BEUDAMED
    6 results · 17ms · 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.

    P1OP2B OR P1O92T

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

    CENTRAL VENOUS PRESSURE MANOMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DSL ANDROSTENDIONE RIA (DSL #4200)

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code DXY·February 11, 2013

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·January 10, 2011

    CAMINO ICP MONITORING CATHETER W/INTEGRATED LIC

    FDA Adverse Event
    Injury ·INTEGRA NEUROSCIENCES CA/USA·Product code GWM·July 18, 2014