BEUDAMED
    8 results · 26ms · 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 ×

    MICRO-AIRE PULSE LAVAGE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GC Initial™

    FDA UDI
    Gc America Inc.·J0228745041·GC Initial™ Ti Powder Opaque OA3.5, 50g

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756017855·WRIST SPLINT

    SARTORIUS MINISART SM 16596HY

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ESKA JONAS SILICON-SILVER PENILE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PLM MICDP NITRO OL

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·April 22, 2014

    CONTOUR USB

    FDA Adverse Event
    Malfunction ·BAYER HEALTHCARE LLC·Product code NBW·December 14, 2012

    SHUNT SENSOR SYS500

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·October 15, 2010