BEUDAMED
    7 results · 24ms · 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 ×

    BECKER EXTERNAL DRAINAGE/MONITOR SYS LUMBAR CATH.

    FDA 510(k)
    FDA Class 2 ·Neurology

    K2-HF ENAMEL, powder E-59, 50g.

    FDA UDI
    Yeti Dentalprodukte GmbH·EYET38623030·

    FRAXEL II SR LASER SYSTEM

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

    REDAPT Sleeved Monolithic Revision Stems

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CAPSURE SP NOVUS

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·June 10, 2014

    CHIOCE GUIDEWIRE

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MIAMI·Product code DQX·October 8, 2010

    PARKER BATH

    FDA Adverse Event
    Malfunction ·ARJO HOSPITAL EQUIPMENT AB·Product code ILJ·November 29, 2012