BEUDAMED
    7 results · 21ms · Sources: EU EUDAMED, US FDA

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    USCI DISP. Y-CONNECTOR W/MODIFIED TUOHY-BORST ADAP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Bioseal Inc.

    FDA UDI
    BIOSEAL·00630094299037·Vaginal Speculum Large

    JETSTREAM G2 SYSTEM, MODELS PV20300 (JETSTREAM G2 CATHETER AND CONTROL POD); PVCN100 (PV CONSOLE)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    REPRODENT

    FDA 510(k)
    FDA Class 2 ·Dental

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·November 3, 2010

    RIATA ACTIVE FIXATION LEAD

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

    PERMANENT CAUTERY SPATULA

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·December 29, 2012