BEUDAMED
    9 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 ×

    LIQCRYLIC PRO DENTAL RESIN

    FDA 510(k)
    FDA Class 2 ·Dental

    ReBOSSIS85

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VECTORVISION HIP AND HIP SR

    FDA 510(k)
    FDA Class 2 ·Neurology

    STERIS SYSTEM 1E

    FDA Adverse Event
    STERIS CORPORATION - HOPKINS·Product code MED·February 21, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code FNL·December 30, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 1, 2014

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·September 9, 2016

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·September 12, 2016

    DA-400CIII

    FDA Adverse Event
    Injury ·NAKANISHI INC. (NSK)·Product code EGS·May 26, 2015