BEUDAMED
    8 results · 18ms · 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 ×

    PHARYNGEAL SALIVARY BYPASS TUBE

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111116·KATENA INSTRUMENT RACK

    Instrument Case

    FDA UDI
    KATENA PRODUCTS, INC.·00841668111079·SILICONE MAT FOR K 9-2330

    AMPLIVUE C. DIFFICILE ASSAY

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ASYRA

    FDA 510(k)
    FDA Class 2 ·Neurology

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·January 22, 2013

    SOFTCLIX® LANCET DEVICE

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·December 13, 2010

    TENDRIL ST

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014