BEUDAMED
    8 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.
    Filters Regulation: Us FDA ×

    ORBIC* SPHERICAL ALLOY

    FDA 510(k)
    FDA Class 2 ·Dental

    ERA® Implant Abutment Micro Ang. Base, 3mm Cuff (AN)

    FDA UDI
    STERNGOLD DENTAL LLC·00841549104985·Implant retained overdentures are an establishe...

    PORTA AURIUM, MODEL 2067

    FDA 510(k)
    FDA Class 2 ·Dental

    SHEATHES ULTRASOND GEL

    FDA 510(k)
    FDA Class 2 ·Radiology

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2015

    UNICEL® DXC 600I SYNCHRON® ACCESS® CLINICAL SYSTEM

    FDA Adverse Event
    Injury ·BECKMAN COULTER, INC.·Product code MMI·October 31, 2012

    REALSEAL

    FDA Adverse Event
    Injury ·SYBRONENDO·Product code KIF·May 15, 2014

    DEXTRUS 4137

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVZ·August 11, 2010