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

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    CATHETER INTRODUCER MODIFICATION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODEL 3500 MR-COMPATIBLE PULSE OXIMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KC 100 M

    FDA 510(k)
    FDA Class 2 ·Radiology

    TPRLC 133 T1 PPS HO 12X144MM

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LZO·December 26, 2024

    EON MINI

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL NEUROMODULATION·Product code LGW·January 7, 2013

    ANGIOSCULPT PTA SCORING BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·ANGIOSCORE, INC.·Product code LIT·December 3, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 15, 2014