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 ×

    CERVEX-BRUSH

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

    Patterson

    FDA UDI
    PATTERSON DENTAL SUPPLY, INC.·D6620708908481·POINT, PAPER, ENDODONTIC

    PREMIER STERILE SALINE WOUND WASH, MODELS 210 ML, WWM

    FDA 510(k)
    FDA Class 2 ·General Hospital

    JUSHA-M550G/ JUSHA-M550/M550G/M550 LCD Monitor

    FDA 510(k)
    FDA Class 2 ·Radiology

    VERTEBRAL BODY STENT-SMALL

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code NDN·December 15, 2022

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·June 11, 2014

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·October 28, 2010

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORP.·Product code MVK·November 21, 2012