BEUDAMED
    7 results · 26ms · 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.

    TECNOTOMO

    FDA 510(k)
    FDA Class 2 ·Radiology

    discovery®

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011790132000·discovery® Bracket, + 14° Torque, + 8° Angulati...

    MAXMORESPINE SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Torqr Intracardiac Electrode Catheter, Soloist Intracardiac Electrode Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PRIMEADVANCED

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 5, 2014

    REVEAL XT

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code DSI·October 15, 2012

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 22, 2015