BEUDAMED
    6 results · 73ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    TRUE-SEE SYSTEMS, Inc

    FDA registration
    TRUE-SEE SYSTEMS, Inc·1 product·🇺🇸 United States

    ARTEGRAFT

    FDA Adverse Event
    Injury ·ARTEGRAFT, INC.·Product code LXA·June 30, 2017

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·March 13, 2025

    ZILVER FLEX 35 VASCULAR SELF-EXPANDING STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code NIO·July 27, 2022

    ZILVER FLEX 35 VASCULAR SELF-EXPANDING STENT

    FDA Adverse Event
    Injury ·COOK IRELAND LTD·Product code NIO·July 27, 2022

    CMC Medical Devices & Drugs SL

    Authorized representative
    🇪🇸 Spain·698 Manufacturers·11260 Devices