FS (Metallic Blue ) 30, Telecoil...

    Widex

    FDA UDI
    Widex A/S·05706069792751·Widex UNIQUE U-PA (Metallic Blue ) 30, RC coil

    PLM A+ SPANISH 110V

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·June 11, 2013

    DATALINK/DL2000 DATA MANAGER, COMMAND CENTRAL

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JQP·June 15, 2011

    SYNERGY XVI

    FDA Adverse Event
    Injury ·ELEKTA LTD.·Product code IYE·September 23, 2008