BEUDAMED
    6 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.
    Filters Regulation: Us FDA ×

    CONMED UNIVERSAL PLUS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    OPTEC 2300 AFVT, ARMED FORCES VISION TESTER

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    010 HI-TOR INTER/STAND GUIDWIRE PRESHAPE TIP/MODIF

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    APEX MONORAIL

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·December 21, 2010

    TRIOLOGY O2

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC.·Product code CBK·January 23, 2013

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·July 15, 2014