BEUDAMED
    9 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.
    Filters Regulation: Us FDA ×

    AEYE-DS

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    AEYE-DS RETINA SCREENING

    FDA Adverse Event
    Injury ·AEYE HEALTH INC.·Product code PIB·January 22, 2025

    NEXT Medium Fruit Variety Prophy Paste Box 200

    FDA UDI
    Preventech·D024221183·NEXT Medium Fruit Variety Prophy Paste Box of 2...

    COMPREHENSIVE REVERSE SHOULDER - E1 POLYETHYLENE CLAIMS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Vortex Radial Spray Catheter

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

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 31, 2024

    ENDO GIA

    FDA Adverse Event
    Malfunction ·COVIDIEN UNITED STATES SURGICAL CORPORATION·Product code GDW·October 23, 2008

    TRIDENT PSL HA CLUSTER 48MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·August 17, 2011

    EXPRESS® LD ILIAC / BILIARY

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIO·July 11, 2013