BEUDAMED
    9 results · 28ms · 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 ×

    Okami Medical LOBO Vascular Occlusion System

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Sonic

    FDA UDI
    Sonic Innovations, Inc.·05711583032795·ET40, KIT 10 85 PB BE ENCHANT 40

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776191627·LLETZ LATERAL RETR REG

    De Soutter Medical

    FDA UDI
    DE SOUTTER MEDICAL LIMITED·05051471122833·K-WIRE - DOUBLE TROCAR 0.8mm DIA x 75mm

    EXTEND FRAME SYSTEM, MODEL 1009633

    FDA 510(k)
    FDA Class 2 ·Radiology

    VELSCOPE VX

    FDA 510(k)
    FDA Class 2 ·Dental

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·October 7, 2008

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 4, 2011

    CAST CUTTER

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-KALAMAZOO·Product code HAB·June 27, 2013