BEUDAMED
    9 results · 20ms · 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 ×

    GUSTILO/RAND TOTAL KNEE SYSTEM (GENESIS)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    GC Initial™

    FDA UDI
    Gc America Inc.·15400556705626·GC Initial™ LF Inside IN-46 Brasil, 20g

    GC Initial™

    FDA UDI
    Gc America Inc.·J0228711461·GC Initial™ LF Inside IN-46 Brasil, 20g

    ORTHOSOURCE

    FDA UDI
    ORTHOSOURCE·D9118711460·Superb Hook Crimp Straight

    Arrow Seldinger Arterial Catheterization Device 18 ga., Arrow Seldinger Arterial Catheterization Device 20 ga., Arrow Seldinger Arterial Catheterization Device 22 ga., Arrow Seldinger Arterial Catheterization Device 24 ga.

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VIDAS B.R.A.H.M.S. PCT ASSAY

    FDA 510(k)
    FDA Class 2 ·Microbiology

    PINNACLE MTL INS NEUT36IDX58OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·June 13, 2014

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·October 15, 2010

    PRECISE BIPOLAR FORCEPS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·December 12, 2012