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.

    CT-MODELLER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    artegral

    FDA UDI
    Merz Dental GmbH·D7091970617·anteriors; shade A3 light; mould BOM

    CANNULATED SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AUDIOMETER, MA30, AIR & BONE CONDUCTION

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    E-CAM COINCIDENCE MODE [510 (K) K970627)

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SYSTEMS, INC., NMG GROUP·Product code IYX·April 20, 2001

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·February 20, 2013

    ACCU-CHEK ® COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·January 25, 2011

    TPS HANDPIECE CORD

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code EIA·July 31, 2014