BEUDAMED
    7 results · 18ms · 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 ×

    INTERFACE MODULE IDDD

    FDA 510(k)
    FDA Class 1 ·Cardiovascular

    ALCATEL-LUCENT TELEHEATH MANAGER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Powder Free Nitrile Patient Examination Gloves, Non-Sterile (Orange)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ARTICUL/EZE BALL 28 +8.5 BL

    FDA Adverse Event
    Injury ·8010379 DEPUY INTL., LTD.·Product code JDI·March 7, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 15, 2011

    PROTECTA XT CRT-D

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·August 8, 2014

    Picasso/Picasso Lite lasers Intended use: Dentistry.

    FDA Recall
    Terminated ·AMD Lasers, LLC·Product code GEX·April 15, 2010