BEUDAMED
    6 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 ×

    EFAI RTSUITE CT HCAP-Segmentation System

    FDA 510(k)
    FDA Class 2 ·Radiology

    BRAUN THERMOSCAN PRO 4000 SERIES (PROFESSIONAL USE ENVIRONMENT); BRAUN THERMOSCAN IRT 4000 SERIES (HOME USE ENVIRONMENT)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    FREND TSH (REAGENT CARTRIDGE)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    OT VERIO METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 1, 2011

    ABRADER,4.0,EP-1,DSPL BLADE

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code HAB·November 6, 2014

    LIGACLIP** ENDOSCOPIC CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·July 17, 2013