BEUDAMED
    8 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.
    Filters Regulation: Us FDA ×

    STAIR-LIFT

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Polystar Selection EDITION

    FDA UDI
    Merz Dental GmbH·D7091981486·anteriors; shade BL3; mould CL2

    STERI-VAC POWER UNITS

    FDA 510(k)
    FDA Class 1 ·Dental

    DEKA Motus AY

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

    LIFEPAK(R) 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·February 27, 2013

    DIAGNOSTIC CATHETER FIXED CURVE WOVEN QUAD

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC EP·Product code DRF·July 25, 2014

    8800

    FDA Adverse Event
    Malfunction ·GE MED SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·February 1, 2011

    DEKA MOTUS AY

    FDA Adverse Event
    Injury ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·February 18, 2019