BEUDAMED
    8 results · 20ms · 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 ×

    Walking rehabilitation training electric wheelchair (ZW518)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    ClariPulmo

    FDA 510(k)
    FDA Class 2 ·Radiology

    Apyx

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

    ALARIS SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION SD·Product code FRN·November 9, 2023

    LIFESTENT FLEXSTAR XL BILIARY STENT

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK·Product code FGE·November 24, 2008

    DUROM ACETABULAR COMPONENT 52/46 CODE L

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·September 1, 2011

    POWERED PATIENT ROTATION BED

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code IKZ·July 23, 2013

    Optical Access System; 5mm x 100mm and 12mm x 100mm; Model #: CTR03 and CTR73. Indicated for use to establish a port of entry fro endoscopic instruments in patients requiring minimally invasive surgical procedures including thoracic, gynecologic laparoscopy and other abdominal procedures.

    FDA Enforcement
    Class II ·Terminated·Stryker Sustainability Solutions·July 1, 2015