BEUDAMED
    8 results · 25ms · 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 ×

    S dispensing line

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SIMPLYGO HANDS FREE BREAST PUMP

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

    FLEXTIME FAST & SCAN PUTTY, FLEXTIME FAST & SCAN LIGHT FLOW, FLEXTIME FAST & SCAN MEDIUM FLOW

    FDA 510(k)
    FDA Class 2 ·Dental

    EEA XL 21MM STAPLER WITH 3.5MM STAPLES

    FDA Adverse Event
    Injury ·NORTH HAVEN - USS·Product code GDW·October 8, 2008

    PELVITEX POLYPROPYLENE MESH

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION·Product code FTL·May 1, 2013

    U BY KOTEX CLICK TAMPONS

    FDA Adverse Event
    Malfunction ·QINGDAO P&B CO LTD·Product code HEB·June 17, 2011

    MYNXGRIP VASCULAR CLOSURE DEVICE 6F-7F

    FDA Adverse Event
    Malfunction ·CORDIS SANTA CLARA·Product code MGB·January 7, 2020

    Zimmer Biomet Comprehensive Segmental Revision System (SRS). Orthopedic implants for Proximal Humeral Reconstruction, Distal Humeral Reconstruction, and Total Humeral Reconstruction

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 4, 2018