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.

    VAN-TEC FASCIAL DILATOR

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    ONLINE POWDER FREE, LATEX EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    RSCRIBE ELECTROCARDIOGRAPH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GRANUFLO

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·May 8, 2014

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LGW·November 6, 2012

    DEEP BRAIN STIMULATOR/SOLETRA

    FDA Adverse Event
    Injury ·MEDTRONIC·Product code MHY·August 27, 2010