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

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    SAPPHIRE INFUSION PUMP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    JOYSTICK

    FDA UDI
    Aktormed GmbH·04260463843897·

    JUSHA-C31 MEDICAL DISPLAY

    FDA 510(k)
    FDA Class 2 ·Radiology

    SYNTHES CONTOURED SYNMESH SPACER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNSPECIFIED PRIMARY PLUM SET

    FDA Adverse Event
    Malfunction ·ICU MEDICAL COSTA RICA LTD.·Product code FPA·October 3, 2024

    LAMITRODE TRIPOLE 16

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL NEUROMODULATION·Product code LGW·May 24, 2013

    ALARIS PUMP MODULE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP·Product code FPA·June 15, 2011

    STERIS SYSTEM 1

    FDA Adverse Event
    Other ·STERIS CORPORATION·Product code MLR·August 20, 2008

    UNSPECIFIED PRIMARY PLUM SET CLAVE PORT, CLAVE Y-SITE, SECURE LOCK

    FDA Adverse Event
    Malfunction ·ICU MEDICAL COSTA RICA LTD.·Product code FPA·November 24, 2024

    SPINAL/EPIDURAL NEEDLES & TRAYS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code BSP·October 23, 2025

    cobas 6000 Modular Series system; Part Numbers: 1. 04745914001 cobas c 501 module; 2. 05036453001 cobas 6000 UL c 501 + Core Fix configuration; 3. 05036453692 - cobas 6000 UL + CORE CU; and 4. 05860636001 cobas 6000 c 501 (UL) V

    FDA Enforcement
    Class II ·Terminated·Roche Diagnostics Corporation·March 14, 2018