BEUDAMED
    8 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 ×

    SPECTRUM DESIGNS MEDIAL MALAR IMPLANT

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

    DeltaForm HD

    FDA UDI
    Merz Dental GmbH·D7091980140·DeltaForm HD upper posteriors, XL, D3 -MADE IN ...

    LAURIMED SPINAL INJECTION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ProFlex Laser Fibers

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

    UNKNOWN

    FDA Adverse Event
    WILLIAM COOK EUROPE·Product code DTK·October 27, 2015

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 5, 2014

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·February 27, 2013

    MRI PLASTIC PORT WITH ATTACHABLE 8 FR GROHSONG CATHETER - INTROD

    FDA Adverse Event
    Death ·C.R. BARD, INC. (BASD)·Product code LJT·February 1, 2011