BEUDAMED
    11 results · 21ms · 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 ×

    HEXA100 (hexafocon A) Daily Wear Contact Lenses

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    UHEAD

    FDA UDI
    Stryker GmbH·00886385013503·Head Trial; Size 3

    DA VINCI FLUORESCENCE IMAGING VISION SYSTEM, MODEL FF 100

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    .DECIMAL APERTURE

    FDA 510(k)
    FDA Class 2 ·Radiology

    BELLAFILL DERMAL FILLER

    FDA Adverse Event
    Injury ·SUNEVA MEDICAL, INC.·Product code LMH·November 30, 2017

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 17, 2024

    ANEUVYSION DNA PROBE KIT, 30 ASSAY IVD

    FDA Adverse Event
    Death ·ABBOTT MOLECULAR, INC.·Product code MAO·December 16, 2009

    5.0MM LOCKING SCREW

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·July 8, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·June 14, 2013

    TAXUS® LIBERTÉ®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·October 14, 2014

    INVISION¿ TOTAL ANKLE SYSTEM

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY INC·Product code HSN·July 18, 2022