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 ×

    MCCUTCHEN ACETABULAR CUP PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    E-CUBE 8

    FDA 510(k)
    FDA Class 2 ·Radiology

    ORTHO T. CRUZI ELISA TEST SYSTEM

    FDA 510(k)
    FDA Class 1 ·Microbiology

    6800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 15, 2014

    RESUSCITAIRE

    FDA Adverse Event
    Malfunction ·DRAGER MEDICAL SYSTEMS, INC. (PNC)·Product code FMT·October 12, 2010

    PARADIGM INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LZG·December 13, 2012

    DURASUL, ALPHA INSERT, JJ/36

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code LZO·March 29, 2017