BEUDAMED
    8 results · 19ms · 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 ×

    FOUNDATION FRACTURE STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EXCALIBUR ELECTROSURGICAL UNIT 60-5200-001

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

    PROTECTED NEEDLE WITH OR WITHOUT IV SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·October 11, 2023

    INTEGRATED APD SET W/CASSETTE3-PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·January 31, 2011

    M2A-MAGNUM MOD HD SZ 48MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·August 1, 2014

    MILLINNEUM SYSTEM

    FDA Adverse Event
    Injury ·BAUSCH AND LOMB·Product code HQC·July 26, 2007

    BSM-6300A

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·October 17, 2018