BEUDAMED
    9 results · 30ms · 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 ×

    R2P Navicross

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    24M - Southwest Gas Corp

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588010441·24M - Southwest Gas Corp

    Symmetry Surgical

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482001318·Symmetry® Curette, Spinal, Straight, Size 1, 8 ...

    ATAC PAK URIC ACID REAGENT AND ATAC CALIBRATOR

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SENSICARDIAC MOBI DIAGNOSTIC HEART MURMUR APPLICATION

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BRAVO

    FDA Adverse Event
    Malfunction ·ARIZONA DEVICE MANUFACTURING·Product code FFT·October 30, 2008

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code MDS·July 19, 2011

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 12, 2013

    LIBERTY CYCLER SET, SINGLE CONN./EXT. DL

    FDA Adverse Event
    Malfunction ·REYNOSE MANUFACTURING·Product code FKX·August 19, 2011