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 ×

    ANTI-HAV IGM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Merit Medical®

    FDA UDI
    Merit Medical Systems, Inc.·00884450665633·

    LASEREX INTEGRE, MODEL LP2532

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    VERAVIEWEPOCS, MODEL VE

    FDA 510(k)
    FDA Class 2 ·Dental

    TRILOGY 200

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code CBK·August 19, 2020

    BD YELLOW 3L SHARPS COLLECTOR

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FMI·June 28, 2023

    ARCHITECT HE4 REAGENT KIT

    FDA Adverse Event
    Malfunction ·ABBOTT GMBH·Product code OIU·February 6, 2026

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·May 1, 2013

    UNKNOWN_RECONSTRUCTIVE_PRODUCT

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·September 16, 2014

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK INSTRUMENT MANUFACTURING·Product code KWP·May 18, 2011