BEUDAMED
    10 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    OLYMPUS PBD STENTS

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

    LP Low Profile

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746089152·DB BKT LP 6.5MM LANG UR CUSP 022 T-3 A+10 R=0

    Integra® Miltex®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780415008·Integra® Miltex® Schamberg Comedone Extractor, ...

    SeaSpine Spacer System - Ventura™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981033194·Ventura Trial, 9mm x 28mm x 7mm

    STALIF C(R)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARIOL

    FDA 510(k)
    FDA Class 2 ·Hematology

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·September 3, 2021

    ANIMAS VIBE SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code OYC·July 22, 2015

    SPACE LABS ULTRAVIEW SL PATIENT MONITOR

    FDA Adverse Event
    Malfunction ·SPACELABS HEALTHCARE·Product code DSI·December 15, 2010

    LIFECARE

    FDA Adverse Event
    Malfunction ·HOSPIRA, INC.·Product code MEA·December 31, 2012