BEUDAMED
    8 results · 18ms · 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 ×

    CODMAN-MEDOS VALVE SHUNT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Neurology

    VISTA GRAPH POLYSOMNOGRAPHY AMPLIFIER

    FDA 510(k)
    FDA Class 2 ·Neurology

    BIOSEARCH GLASER PEG PERCUTANEOUS ENDOSCOPIC GASTR

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

    CARBIDE BUR CAVITY ROUND FG012

    FDA Adverse Event
    Malfunction ·MAILLEFER INSTRUMENTS HOLDING SARL·Product code EJL·April 17, 2026

    WECK HEMOCLIP, M20

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code FZP·December 6, 2010

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·February 5, 2013

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 18, 2014

    Angiotech Prostate Stabilization Set. Prostate Stabilization Set. STERILE. Product Number: 500118200. 510k K944522. Qty Dist. - 4,180. MEDICAL DEVICE TECHNOLOGIES, INC. 3600 Southwest 74th Avenue, Gainesville, Florida 32608 U.S.A. Intended Use: Prostate Stabilization Set

    FDA Recall
    Terminated ·Medical Device Technologies, Inc.·Product code IWJ·September 1, 2009