BEUDAMED
    10 results · 26ms · 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.

    LYFO(TM) DIFFERENTIAL DISK

    FDA 510(k)
    FDA Class 1 ·Microbiology

    PEDIATRIC VENTILATOR AND PARTNER VOLUME MONITOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DOPPLER UPGRADE FOR AUSONICS OPUS 1 REAL TIME SCAN

    FDA 510(k)
    FDA Class 1 ·Radiology

    HF-RESECTION ELECTRODE, LOOP, 24 FR., 0.35 WIRE, 12, STERILE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·August 11, 2021

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·February 6, 2013

    ARTICUL/EZE BALL 28 +1.5 GR

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON MEDICAL (DEPUY-SUZHOU) LTD.·Product code JDI·December 30, 2010

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·July 21, 2014

    HF-RESECTION ELECTRODE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·March 8, 2023

    HF-RESECTION ELECTRODE

    FDA Adverse Event
    Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GCP·March 8, 2023

    UNKNOWN

    FDA Adverse Event
    Injury ·OLYMPUS WINTER & IBE GMBH·Product code KNS·October 21, 2022