BEUDAMED
    10 results · 21ms · 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 ×

    C-VBR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    K152468

    FDA UDI
    Shenzhen Vistar Medical Supplies Co.,Ltd.·96973521874184·Reusable NIBP cuff,Thigh,single tube, HP connector

    CSF DRAINAGE SYSTEM USED WITH POLE MOUNT SYSTEM

    FDA Adverse Event
    Injury ·INTEGRA NEUROSCIENCES PR·Product code JXG·March 8, 2017

    URIC ACID MODEL 3P39

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    ESTEEM STRETCHY VINYL GLOVE WITH COATING

    FDA 510(k)
    FDA Class 1 ·General Hospital

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 27, 2024

    INFINITY DENTAL IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·ACE SURGICAL SUPPLY CO.·Product code DZE·June 5, 2013

    AXSYM RUBELLA IGG ANTIBODY

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code LFX·September 10, 2008

    INTEGRIS H5000C/ALLURA 9C

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code IZI·June 27, 2011

    ELEKTA LIMITED Elekta Synergy, REF MRT 8501, MRT 8511; Medical Charged-Particle Radiation Therapy System Accelerator, Linear

    FDA Enforcement
    Class II ·Ongoing·Elekta, Inc.·December 13, 2023