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 ×

    CONELOG Titanium base CAD/CAM

    FDA 510(k)
    FDA Class 2 ·Dental

    E.M Adams co, inc.

    FDA UDI
    E.M. ADAMS, INC.·18100013401630·SINGLE INSTRUMENT

    E.M Adams co, inc.

    FDA UDI
    E.M. ADAMS, INC.·10840200301630·SINGLE INSTRUMENT

    ARTHREX BIO-CORKSCREW FT SUTURE ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MULTIPLE NAME

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 29, 2011

    IDENTITY XL DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC. CRMD·Product code DXY·January 13, 2014

    IMPAX CV DICOMSTORE WITH MEDIA PURGE DAEMON (MPD)

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·June 3, 2013