BEUDAMED
    7 results · 22ms · 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 ×

    IceCap product line

    FDA 510(k)
    FDA Class 2 ·Neurology

    DermaV Laser System

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

    TENS&EMS STIMULATOR (Model: KRES100D, KRES1010, KRES1020, KRES1080)

    FDA 510(k)
    FDA Class 2 ·Neurology

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 9, 2023

    ONE TOUCH ULTRA METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·November 24, 2008

    DUROM ACETABULAR COMPONENT 52/46 CODE L

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code KWA·August 30, 2011

    TOTAL ASR ACET IMP SIZE 50

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KWA·July 23, 2013