BEUDAMED
    35 results · 31ms · Sources: EU EUDAMED, US FDA

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    ERBE ESU MODEL VIO DV WITH ACCESSORIES

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

    NA

    FDA UDI
    MEDTRONIC XOMED, INC.·00681490034548·PROSTHESIS 1133180 CUP STAPES .4X4.0 SST

    Oticon

    FDA UDI
    Oticon A/S·05707131259691·RIA, MINIBTE 312 WL 85 TC

    FALCON SPACER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CLEANSER ROOT CANAL

    FDA 510(k)
    FDA Unclassified ·Unknown

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·January 8, 2026

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·August 14, 2025

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·December 4, 2025

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·December 4, 2025

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·November 5, 2025

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·March 25, 2026

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·November 21, 2024

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·March 6, 2025

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·October 29, 2025

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·August 6, 2025

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·May 1, 2026

    EXPRESS LD ILIAC / BILIARY

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIO·November 21, 2024

    PEEK ZIP SUTURE ANCHOR, 5.5MM

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code MBI·May 29, 2013

    PROGRAMMING SOFTWARE

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·August 22, 2008

    ROTABLATOR ROTATIONAL ATHERECTOMY SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - COSTA RICA·Product code MCX·June 20, 2011