BEUDAMED
    8 results · 100ms · 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.

    Emergency Stretcher & Stretcher Accessories

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·ZHANGJIAGANG XIEHE MEDICAL APPARATUS&INSTRUMENTS CO.,LTD.·47 devices

    BOLERO

    FDA Adverse Event
    Malfunction ·ARJO HOSPITAL EQUIPMENT AB·Product code FSA·September 25, 2006

    VENTRI

    FDA Adverse Event
    Injury ·GE MEDICAL SYSTEMS ISRAEL, FUNCTIONAL IMAGING·Product code KPS·October 25, 2011

    VIKING XL

    FDA Adverse Event
    Malfunction ·LIKO AB·Product code FSA·September 30, 2024

    GOLVO 9000

    FDA Adverse Event
    Malfunction ·LIKO AB·Product code FSA·March 15, 2022

    VIKING XL

    FDA Adverse Event
    Malfunction ·LIKO AB·Product code FSA·March 15, 2022

    MULTIRALL 200

    FDA Adverse Event
    Injury ·LIKO AB·Product code FSA·June 8, 2022

    DAVINCI X

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL, INC·Product code NAY·July 29, 2025