BEUDAMED
    6 results · 18ms · 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 ×

    HEYER-SCHULTE(R) ONE PIECE SHUNT VENT. CATH. INTRO

    FDA 510(k)
    FDA Class 1 ·Neurology

    SPIROTECH 300

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    IOLMaster 700

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    MINICAP EXTEND LIFE PD TRANSFSET W/TWIST CLAMP EAST EUROPE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·October 19, 2010

    NITE GUARD

    FDA Adverse Event
    Malfunction ·RANIR, LLC·Product code OBR·March 25, 2014

    DEPUY ASR XL FEM IMP SIZE 55

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·December 14, 2012