BEUDAMED
    6 results · 17ms · 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.

    HEALTH ESSENTIALS MAXI MASSAGER

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    HEART TECHNOLOGY WIRECLIP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SPORICIDIN BRAND DISINFECTANT SOLUTION

    FDA 510(k)
    FDA Class 1 ·General Hospital

    V.A.C.

    FDA Adverse Event
    Injury ·KCI USA INC·Product code OMP·January 17, 2013

    DA+ C SERIES DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code DXY·December 14, 2010

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 10, 2014