BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    ROADRUNNER RLTF GUIDE WIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110966·STERILIZING CASE 4-KNIVES

    SPEEDBAND SUPERVIEW SUPER 7, INJECTION SPEEDBAND SUPERVIEW SUPER 7, MODELS 4205 AND 4238

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    3.9MM REELX STT SUTURE ANCHOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COMBISET WITH BVM

    FDA Adverse Event
    Malfunction ·REYNOSA MANUFACTURING·Product code FJK·November 15, 2010

    PROGRASP FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 8, 2014

    CENTRA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·December 26, 2012