BEUDAMED
    7 results · 21ms · 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.

    DYNAREX SUCTION CATHETERS & KITS

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    GAYHEART CORNEAL EXCISION DEVICE

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    MD211G3 21.3 DIAGNOSTIC IMAGING LCD MONITOR

    FDA 510(k)
    FDA Class 2 ·Radiology

    ACCESS® TOXO IGG

    FDA Adverse Event
    BECKMAN COULTER, INC.·Product code LGD·February 17, 2012

    MINICAP

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·January 18, 2013

    SPRINT QUATTRO

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 13, 2010

    WELLFLEX BILIARY RX STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code FGE·July 9, 2014