BEUDAMED
    9 results · 19ms · 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.

    ADVIA Centaur HAV total assay

    FDA 510(k)
    FDA Class 2 ·Microbiology

    TRULIGHT 5520 AND TRULIGHT 5320

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    POLYTECH PULMONARY FUNCTION FILTER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    PENUMBRA SYSTEM ACE 64 REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·February 4, 2016

    T7 DRIVER CANN AO

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code LXH·July 14, 2016

    PENUMBRA SYSTEM ACE 64 REPERFUSION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code NRY·December 1, 2015

    SECURE 3 MED/SURG BEDOBS 01/13

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·June 3, 2013

    PINN MAR NEUT 32IDX58OD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·June 23, 2011

    ONE TOUCH ULTRA METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·August 27, 2008