BEUDAMED
    7 results · 18ms · 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.

    ION TRAP DETECTOR (ITD)

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    OREAI-Q-TU TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    XD880A Ultrasonic Osteotomy Surgical System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COBAS C 513 ANALYZER

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·November 25, 2025

    M2A-MAGNUM MOD HD SZ 50MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·June 13, 2014

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS INNOVATION CENTER-SILICON VALLEY·Product code GEX·October 12, 2010

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·December 11, 2012