BEUDAMED
    7 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.

    MODIFIED LABYSYSTEMS' TOXOPLASMA GONDII IGG EIA

    FDA 510(k)
    FDA Class 2 ·Microbiology

    FORZA

    FDA UDI
    Orthofix US LLC·18257200077083·MONOLITHIC TAMP - 10MM

    SPI DENTAL IMPLANT INICELL

    FDA 510(k)
    FDA Class 2 ·Dental

    ETEST Piperacillin/Tazobactam (P/T) (0.016/4-256/4 ug/mL)

    FDA 510(k)
    FDA Class 2 ·Microbiology

    PRECISION CARTG(18.3X1.33X105)

    FDA Adverse Event
    Injury ·STRYKER INSTRUMENTS-KALAMAZOO·Product code GFA·June 24, 2014

    TERUMO CDI 540 CALIBRATOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DRY·October 22, 2010

    RIATA ACTIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·December 28, 2012