BEUDAMED
    8 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.

    STERILIZER, STEAM, CASTLE 3000

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BOSS Instruments

    FDA UDI
    BOSS INSTRUMENTS, LTD., INC.·00888515198821·Perio Elev, 13mm str edge cvd bld, shp, 7 1/4"

    6770372

    FDA Adverse Event
    Malfunction ·August 7, 2017

    SpiralTech Dental Implant System

    FDA 510(k)
    FDA Class 2 ·Dental

    GOPHER 2F SUPPORT CATHETER, MODEL 5600 AND GOPHER 3F SUPPORT CATHETER, MODEL 5610

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VASOVIEW HEM25088284OPRO

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·January 21, 2014

    BIOARC SLING SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·October 1, 2012

    RESTOR IOL

    FDA Adverse Event
    Other ·ALCON RESEARCH LTD·Product code MFK·July 20, 2010