BEUDAMED
    11 results · 21ms · Sources: EU EUDAMED, US FDA

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    WALLSTENT ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code JCT·January 15, 2025

    WALLSTENT TRACHEOBRONCHIAL ENDOPROSTHESIS AND WALLSTENT TRACHEOBRONCHIAL ENDOPROSTHESIS WITH PERMALUME COVERING

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

    WALLSTENT ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MAF·December 22, 2025

    WALLSTENT ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MAF·December 1, 2025

    DeltaForm HD

    FDA UDI
    Merz Dental GmbH·D7091980163·DeltaForm HD lower posteriors, L, BL1 -MADE IN ...

    TransEnterix Senhance Surgical System

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

    COOLTOUCH MODELS LC215 AND COOLLIPO

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

    EMSYS LNR AOX +4N 50X36

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·January 14, 2026

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 5, 2014

    PIPELINE EMBOLIZATION DEVICE

    FDA Adverse Event
    Injury ·EV3 NEUROVASCULAR·Product code OUT·February 27, 2013

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Death ·AV-TEMECULA-CT·Product code NIQ·February 7, 2011