BEUDAMED
    8 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 ×

    ERIKA ART LI, 3-9621-8, 22-6, 23-4 & VEN 9714-1

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

    Shoreline ACS

    FDA UDI
    Seaspine Orthopedics Corporation·10889981140311·9mm, Locking Cover, Backup

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209121335·

    DIGITAL HAND DYNAMOMETER, MODEL SH5003; DIGITAL PINCH GAUGE, MODEL SH5006

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LOGIQ E9, LOGIQ E9 XDClear 2.0

    FDA 510(k)
    FDA Class 2 ·Radiology

    GREENLIGHT HPS BPH FIBER OPTIC

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·June 5, 2014

    TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·October 4, 2010

    *

    FDA Adverse Event
    Malfunction ·SYNTHES (USA) PRODUCTS LLC·Product code HWC·November 20, 2012