BEUDAMED
    8 results · 20ms · 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.

    SURGICAL BLADES

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    WAVE O SPINAL SYSTEM

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169244597·CAGE 2761322 WAVE O 13MM X 22MM 6DEG

    CT CoPilot

    FDA 510(k)
    FDA Class 2 ·Radiology

    PORCELAIN PRIMER

    FDA 510(k)
    FDA Class 2 ·Dental

    CANNULATED 4.0MM HEXAGONAL SCREWDRIVER

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HXX·January 24, 2023

    INSIGNIA

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·April 21, 2014

    ACCU-CHEK COMPACT TEST DRUM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 20, 2007

    PROFEMUR(R) MODULAR FEMORAL NECK

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LWJ·September 26, 2012