BEUDAMED
    7 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.

    HERPES GROUP IGG ELISA TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Microbiology

    FREQUENCER, MODEL 1001

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    DERMABOND PRINEO Skin Closure System

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

    IMPELLA CP

    FDA Adverse Event
    Injury ·ABIOMED, INC.·Product code OZD·September 24, 2025

    C-QUR EDGE MESH

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORP.·Product code FTL·January 2, 2013

    IAB: 8FR - 40 CC FOS

    FDA Adverse Event
    Malfunction ·ARROW INTL., INC.·Product code DSP·December 21, 2010

    36MM COCR MOD HD STD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·July 29, 2014