BEUDAMED
    8 results · 25ms · 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.

    CLM LARYNGOSCOPE

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    3M™ Victory Series™

    FDA UDI
    3M UNITEK CORPORATION·00652221116451·3M™ Victory Series™ First Molar Bands, 953-179,...

    EMDS ALBUMIN (ALB) TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    VICKERS ERGOMATIC MICROSUR INSTRU-UNIV R O L HAND

    FDA 510(k)
    FDA Class 1 ·Neurology

    PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·RICE CREEK MFG·Product code DXY·February 9, 2013

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·January 7, 2011

    ELLIPSE DR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·July 23, 2014

    CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026