BEUDAMED
    9 results · 19ms · 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.

    NEWPORT CERVICAL MANIPULATOR

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110911·SQUEEZE HANDLE CLEANING TUBE

    equilibrium®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011891350010·10 case-ass.equilibrium® 2 McLaughlin 18 Brac...

    ESTECH HAWKEYE INTRODUCER SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    ACTIVE® Free Testosterone RIA

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    MULTI-LINK RX VISION CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MAF·June 24, 2014

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·November 2, 2010

    VASOVIEW HEMOPRO 2

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·December 21, 2012

    ONE TOUCH ULTRAMINI METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·October 23, 2009