BEUDAMED
    7 results · 35ms · 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.

    QuietLab Pro

    FDA 510(k)
    FDA Class 2 ·Dental

    ASAHI Gladius Mongo18 PV ES

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PYXIS 3D Titanium Cage System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TELIGEN IS-1/DF-1 - DR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·November 11, 2008

    FOLEY CATHETER INSERTION TRAY KIT

    FDA Adverse Event
    Malfunction ·MEDIKMARK INC.·Product code FCM·August 11, 2011

    GYNECARE TVT ABBREVO CONTINENCE SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·July 30, 2013

    5.5 EXP VERSE SCR 6.0X50

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SàRL CH·Product code NKB·September 18, 2020