BEUDAMED
    10 results · 20ms · 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.
    Filters Regulation: Us FDA ×

    INFUSION PUMP, MODEL NO. UDP-5

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

    n/a

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00613994869784·DISTRACTOR 2942023 WEDGE DISTRACTOR 14MM

    NA

    FDA UDI
    Zimmer, Inc.·00889024144125·

    LUNA INTERBODY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FUJI COMPUTED RADIOGRAPHY (FCR) CLEARVIEW CS IMAGE READER

    FDA 510(k)
    FDA Class 2 ·Radiology

    ARROW SPINAL ANESTHESIA KIT: 25 GA X 9 CM

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL LLC·Product code BSP·December 4, 2023

    IMPELLA 5.5

    FDA Adverse Event
    Death ·ABIOMED, INC.·Product code OZD·September 6, 2025

    PULSE GEN MODEL 102R

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·February 4, 2013

    ACCU-CHEK ® COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·December 30, 2010

    9800

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