BEUDAMED
    6 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.

    OMRON TRAVEL TOOTHBRUSH/PLAQUE REMOVER #HT-B005

    FDA 510(k)
    FDA Class 1 ·Dental

    ZEPHYR INFUSION CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AMERLITE MAB FT4 ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    PINNACLE MULTIHOLE II CUP 54MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWA·January 23, 2013

    REVEAL DX

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code DSI·December 14, 2010

    TENDRIL DX

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 10, 2014