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.
    Filters Regulation: Us FDA ×

    PILLING WECK M-20 DISPOSABLE AUTOMATIC HEMOCLIP

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

    CMI VACUUM PUMP

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    BIO-STAT III PLATE WASHER

    FDA 510(k)
    FDA Class 1 ·Microbiology

    PROFEMUR(R) Z STEM

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LPH·February 5, 2013

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 3, 2011

    ANIMAS VIBE

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

    BD PYXIS¿ MEDSTATION¿ ES

    FDA Adverse Event
    Malfunction ·CAREFUSION 303, INC.·Product code BRY·March 31, 2025

    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