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.

    DUNN VESSEL OCCLUDER-STERILE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Crimpable Stop

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746147104·ARCH STOP CRIMPABLE 1MM 030 ROUND 100/PKG

    POCKET TRANSCRANIAL AND VASCULAR DOPPLER SPECTRUM ANALYZER, MODEL 500P; PW DOPPLER ULTRAOUND PROBE, MODEL 2MPB.

    FDA 510(k)
    FDA Class 2 ·Radiology

    Revision Femoral Stem

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·October 4, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 29, 2012

    WHITESTAR SIGNATURE SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MEDICAL OPTICS·Product code HQC·June 5, 2014

    GLOBAL UNITE STD STEM SZ 10 Part Number: 110010100

    FDA Enforcement
    Class II ·Terminated·DePuy Orthopaedics, Inc.·January 19, 2022